From owner-biophysics@net.bio.net Thu May 01 23:00:00 1997
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From: Jesper Broendum Nielsen <jesper@newton.foodsci.kvl.dk>
Newsgroups: bionet.structural-nmr,bionet.molec-model,sci.med.laboratory,bionet.biophysics,sci.physics
Subject: Announcement: NMR Database at http://newton.foodsci.kvl.dk
Date: Thu, 01 May 1997 09:45:36 +0200
Organization: Royal Veterinary & Agricultural U., Copenhagen, Denmark
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Dear colleges

We have put together a database of publications (incl. abstracts) in low
resolution NMR. The database is separated in two groups of applications:

 - Food Applications
 - Related Applications

Visit:

http://newton.foodsci.kvl.dk

best regards

-- 
~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
  Jesper Broendum, M.Sc. Image Analysis

  Food Technology       and   SFK-Technology A/S  
  Vet. and Agri. Uni.
  Rolighedsvej 30             Vandtaarnsvej 77
  1958 Frederiksberg C        2860 Soeborg, DK
  Ph: (+45) 3528 3205         (+45) 3167 1527
  Fax: (+45) 3528 3245        (+45) 3167 9227
  E-mail:   jesper@newton.foodsci.kvl.dk
  WWW:      newton.foodsci.kvl.dk/jesper
~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~

From owner-biophysics@net.bio.net Thu May 01 23:00:00 1997
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From: simonson@schlitz.u-strasbg.fr (Thomas Simonson)
Newsgroups: bionet.molec-model,bionet.xtallography,bionet.software-xplor,bionet.software,bionet.biophysics
Subject: Protein Engineering Symposium
Date: 2 May 1997 13:34:31 GMT
Organization: CRC - Universite Louis Pasteur - Strasbourg France
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Dear Colleagues,

We are pleased to announce a one-day symposium in

        Strasbourg, May 30th, 1997, on

"Protein Engineering: from Experiment to Theory and Back".

There are no registration formalities or fee.

The program follows. 

For more information send e-mail to koehl@bali.u-strasbg.fr.

We look forward to seeing you.

Yours sincerely,


Patrice Koehl & Tom Simonson



Program:

9:45--10:00   Introduction
10:00--11:00	A. Sali (Rockefeller University)
		Comparative protein structure modelling for
              genome projects.
11:00--12:00	H. Hellinga (Duke University)
		Rational protein design: theory, experiments and 
              applications.
Break
14:00--15:00	D. Moras (IGBMC, Strasbourg)
		Protein--ligand interactions in nuclear
              receptors of steroid hormones.
15:00--16:00	R. Glockshuber (ETH, Zurich)
		Random circular permutation of proteins: a new
              approach to study protein folding.
Break
16:30--17:30	M. Karplus (Harvard and Strasbourg Universities)
		Molecular recognition: free energy simulations
               and combinatorial ligand design.


-----------------------------------------------------------
Thomas Simonson
Laboratoire de Biologie Structurale,
C.N.R.S., Strasbourg
e-mail: simonson@zinfandel.u-strasbg.fr	

From owner-biophysics@net.bio.net Fri May 02 23:00:00 1997
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From: myers@netaxs.com.NOSPAM (PZ Myers)
Newsgroups: bionet.general,bionet.microbiology,alt.life.universe.everything,talk.origins,bionet.biophysics,sci.physics,comp.ai.genetic,bionet.molbio.evolution
Subject: Re: questions about embryos
Date: Sat, 03 May 1997 09:26:49 -0400
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In article <862648806.30339@dejanews.com>, e904952p@hjc.edu.sg wrote:

> I am a high school student seeking some answers.(Somehow I always seem to
> start my article by saying that)
> Recently I've thinking how can that enormous amount of information all be
> stored in one single embryo. Information describing a fully grown
> organism! In a sense a complete blueprint is in that embryo. How does this
> happen?

BIG question...it'll take a little while to explain it. Got a lifetime to
spend on it? :-)

> I am studying chaos theory and I just learned that very simple dynamic
> system can generate extremely complicated behavior. An example is the
> famous Madelbrot set.(well it's not exactly a dynamic system but the
> message is the same)
> Could it be that what is stored in the embryo is a simple mapping, some
> instructions telling the embryo how to evolve. All the details such as the
> complex network of brain cells simple come about as the embryo blindly
> follows the instruction?
> Of course external feedback also plays an important role.

I'm not sure what you mean by a simple mapping...there's nothing simple
about it, and if by "mapping" you mean a one-to-one correspondence between
a chunk of code and a structure, no, I don't think so. There is no tidy
block of code that is dedicated to instructing neuron X to differentiate
a particular transmitter, and to grow an axon that extends 10 microns and
then turns left. Rather, cells are programmed with a set of properties and
rules that indirectly specify a course of development. A cell may express
a receptor that activates a large set of genes if a ligand is bound, another
set if it is not bound. Whichever set that is activated modifies the ability
of the cell to respond to other signals in the environment, which then 
modify the ability of the cell to respond to more signals, and so on.

The complexity of the nervous system is an emergent property of a progressive
and self-referential modulation of gene activity during development. In 
that sense, it is a lot like the complex dynamic systems modeled on computers.

-- 
Paul Z. Myers
http://fishnet.bio.temple.edu/

From owner-biophysics@net.bio.net Fri May 02 23:00:00 1997
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From: "Benjamin Mikesh" <Benjamin_Mikesh@brown.edu>
Newsgroups: bionet.general,bionet.microbiology,alt.life.universe.everything,talk.origins,bionet.biophysics,sci.physics,comp.ai.genetic,bionet.molbio.evolution
Subject: Re: questions about embryos
Date: 3 May 1997 11:56:15 GMT
Organization: Brown University
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> Recently I've thinking how can that enormous amount of information all be
> stored in one single embryo. Information describing a fully grown
> organism! In a sense a complete blueprint is in that embryo. How does
this
> happen?
> Could it be that what is stored in the embryo is a simple mapping, some
> instructions telling the embryo how to evolve?
> He Feng
> e904952p@hjc.edu.sg

Why, yes, that seems reasonable.  Doesn't it?  Research is going on all the
time to study step-by-step embryonic development.  Breakthroughs are made
constantly in the area of cellular differentiation, which is the hot topic
in embryology these days.  Since the DNA is the same in every single cell
of the body, there really is a finite amount of information which is being
utilized by each cell in a different way -- there must certainly also be a
line of code in the DNA telling each different kind of cell what DNA
sequences to read and what to ignore.

-- Ben M.

From owner-biophysics@net.bio.net Fri May 02 23:00:00 1997
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Date: Sat, 03 May 1997 04:01:18 -0600
From: hefeng@cz3.nus.sg
Subject: questions about embryos
Newsgroups: bionet.general,bionet.microbiology,alt.life.universe.everything,talk.origins,bionet.biophysics,sci.physics,comp.ai.genetic,bionet.molbio.evolution
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I am a high school student seeking some answers.(Somehow I always seem to
start my article by saying that)
Recently I've thinking how can that enormous amount of information all be
stored in one single embryo. Information describing a fully grown
organism! In a sense a complete blueprint is in that embryo. How does this
happen?
I am studying chaos theory and I just learned that very simple dynamic
system can generate extremely complicated behavior. An example is the
famous Madelbrot set.(well it's not exactly a dynamic system but the
message is the same)
Could it be that what is stored in the embryo is a simple mapping, some
instructions telling the embryo how to evolve. All the details such as the
complex network of brain cells simple come about as the embryo blindly
follows the instruction?
Of course external feedback also plays an important role.
Please send your response to: e904952p@hjc.edu.sg  as I don't often have
access to Usenet.
Thank you.
----------------------------
He Feng
e904952p@hjc.edu.sg

-------------------==== Posted via Deja News ====-----------------------
      http://www.dejanews.com/     Search, Read, Post to Usenet

From owner-biophysics@net.bio.net Fri May 02 23:00:00 1997
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Date: Sat, 03 May 1997 03:21:05 -0600
From: hefeng@cz3.nus.sg
Subject: LIFE vs DEATH (seeking answers)
Newsgroups: bionet.general,bionet.microbiology,alt.life.universe.everything,talk.origins,bionet.biophysics
Message-ID: <862647231.29844@dejanews.com>
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Hi! I am a high school student fascinated by the phenomena of life. I've
just discovered the wonder of Usenet so I've been posted a lot recently.
One thing I want to ask is that what exactly happens when life leaves a
living organism. Physically I don't see anything much has happened. We
still got roughly, if not exactly, the same amount of matter there, but
still something must have happened, since it's now dead!
So what is it?
If we consider life as an open system could we say that it's gone though
bifurcation and has 'jumped' to another state which is commonly called
'death'?
Life is certainly a strange phenomena. If we construct a system and throw
in some nutrients and a living organism, some time later we find two
organisms in the system. But if we throw in a DEAD organism, nothing will
happen no matter how long we wait.
Isn't it kind of odd?
Please send in you enlightening responses via email at:
e904952p@hjc.edu.sg
Thank you.
------------------------
He Feng
e904952p@hjc.edu.sg

-------------------==== Posted via Deja News ====-----------------------
      http://www.dejanews.com/     Search, Read, Post to Usenet

From owner-biophysics@net.bio.net Fri May 02 23:00:00 1997
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Date: Sat, 03 May 1997 00:52:04 -0600
From: hefeng@cz3.nus.sg
Subject: I am the high school student
Newsgroups: bionet.molbio.evolution,talk.origins,sci.physics,bionet.biophysics
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Hi! I am the high school student who asked about evolution. For the past
several days I've received many kind and often enlightning responeses.
Here I'd like to thank all of you who bothered to write.
--------------
He Feng
e904952p@hjc.edu.sg

-------------------==== Posted via Deja News ====-----------------------
      http://www.dejanews.com/     Search, Read, Post to Usenet

From owner-biophysics@net.bio.net Fri May 02 23:00:00 1997
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From: danyell laughlin <train3@orca.esd114.wednet.edu>
Newsgroups: bionet.biophysics
Subject: evolution
Date: Sat, 03 May 1997 10:06:14 -0700
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When was the last time you talked to your mothers, your best
friends, husbands, siblings?  You are wasting a lot of time on something
that you can not change.  And something that does not have any chance of
changing your life.  Let it go.  Enjoy the things you can do something
about.

From owner-biophysics@net.bio.net Fri May 02 23:00:00 1997
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From: Uncle Al Schwartz <uncleal@uvic.ca>
Newsgroups: bionet.general,bionet.microbiology,alt.life.universe.everything,talk.origins,bionet.biophysics,sci.physics,comp.ai.genetic,bionet.molbio.evolution
Subject: Re: questions about embryos
Date: Sat, 03 May 1997 08:04:55 -0700
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To: e904952p@hjc.edu.sg
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hefeng@cz3.nus.sg wrote:
> 
> I am a high school student seeking some answers.(Somehow I always seem to
> start my article by saying that)
> Recently I've thinking how can that enormous amount of information all be
> stored in one single embryo. Information describing a fully grown
> organism! In a sense a complete blueprint is in that embryo. How does this
> happen?
> I am studying chaos theory and I just learned that very simple dynamic
> system can generate extremely complicated behavior. An example is the
> famous Madelbrot set.(well it's not exactly a dynamic system but the
> message is the same)
> Could it be that what is stored in the embryo is a simple mapping, some
> instructions telling the embryo how to evolve. All the details such as the
> complex network of brain cells simple come about as the embryo blindly
> follows the instruction?
> Of course external feedback also plays an important role.
> Please send your response to: e904952p@hjc.edu.sg  as I don't often have
> access to Usenet.

Configuration information is evolved by the dynamics of the system, not by 
progressively reading off its genetics.  Genes specify boundary conditions, 
interaction rules, and material supply, then things interactively take off.

It is a perfectly reasonable hypothesis.  As 98+% of the human genome consists of 
introns - DNA not bearing genetic information - there isn't really all that much 
space for information storage compard to the demands of the product.  One could 
see how orbits about strange attractors would be resistant to severe reactivity 
to information contamination, tending to give mostly the same product with mild 
and multiple perturbations.

We are what we are because that is the way things naturally fall together.
Good engineering goes with the flow.

-- 
Alan "Uncle Al" Schwartz
UncleAl0@ix.netcom.com ("zero" before @)
uncleal@uvic.ca       (summer only, cAsE-sensitive!)
http://www.ultra.net.au/~wisby/uncleal.htm
 (Toxic URL! Unsafe for children, Democrats, and most mammals)
"Quis custodiet ipsos custodes?"  The Net!

From owner-biophysics@net.bio.net Fri May 02 23:00:00 1997
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From: president@whitehouse.gov (William A Taylor)
Newsgroups: bionet.general,bionet.microbiology,alt.life.universe.everything,talk.origins,bionet.biophysics
Subject: Re: LIFE vs DEATH (seeking answers)
Date: Sat, 03 May 1997 07:40:04 -0600
Organization: Urmia Institute
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e904952p@hjc wrote:

> Hi! I am a high school student fascinated by the phenomena of life. I've
> just discovered the wonder of Usenet so I've been posted a lot recently.
> One thing I want to ask is that what exactly happens when life leaves a
> living organism. Physically I don't see anything much has happened. We
> still got roughly, if not exactly, the same amount of matter there, but
> still something must have happened, since it's now dead!
> So what is it?
> If we consider life as an open system could we say that it's gone though
> bifurcation and has 'jumped' to another state which is commonly called
> 'death'?
> Life is certainly a strange phenomena. If we construct a system and throw
> in some nutrients and a living organism, some time later we find two
> organisms in the system. But if we throw in a DEAD organism, nothing will
> happen no matter how long we wait.
> Isn't it kind of odd?

I see this as a philosophical question, which will not find many
satisfying responses in this newsgroup as this is mostly a scientific
forum.  Scientific views of life can be called mechanistic which says that
living things are merely a more complex arrangement of matter than
non-living things.  A vitalist view holds that living things are of a
different quality than non-living things.  I think that your answer lies
in the latter which, however, is not the scientific view.

-- 
Bill Taylor, Bill@innocent.com

From owner-biophysics@net.bio.net Fri May 02 23:00:00 1997
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From: Kim Kristensen <train4@orca.esd114.wednet.edu>
Newsgroups: bionet.biophysics
Subject: internet class
Date: Sat, 03 May 1997 17:17:53 -0800
Organization: western washington university
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Test message

From owner-biophysics@net.bio.net Fri May 02 23:00:00 1997
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From: joanne doria <train2@orca.esd114.wednet.edu>
Newsgroups: bionet.biophysics
Subject: class on internet
Date: Sat, 03 May 1997 10:11:32 -0700
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This is a test not to keen on the concept of evolution.

From owner-biophysics@net.bio.net Fri May 02 23:00:00 1997
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From: Kim Kristensen <train4@orca.esd114.wednet.edu>
Newsgroups: bionet.biophysics
Subject: class learning about newsgroup
Date: Sat, 03 May 1997 17:13:12 -0800
Organization: western washington university
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Good luck with your topic, was your interest in this topic generated
from the book "Jurassic Park?"

From owner-biophysics@net.bio.net Fri May 02 23:00:00 1997
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From: Training Account 13 <train13@orca.esd114.wednet.edu>
Newsgroups: bionet.biophysics
Subject: learner
Date: Sat, 03 May 1997 10:03:27 -0700
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Hello, there.  I am a 4th grade teacher taking a class on using the
Internet. I'm quite ignorant to all this, but I'm trying to learn this
at warp speed as our school will be Internet ready by fall.

From owner-biophysics@net.bio.net Fri May 02 23:00:00 1997
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From: Kim Kristensen <train4@orca.esd114.wednet.edu>
Newsgroups: bionet.biophysics
Subject: class on internet
Date: Sat, 03 May 1997 17:14:14 -0800
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This is a test

From owner-biophysics@net.bio.net Fri May 02 23:00:00 1997
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From: "R. colleen Zupancic" <rczupancic@telebyte.com>
Newsgroups: bionet.biophysics
Subject: class on news group practice response
Date: Sat, 03 May 1997 17:04:05 -0800
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Good luck with your project. Was your interest for this topic generate
by "Jurassic Park"?

From owner-biophysics@net.bio.net Fri May 02 23:00:00 1997
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From: Richard Steele <Richard@r832.demon.co.uk>
Newsgroups: bionet.general,bionet.microbiology,alt.life.universe.everything,talk.origins,bionet.biophysics
Subject: Re: LIFE vs DEATH (seeking answers)
Date: Sun, 4 May 1997 00:49:45 +0100
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William A Taylor wrote 
 

>
>e904952p@hjc wrote:
>
>> Hi! I am a high school student fascinated by the phenomena of life. 
[etc
>> Isn't it kind of odd?
>
>I see this as a philosophical question, which will not find many
>satisfying responses in this newsgroup as this is mostly a scientific
>forum.  

Unlike this one which is a wibble forum.

-- 
Richard - Whose nice comfy chair by the fire has a new squeak !

From owner-biophysics@net.bio.net Sat May 03 23:00:00 1997
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From: Alec Cawley <alec@cawley.demon.co.uk>
Newsgroups: bionet.general,bionet.microbiology,alt.life.universe.everything,talk.origins,bionet.biophysics
Subject: Re: LIFE vs DEATH (seeking answers)
Date: Sat, 3 May 1997 23:50:20 +0100
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It was said by William A Taylor that
>
>e904952p@hjc wrote:
>
>> Hi! I am a high school student fascinated by the phenomena of life. I've
>> just discovered the wonder of Usenet so I've been posted a lot recently.
>> One thing I want to ask is that what exactly happens when life leaves a
>> living organism. Physically I don't see anything much has happened. We
>> still got roughly, if not exactly, the same amount of matter there, but
>> still something must have happened, since it's now dead!
>> So what is it?
>> If we consider life as an open system could we say that it's gone though
>> bifurcation and has 'jumped' to another state which is commonly called
>> 'death'?
>> Life is certainly a strange phenomena. If we construct a system and throw
>> in some nutrients and a living organism, some time later we find two
>> organisms in the system. But if we throw in a DEAD organism, nothing will
>> happen no matter how long we wait.
>> Isn't it kind of odd?
>
>I see this as a philosophical question, which will not find many
>satisfying responses in this newsgroup as this is mostly a scientific
>forum.  Scientific views of life can be called mechanistic which says that
>living things are merely a more complex arrangement of matter than
>non-living things.  A vitalist view holds that living things are of a
>different quality than non-living things.  I think that your answer lies
>in the latter which, however, is not the scientific view.


"This" may be a scientific forum to you, but because of the uninhibited
way the original poster has spammed the newsgroups, he has also hit a
completely unscientific wibble group. We shall see what eventuates.
Myself, I think it depends how many empties you have lined up when you
reply. Sober, I am scientific. A few beers, and I begin to marvel at
Life. A few more, and it can't *just* be the chemicals, can it? Just
before unconsciousness, vitalism appears to be the prefiect, and
obviousm, answer to it all.

Alec 

From owner-biophysics@net.bio.net Sun May 04 23:00:00 1997
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From: christw@lexis-nexis.com (Christopher C. Wood)
Newsgroups: bionet.general,bionet.microbiology,talk.origins,bionet.biophysics,bionet.molbio.evolution,comp.ai.genetic,sci.physics,alt.life.universe.everything
Subject: Re: conclution on the question of evolution (He Feng)
Date: 5 May 1997 17:09:53 GMT
Organization: LEXIS-NEXIS, Dayton OH
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In article <862823475.27196@dejanews.com>, hefeng@cz3.nus.sg writes:
|> Hi! I am the high school student who raised the question on evolution.

[ snip.  I liked your summary. ]

|> However, one question remains unanswered.
|> Why life at all?

Why not?

|> Is it ture that once the enviroment gets right, life automatically springs
|> out?

We only have one environment to study.  I believe current research
shows a small handful of hundreds of millions of years between the end
of the planet's bombardment/formation, and the first cells.  If a
process that takes 200,000,000 years can be called "springs out", then
the answer is "so far, yes."

|> If so, what's the agency that causes this to happen?

What is the agency that causes tornadoes, or hurricanes?  The same one
applies in this case.  One ought not be surprised by organization
emerging in an energy flow, in this case of light & heat from the sun
warming one side of the earth, and the earth dumping that heat back
into space on its side opposite the sun.

|> I'd like to thank all those who have kindly shared their knowledge and
|> thoughts with me. They have helped me to gain a valuable insight in the
|> issue.

|> Any commends please post to the newsgroup: talk.origins
|> or send your email to: e904952p@hjc.edu.sg
|> Thank you.
|> -------------------
|> He Feng
|> e904952p@hjc.edu.sg
|> 
|> -------------------==== Posted via Deja News ====-----------------------
|>       http://www.dejanews.com/     Search, Read, Post to Usenet

Chris
-- 
Speaking only for myself, of course.
Chris Wood    christw@lexis-nexis.com   cats@CFAnet.com

From owner-biophysics@net.bio.net Sun May 04 23:00:00 1997
Path: biosci!POLY.BIOCHEM.WISC.EDU!guttman
From: guttman@POLY.BIOCHEM.WISC.EDU (HARRY J. GUTTMAN 608-262-3019)
Newsgroups: bionet.biophysics
Subject: equilibrium talk
Date: 5 May 1997 08:28:16 -0700
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Hello all,


I'd like to give my 2 cents worth on the equilibrium
discussion...I try not to think about evolution it makes
my head hurt (from expansion?)

My bias on this is that I am using thermo
and stat mech to describe cellular processes in E. coli.
Generally, I think one can argue that something
does not have to be in complete equilibrium to study
its thermo properties.  For example,  diamond is
not the most stable form of carbon (graphite is).
Yet, it is perfectly reasonable to measure various
thermo properties of diamond since the TIME SCALE
of conversion to graphite is much slower than the measurement.


To bolster my point of view, I give the following quote.
The best description of equilibrium I know of
is in Callen "Thermodynamics and an intro to thermo. stat.",
2nd edition, 1985.
I think, Callen is one of the most definitive texts on thermo.


On page 15 he writes:
   "In actuality, few systems are in absolute and true equilibrium.
In absolute equilibrium all radioactive materials would have
decayed completely .....Such processes, which take cosmic times to 
complete, generally can be ignored.  A system that has completed
the relevant processes of spontaneous evolution, and that 
can be described by a reasonably small number of parameters,
can be considered to be in >>metastable equilibrium<<.
Such a limited equilibrium is sufficient for the application
of thermodynamics.
   "In practice the criterion for equilibrium is circular.
>>Operationally, a system is in an equilibrium state if its 
properties are consistently described by thermodynamic theory<<!"


He goes on to say that this circular criterion is not any 
different from that of any other theoretical formulation (his particular 
example is mechanics).  

Hope this adds something....



Wishing you the best of goodbyes....


Harry J. Guttman



From owner-biophysics@net.bio.net Sun May 04 23:00:00 1997
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From: Richard Steele <Richard@r832.demon.co.uk>
Newsgroups: bionet.general,bionet.microbiology,talk.origins,bionet.biophysics,bionet.molbio.evolution,comp.ai.genetic,sci.physics,alt.life.universe.everything
Subject: Re: conclution on the question of evolution (He Feng)
Date: Mon, 5 May 1997 12:54:02 +0100
Organization: mayonnaise Maker
Distribution: world
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 wrote 
 

>
>Hi! I am the high school student who raised the question on evolution.
>Since then I've received quite a number of responses. I'd like to present
>some of the conclutions of the discussion.
>There are mainly two points.
>First, many who wrote to me pointed out that evolution does NOT
>necessarilly move towards greater complexity.

I'll bet even *more* told you to bog off.  Can't you take a hint?

>I'd like to thank all those who have kindly shared their knowledge and
>thoughts with me. They have helped me to gain a valuable insight in the
>issue.

<INSIGHT>  Another tosser on line  </INSIGHT>

-- 
Richard - Whose nice comfy chair by the fire has a new squeak !

From owner-biophysics@net.bio.net Sun May 04 23:00:00 1997
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Date: Mon, 05 May 1997 05:51:17 -0600
From: hefeng@cz3.nus.sg
Subject: evolution (He Feng e904952p@hjc.edu.sg)
Newsgroups: bionet.general,bionet.microbiology,bionet.biophysics,sci.physics
Message-ID: <862828016.28953@dejanews.com>
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Hi! I realised that I've been missing a lot of discussions. (I couldn't
access Usenet very often, the government won't allow it)
In my article "evolution (please read)" I wrote something about
equilibrim. Certainly living organisms are not in equilibrim state. They
are not even in near-equilibrim state. In such states there will be no
life at all.
But life can't occur in systems that are too far from equilibrim either.
In such circumstance CHAOS takes place and life can't exist. Living
organisms are open sytems (we exchange energy and matter with the outside
world), I understand that it's this constant "kick" from outside world
that keeps us from equillibrim state (which means death!) but not too far.
I am thinking if life itself is a necessary phenomanon, meaning that
natural laws leads inevitably to life, maybe it could be somehow explained
by bifurcation of open systems. When the "kick" from outside reach a
certain critical value, life occurs!
-------------
He Feng

-------------------==== Posted via Deja News ====-----------------------
      http://www.dejanews.com/     Search, Read, Post to Usenet

From owner-biophysics@net.bio.net Sun May 04 23:00:00 1997
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Date: Mon, 05 May 1997 04:33:21 -0600
From: hefeng@cz3.nus.sg
Subject: conclution on the question of evolution (He Feng)
Newsgroups: bionet.general,bionet.microbiology,talk.origins,bionet.biophysics,bionet.molbio.evolution,comp.ai.genetic,sci.physics,alt.life.universe.everything
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Hi! I am the high school student who raised the question on evolution.
Since then I've received quite a number of responses. I'd like to present
some of the conclutions of the discussion.
There are mainly two points.
First, many who wrote to me pointed out that evolution does NOT
necessarilly move towards greater complexity. Indeed in many
circumstances, the reverse happens. At the beginning of life evolution got
no where else to go but towards higher complexity and organisation. You
can't get simpler than the simplest! However this is not the case as time
goes on.
Second, the only driving force in the process of evolution is survival.
The fittest survives always applies. Most of the time complexity helps
oganisms to sruvive better, but sometimes simplicity helps to. That's why
we see a large variety of living things now. Bacterias are still around
and they are doing pretty well.
As shown by the recently reported lizard experiment, the process of
evolution is faster than many of us think. It's possible, actually likely,
that organs such as the eye could have formed during the years.
(Well, human civilization has existed for thousands of years, have we
changed much by the drastic change of our living enviroment?)

However, one question remains unanswered.
Why life at all?
Is it ture that once the enviroment gets right, life automatically springs
out?
If so, what's the agency that causes this to happen?

I'd like to thank all those who have kindly shared their knowledge and
thoughts with me. They have helped me to gain a valuable insight in the
issue.
Any commends please post to the newsgroup: talk.origins
or send your email to: e904952p@hjc.edu.sg
Thank you.
-------------------
He Feng
e904952p@hjc.edu.sg

-------------------==== Posted via Deja News ====-----------------------
      http://www.dejanews.com/     Search, Read, Post to Usenet

From owner-biophysics@net.bio.net Sun May 04 23:00:00 1997
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From: pingouin@crystal.u-strasbg.fr (Francois JEANMOUGIN)
Newsgroups: bionet.general,bionet.microbiology,alt.life.universe.everything,talk.origins,bionet.biophysics,sci.physics,comp.ai.genetic,bionet.molbio.evolution
Subject: Re: questions about embryos
Followup-To: talk.origins
Date: 5 May 1997 08:37:52 GMT
Organization: IGBMC
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In article <862648806.30339@dejanews.com>,
	hefeng@cz3.nus.sg writes:
[...]
> Could it be that what is stored in the embryo is a simple mapping, some
> instructions telling the embryo how to evolve.[...]

	A simple map.... No, it's a colection of data that is express
under circonstances. THe difficulty is not to decode that data (for us),
it is to understand the mechanisms of interaction between the proteins
and higher structures and the data (the genome). The level of complexity
in interactions, give the level of complexity in evolution (or about).

							Francois.

P.S.: The neural network is NOT coded in the genome. It results of
interactions and stimuli that are interpreted regarding the genome.
P.P.S.: All what I wrote is a big reduction of the reality.
P.P.S.: So much newsgroup? well so FollowUp-To: talk.origins (sorry if
I don't read this group...)
-- 
Francois Jeanmougin
Service de bioinformatique / bioinformatics service
IGBMC BP 163 67404 Illkirch France
tel :(France) 03 88 65 32 71 / (international) (+33) 3 88 65 32 71
e-mail : jeanmougin@igbmc.u-strasbg.fr
"C'est pas parcequ'on monte au banc, qu'il faut descendre a jeun." (Thiefaine)

From owner-biophysics@net.bio.net Sun May 04 23:00:00 1997
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From: Terrance Richard Boyes <tez@pierrot.co.uk>
Newsgroups: bionet.general,bionet.microbiology,alt.life.universe.everything,talk.origins,bionet.biophysics
Subject: Re: LIFE vs DEATH (seeking answers)
Followup-To: alt.life.universe.everything
Date: Mon, 5 May 97 01:33:24 +0100 (BST)
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Alec Cawley (alec@cawley.demon.co.uk) wrote:
> It was said by William A Taylor that
> >e904952p@hjc wrote:
> >
> >> Hi! I am a high school student fascinated by the phenomena of life. I've
> >
> >I see this as a philosophical question, which will not find many

Not a homework question?

> >satisfying responses in this newsgroup as this is mostly a scientific
> >forum.  Scientific views of life can be called mechanistic which says that
> 
Or not...
> 
> "This" may be a scientific forum to you, but because of the uninhibited
> way the original poster has spammed the newsgroups, he has also hit a
> completely unscientific wibble group. We shall see what eventuates.

You're talking about SeKS again aren't you :)

Followup-To: alt.life.universe.everything

-- 
<URL:http://www.pierrot.co.uk/>                                     Team AMIGA
Meader's Law: Whatever happens to you, it will previously have happened to
everyone you know, only more so.



From owner-biophysics@net.bio.net Sun May 04 23:00:00 1997
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From: Chris Colby <colby@biology.bu.edu>
Newsgroups: bionet.general,bionet.microbiology,talk.origins,bionet.biophysics,bionet.molbio.evolution,comp.ai.genetic,sci.physics
Subject: misconception about evolution (response to He Feng)
Followup-To: talk.origins
Date: Mon, 05 May 1997 11:34:46 +0000
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I've trimmed the newsgroups line (slightly) and set follow-ups to
talk.origins.

hefeng@cz3.nus.sg wrote:
 
> Hi! I am the high school student who raised the question on evolution.

> Second, the only driving force in the process of evolution is survival.

This is wrong. Replace "survival" with "reproduction" and you are back
on track. At the very least you are accurately describing natural
selection. Fitness is the reproductive rate of a type of organism
relative to other types in the population. There are many components to
fitness. Survival is one. Fertility, fecundity and sexual attractiveness
are some other important components. The alley cat that runs across the
road, finds mates and leaves offspring is more fit than one who doesn't
run across the raod and find mates. This is true even if the "road
runner" gets run over at an earlier age.

In addition, there are other mechanisms of evolution besides natural
selection; they are: mutation, genetic drift, recombination and gene
flow.

If you'd like to learn more about evolution, check out my "Introduction
to Evolutionary Biology" on the talk.origins web page. (I wrote it when
I was a grad. student studying evolution.) It's at:

http://www.talkorigins.org/faqs/faq-intro-to-biology.html

Chris Colby

From owner-biophysics@net.bio.net Sun May 04 23:00:00 1997
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From: Chris Colby <colby@biology.bu.edu>
Newsgroups: bionet.general,bionet.microbiology,talk.origins,bionet.biophysics,bionet.molbio.evolution,comp.ai.genetic,sci.physics,alt.life.universe.everything
Subject: Re: conclution on the question of evolution (He Feng)
Date: Mon, 05 May 1997 11:40:08 +0000
Organization: Boston University Biology
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Richard Steele wrote:

> >Hi! I am the high school student who raised the question on evolution.
> >Since then I've received quite a number of responses.

> I'll bet even *more* told you to bog off.  Can't you take a hint?

It's a high school kid curious about evolution. Do you have to be such
an asshole? Is it bad to foster kid's interest in biology and science?

> >I'd like to thank all those who have kindly shared their knowledge and
> >thoughts with me.

> <INSIGHT>  Another tosser on line  </INSIGHT>

He's thanking people for responding, and you call him a tosser? Oh, the
irony. Get bent Richard.

> Richard - Whose nice comfy chair by the fire has a new squeak !

Chris Colby

From owner-biophysics@net.bio.net Sun May 04 23:00:00 1997
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From: stufnten <tchowa@sfu.ca>
Newsgroups: bionet.general,bionet.microbiology,talk.origins,bionet.biophysics,bionet.molbio.evolution,comp.ai.genetic,sci.physics,alt.life.universe.everything
Subject: Re: conclution on the question of evolution (He Feng)
Date: Mon, 5 May 1997 15:54:41 -0700
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On Mon, 5 May 1997, Chris Colby wrote:

> It's a high school kid curious about evolution. Do you have to be such
> an asshole? Is it bad to foster kid's interest in biology and science?

No, but could we all stop the crossposting? This thread has sod-all to do
with either life, the universe or....

[...]

As I've said, this ng needs a new name.

stufnten, Toby
Kaufman will suffer
Ich weiss keinen besseren Lebenszweck als am Grossen und Unmoeglichen zu
Grunde zu gehen - FNietzsche


From owner-biophysics@net.bio.net Sun May 04 23:00:00 1997
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From: Chris Colby <colby@biology.bu.edu>
Newsgroups: bionet.general,bionet.microbiology,talk.origins,bionet.biophysics,sci.physics,comp.ai.genetic,bionet.molbio.evolution
Subject: Re: questions about embryos
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Date: Mon, 05 May 1997 17:24:38 +0000
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Uncle Al Schwartz wrote:

>  As 98+% of the human genome consists of
> introns 

The human genome is not ninety-eight percent introns. Roughly three
percent of our genome is coding DNA. The rest is various classes of
repetitive DNA. (Britten and Kohne called them foldback DNA, highly
repetitive DNA and middle-repetitive DNA.) The repetitive DNA may be
localized or dispersed.

Introns are non-coding regions of genes. I don't know what percent of
the genome they take up, but since they are part of genes, I'll guess
less than three percent.

[I grabbed this info from Li and Graur's 1991 book (Molecular
Evolution).]

> Alan "Uncle Al" Schwartz

Chris Colby

From owner-biophysics@net.bio.net Sun May 04 23:00:00 1997
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From: kneep@gwis2.circ.gwu.edu (Antonio Greaney Delgado)
Newsgroups: bionet.general,bionet.microbiology,talk.origins,bionet.biophysics,bionet.molbio.evolution,comp.ai.genetic,sci.physics
Subject: Re: conclution on the question of evolution (He Feng)
Date: 5 May 1997 19:08:07 -0400
Organization: The George Washington University
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Chris Colby  <colby@biology.bu.edu> wrote:
>Richard Steele wrote:
>
>> >Hi! I am the high school student who raised the question on evolution.
>> >Since then I've received quite a number of responses.
>
>> I'll bet even *more* told you to bog off.  Can't you take a hint?
>
>It's a high school kid curious about evolution. Do you have to be such
>an asshole? Is it bad to foster kid's interest in biology and science?

I believe what Richard, in his own inimitable way, is try to say (if I may
be so bold, Richard) is that haphazard crossposting is an annoyance to
people on the Internet who wish to avoid it. This student posted to
several newsgroups that undoubtedly have discussions on this topic. Ours,
(alt.life.universe.everything) doesn't (unless something wierd happens
(which admittedly is more often than not (but that doesn't always mean
that everytime something weird happens we talk about evolution))).

Anyway.

For those of you still posting in response to any of these messages,
please strike "alt.life.universe.everything" from the newsgroup list. So
that we may continue to talk about absolutely nothing of consequence.

Kneep!

P.S. Entropy requires no maintenance.

[Note: Alt.life.universe.everything has already been struck from the ng
list in this post.]
-- 
  

From owner-biophysics@net.bio.net Mon May 05 23:00:00 1997
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From: gans@scholar.nyu.edu (Paul J. Gans)
Newsgroups: bionet.general,bionet.microbiology,talk.origins,bionet.biophysics,bionet.molbio.evolution,comp.ai.genetic,sci.physics,alt.life.universe.everything
Subject: Re: conclution on the question of evolution (He Feng)
Followup-To: bionet.general,bionet.microbiology,talk.origins,bionet.biophysics,bionet.molbio.evolution,comp.ai.genetic,sci.physics,alt.life.universe.everything
Date: 6 May 1997 03:41:02 GMT
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Richard Steele (Richard@r832.demon.co.uk) wrote:
: 
:  wrote 
:  
: 
: >
: >Hi! I am the high school student who raised the question on evolution.
: >Since then I've received quite a number of responses. I'd like to present
: >some of the conclutions of the discussion.
: >There are mainly two points.
: >First, many who wrote to me pointed out that evolution does NOT
: >necessarilly move towards greater complexity.
: 
: I'll bet even *more* told you to bog off.  Can't you take a hint?
: 
: >I'd like to thank all those who have kindly shared their knowledge and
: >thoughts with me. They have helped me to gain a valuable insight in the
: >issue.
: 
: <INSIGHT>  Another tosser on line  </INSIGHT>

Uncalled for. 

     ------ Paul J. Gans  [gans@scholar.chem.nyu.edu]


From owner-biophysics@net.bio.net Mon May 05 23:00:00 1997
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From: Richard Steele <Richard@r832.demon.co.uk>
Newsgroups: bionet.general,bionet.microbiology,talk.origins,bionet.biophysics,bionet.molbio.evolution,comp.ai.genetic,sci.physics,alt.life.universe.everything
Subject: Re: conclution on the question of evolution (He Feng)
Date: Tue, 6 May 1997 07:22:56 +0100
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Christopher C. Wood wrote 
 
>
>We only have one environment to study.  I believe current research
>shows a small handful of hundreds of millions of years between the end
>of the planet's bombardment/formation, and the first cells.  If a
>process that takes 200,000,000 years can be called "springs out", then
>the answer is "so far, yes."

etc ...

>Chris
>-- 
>Speaking only for myself, of course.

And speaking to an awful lot of people who *don't* want to know!

Clear all the ruddy crossposts off this thing!!!

-- 
Richard - Whose nice comfy chair by the fire has a new squeak !

From owner-biophysics@net.bio.net Mon May 05 23:00:00 1997
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From: Richard Steele <Richard@r832.demon.co.uk>
Newsgroups: bionet.general,bionet.microbiology,talk.origins,bionet.biophysics,bionet.molbio.evolution,comp.ai.genetic,sci.physics,alt.life.universe.everything
Subject: Re: conclution on the question of evolution (He Feng)
Date: Tue, 6 May 1997 07:20:53 +0100
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Chris Colby wrote 
 

>Richard Steele wrote:
>
>> >Hi! I am the high school student who raised the question on evolution.
>> >Since then I've received quite a number of responses.
>
>> I'll bet even *more* told you to bog off.  Can't you take a hint?
>
>It's a high school kid curious about evolution. Do you have to be such
>an asshole? Is it bad to foster kid's interest in biology and science?

Of course not.  But he might pay attention to where he's posting all
this luvverly stuff!  

>
>> >I'd like to thank all those who have kindly shared their knowledge and
>> >thoughts with me.
>
>> <INSIGHT>  Another tosser on line  </INSIGHT>
>
>He's thanking people for responding, and you call him a tosser? Oh, the
>irony. Get bent Richard.

Hey wuss!!  Just sod off out of my ng ok?

-- 
Richard - Whose nice comfy chair by the fire has a new squeak !

From owner-biophysics@net.bio.net Mon May 05 23:00:00 1997
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From: Tony Lu <sctlu@kraken.itc.gu.edu.au>
Newsgroups: bionet.biophysics
Subject: Laser Photobiology
Date: Sun, 04 May 1997 14:07:32 -0700
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Hi,


I am interested in knowing how lasers may affect biological oraganism.
Does any one know any applications of lasers in genetic engineering?
Or how lasers affect living cells?


Thanks.

From owner-biophysics@net.bio.net Mon May 05 23:00:00 1997
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From: Alec Cawley <alec@cawley.demon.co.uk>
Newsgroups: bionet.general,bionet.microbiology,talk.origins,bionet.biophysics,bionet.molbio.evolution,comp.ai.genetic,sci.physics,alt.life.universe.everything
Subject: Re: conclution on the question of evolution (He Feng)
Date: Tue, 6 May 1997 22:04:05 +0100
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It was said by Richard Steele that
>Christopher C. Wood wrote 
> 
>>
>>We only have one environment to study.  I believe current research
>>shows a small handful of hundreds of millions of years between the end
>>of the planet's bombardment/formation, and the first cells.  If a
>>process that takes 200,000,000 years can be called "springs out", then
>>the answer is "so far, yes."
>
>etc ...
>
>>Chris
>>-- 
>>Speaking only for myself, of course.
>
>And speaking to an awful lot of people who *don't* want to know!
>
>Clear all the ruddy crossposts off this thing!!!

Richard - you don't speak for everyone. Despite the crosspostedness of
it, I find the sensible replies to a serious, if slightly naive,
question of interest and value. As long as it isn't flaming, it isn't
off topic in alue - but *you* are.

Alec 

From owner-biophysics@net.bio.net Tue May 06 23:00:00 1997
Path: biosci!GOLD.CHEM.HAWAII.EDU!shuilin
From: shuilin@GOLD.CHEM.HAWAII.EDU (Shuilin Niu)
Newsgroups: bionet.biophysics
Subject: cuvette holder
Date: 6 May 1997 20:18:09 -0700
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Hi there:
	Could anybody please tell me where I can buy a compact 
thermoelectric cooled cuvette holder (holds 1.0 x 1.0 cm cuvette) with 
stirring capability? 

From owner-biophysics@net.bio.net Tue May 06 23:00:00 1997
Path: biosci!BIOSCI.CBS.UMN.EDU!cgross
From: cgross@BIOSCI.CBS.UMN.EDU ("Carol Gross")
Newsgroups: bionet.biophysics
Subject: Moderating bionet.biophysics
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It has been proposed that the bionet.biophysics newsgroup be converted to a
moderated newsgroup to avoid inappropriate postings which have been increasing 
on this group.  The purpose of this notice is twofold:  

(1) to solicit volunteers to serve as moderators (without which the status of 
the group will not be changed). If you would be willing to serve as a moderator,
please post a message to Carol Gross at cgross@biosci.cbs.umn.edu.  The 
moderator position may be done on a rotational basis if several people are 
willing to act as moderator.

(2) to determine whether the members of the group agree to such a conversion.  
If you endorse or oppose conversion to a moderated format, discussion should be 
conducted on the bionet.biophysics newsgroup.

The deadline to volunteer for the moderator position is June 1, 1997.


Carol Gross
bionet.biophysics Discussion Leader


****************************************************************
Carol Gross                            cgross@biosci.cbs.umn.edu
Biophysics Internet Coordinator        612-625-5262 (voice)
University of Minnesota                612-625-5780 (fax)
Department of Biochemistry
****************************************************************


From owner-biophysics@net.bio.net Tue May 06 23:00:00 1997
Path: biosci!UABDPO.DPO.UAB.EDU!bch0016
From: bch0016@UABDPO.DPO.UAB.EDU
Newsgroups: bionet.biophysics
Subject: Re: evolution?(please read)
Date: 7 May 1997 08:52:35 -0700
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crs wrote:
> 
> John Gardner wrote:
> >         No FACT of evolution where one species has led
> > to another.  Change within species to an extremely limited
> > degree yes, but nothing that would justify the _miraclulous_
> > transformation of one species into another.
> >
> > --
> >     John Gardner

A believer is believer, you never can convince him to change his mind.


From owner-biophysics@net.bio.net Tue May 06 23:00:00 1997
From: ogr81@nospam.computan.on.ca (Rumple Stiltzski)
Newsgroups: bionet.general,bionet.microbiology,alt.life.universe.everything,talk.origins,bionet.biophysics
Subject: Re: LIFE vs DEATH (seeking answers)
Date: Wed, 07 May 1997 16:09:40 GMT
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Xref: biosci bionet.general:26726 bionet.microbiology:9882 talk.origins:311656 bionet.biophysics:3003

hefeng@cz3.nus.sg wrote:

>Hi! I am a high school student fascinated by the phenomena of life. I've
>just discovered the wonder of Usenet so I've been posted a lot recently.
>One thing I want to ask is that what exactly happens when life leaves a
>living organism. Physically I don't see anything much has happened. We
>still got roughly, if not exactly, the same amount of matter there, but
>still something must have happened, since it's now dead!
>So what is it?
>If we consider life as an open system could we say that it's gone though
>bifurcation and has 'jumped' to another state which is commonly called
>'death'?
>Life is certainly a strange phenomena. If we construct a system and throw
>in some nutrients and a living organism, some time later we find two
>organisms in the system. But if we throw in a DEAD organism, nothing will
>happen no matter how long we wait.


>Isn't it kind of odd?

>Thank you.

>----------

This question has been pondered for centuries, in many scientific (and
otherwise, such as philosophy, theology) forums such as physics,
anthropology, biology etc. and the solution to one question only leads
to a myriad of others.
     I am not a scientist myself, you so can gauge how much
credibility you would like to lend my theory.
     There is a form of light, as of yet undetected by human eye or
aperatus, that dictates a large amount of survival instincts for life
on our planets.  This 'colour' varies in 'hue, depth, degree' etc. and
depending on how certain parts of the brain respond, tell the
biological creature what to do.  For example, there is a hue of
undetected light that tells a bird to fly south; another that drives
the lemmings over cliffs, and another that breaths life into potential
life.
     This light, like all light, is an energy, and it sparks the gap
between existance and non-existance much the way a sparkplug does in a
Renault.
     The knowledge of this light is very muddled at the moment, and
the insinuations of it go by many different names.  Myself, I call it
God for lack of better word.
     Thanx for your time.  Take care.
>He Feng
>e904952p@hjc.edu.sg
>
>-------------------==== Posted via Deja News ====-----------------------
>      http://www.dejanews.com/     Search, Read, Post to Usenet


From owner-biophysics@net.bio.net Wed May 07 23:00:00 1997
Path: biosci!GEOCITIES.COM!gmed
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Subject: FREE HOME PAGE
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FREE MONEY-SAVING, MONEY-MAKING HOMEPAGE! Links to other FREE SERVICES.

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From owner-biophysics@net.bio.net Wed May 07 23:00:00 1997
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From: prm@aber.ac.uk (Pedro Mendes)
Newsgroups: bionet.metabolic-reg,bionet.cellbiol,bionet.molbio.proteins,bionet.biophysics,sci.bio.misc
Subject: 1998 GRC on Macromolecular Organization and Cell Function
Followup-To: bionet.metabolic-reg
Date: 7 May 1997 09:30:10 GMT
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Keywords: conference web page
Xref: biosci bionet.metabolic-reg:1214 bionet.cellbiol:7272 bionet.molbio.proteins:10675 bionet.biophysics:3009 sci.bio.misc:8838

Gordon Research Conference on Macromolecular Organization and Cell Function

September 13-17, 1998, Queen's College, University of Oxford

Chaired by Douglas Kell (Aberystwyth) and John Wilson (Michigan)

Full details (including application form) can be found on:

http://gepasi.dbs.aber.ac.uk/grc98.html


From the conference program:
"The focus of the conference is on the functional organization of cellular 
components, and the critical role of this organization in metabolism and its 
regulation. [...] Conference participants have been especially sensitive to 
the fact that much of this organization may be destroyed, or at least 
grossly perturbed, when studies are performed in vitro. Thus, a persistent 
feature in the conference has been the cautious extrapolation of in vitro 
results to the in vivo condition, as well as development and application of 
techniques that allow one to study cellular structure and function in vivo. 
[...]" 

Check it at http://gepasi.dbs.aber.ac.uk/grc98.html


From owner-biophysics@net.bio.net Thu May 08 23:00:00 1997
Path: biosci!CCIT.ARIZONA.EDU!AYool
From: AYool@CCIT.ARIZONA.EDU (Andrea Yool)
Newsgroups: bionet.biophysics
Subject: Re: Moderating bionet.biophysics
Date: 9 May 1997 08:54:45 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 46
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Message-ID: <01IINRRQB2CY938M8E@CCIT.ARIZONA.EDU>
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>It has been proposed that the bionet.biophysics newsgroup be converted to a
>moderated newsgroup to avoid inappropriate postings which have been increasing
>on this group.  The purpose of this notice is twofold:
>
>(1) to solicit volunteers to serve as moderators (without which the status of
>the group will not be changed). If you would be willing to serve as a
>moderator,
>please post a message to Carol Gross at cgross@biosci.cbs.umn.edu.  The
>moderator position may be done on a rotational basis if several people are
>willing to act as moderator.
>
>(2) to determine whether the members of the group agree to such a conversion.
>If you endorse or oppose conversion to a moderated format, discussion should
>be
>conducted on the bionet.biophysics newsgroup.
>
>The deadline to volunteer for the moderator position is June 1, 1997.



-----------------------------------------------------------
Hi, Carol,

I was planning either to volunteer, or to withdraw from the newsgroup.
With the overwhelming redundancy of the recent set of postings on
evolution, I've decided to withdraw.  I don't think the postings fit into
the category of inappropriate  (as the sex and cash ones are) but
nonetheless they have (for me) strayed beyond relevance to biophysics.
Once the thermodynamic and equilibrium discussion points were made and all
points of view were stated, the subject was sufficiently handled.  Time to
move on.

Andrea Yool


_____/\______________/\______________/\______________/\______________/\_____
     /\      /\      /\      /\      /\      /\      /\      /\      /\
____//\\____//\\____//\\____//\\____//\\____//\\____//\\____//\\____//\\____
    \\//    /  \    \\//    /  \    \\//    /  \    \\//    /  \    \\//
_____\/____/    \____\/____/    \____\/____/    \____\/____/    \____\/_____

ANDREA YOOL    DEPTS OF PHYSIOLOGY AND PHARMACOLOGY    UNIVERSITY OF ARIZONA
____________________________________________________________________________




From owner-biophysics@net.bio.net Thu May 08 23:00:00 1997
Path: biosci!rutgers.rutgers.edu!gatech!news.mathworks.com!news.maxwell.syr.edu!disgorge.news.demon.net!demon!dispatch.news.demon.net!demon!r832.demon.co.uk!r832.demon.co.uk!Richard
From: Richard Steele <Richard@r832.demon.co.uk>
Newsgroups: bionet.general,bionet.microbiology,alt.life.universe.everything,talk.origins,bionet.biophysics,sci.physics,comp.ai.genetic,bionet.molbio.evolution
Subject: Re: questions about embryos
Date: Fri, 9 May 1997 13:17:40 +0100
Organization: mayonnaise Maker
Distribution: world
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krhenry wrote 
 

>Please define what you mean by Embryo.  Are you referring to the fertilized
>egg?  Or  later, multicellular, stages?  

I haven't referred to embryos at all.


I have, however, referred to the irresponsible list of groups that this
moron has crossposted to.

I did, once upon a long time, start my requests for removal of same,
very politely.


I don't feel polite any more.


REMOVE THE FUCKING CROSSPOSTS YOU MORONS!!!

-- 
Richard - Whose nice comfy chair by the fire has a new squeak !

From owner-biophysics@net.bio.net Thu May 08 23:00:00 1997
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From: Smudge <malcolm@bellona.demon.co.uk>
Newsgroups: bionet.general,bionet.microbiology,alt.life.universe.everything,talk.origins,bionet.biophysics,sci.physics,comp.ai.genetic,bionet.molbio.evolution
Subject: Re: questions about embryos
Followup-To: alt.life.universe.everything
Date: Fri, 9 May 1997 12:57:28 +0100
Organization: Izzy wizzy, let's get bizzy.
Distribution: world
Message-ID: <Y8TW8VAoExczEwES@bellona.demon.co.uk>
References: <862648806.30339@dejanews.com>
 <01bc5c22$f9da2d80$4fe386cd@default>
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krhenry <krhenry@sirius.com> shook the scrabble bag and this fell
out.....
>Please define what you mean by Embryo.  Are you referring to the fertilized
>egg?  Or  later, multicellular, stages?  

Please go and find out what 'stop cross-posting' means and then do it.

Thank you.
-- 
Smudge



Follow ups set to ALUE

From owner-biophysics@net.bio.net Fri May 09 23:00:00 1997
Path: biosci!ihnp4.ucsd.edu!munnari.OZ.AU!news.ecn.uoknor.edu!feed1.news.erols.com!news-peer.sprintlink.net!news.sprintlink.net!Sprint!ais.net!news.texas.net!davej
From: davej@sedona.net (Dave Jensen)
Newsgroups: bionet.biophysics
Subject: Bio-career Disussion Forum
Date: Sat, 10 May 1997 09:31:23 -0700
Organization: Search Masters International
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X-Newsreader: Yet Another NewsWatcher 2.3.4

A new, non-commercial career discussion forum is available for your
browsing and posting interests. No commercial posts or spam are allowed on
this news forum, and it is entirely moderated so as to make it 100% worthy
of your contribution.

There are hundreds of posts on dozens of topics of interest to anyone in
the sciences. If you'd like, post your questions and find dozens of other
people who may have had similar experiences and who you can network with or
get some advice from. Already, networking subgroups have sprouted from the
biotechnology section of this career discussion forum.

Here are some topics JUST FROM THE LAST WEEK, and we have hundreds of
archived posts:

Career change to CRA 

Should you mention your advisor as a reference ? 

Best MBA for biotech

Liberal Arts Positions? 

Scientist salaries?

Temporary Placement Firms, any good?

Multiple job offers, maybe?

Salary trends 

Keeping the interview alive...

One worried soon to be graduate.

Changing jobs/employers 



Join our career discussion forum at http://cns.bio.com/hr/forum/


regards,

Dave Jensen, Moderator

From owner-biophysics@net.bio.net Sun May 11 23:00:00 1997
Newsgroups: bionet.biophysics
Path: biosci!ihnp4.ucsd.edu!munnari.OZ.AU!news.ecn.uoknor.edu!feed1.news.erols.com!disgorge.news.demon.net!demon!dispatch.news.demon.net!demon!netcom.net.uk!nntpfeed.doc.ic.ac.uk!sunsite.doc.ic.ac.uk!lyra.csx.cam.ac.uk!hgmp.mrc.ac.uk!ebi.ac.uk!news
From: David Starks-Browning <starksb@ebi.ac.uk>
Subject: Parallel Programming Course at EMBL-Heidelberg
Message-ID: <t3911kh07y.fsf@sol19.ebi.ac.uk>
Sender: starksb@sol19.ebi.ac.uk
Date: Mon, 12 May 1997 21:03:29 GMT
Organization: EBI - European Bioinformatics Institute
X-Newsreader: Gnus v5.3/Emacs 19.34
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		     [please post and distribute]

The Supercomputing Resource for Molecular Biology (SRMB), located at
the European Molecular Biology Laboratory in Heidelberg, is offering
training courses in

	 Parallel Programming and High Performance Computing

to European researchers in molecular biology.  The next course will
be held 8 - 14 June 1997.

The course is an intensive and comprehensive introduction to parallel
programming and high performance computing for European molecular
biologists.  Topics include:

     Heterogeneous distributed computing with PVM 

     Message passing programming with MPI 

     Data parallel programming with Fortran90/HPF 

     Methodologies for designing parallel algorithms 

     Performance modeling and scalability analysis 

     Optimization for modern microprocessors 

     Shared memory programming and parallelizing compilers 

     Case studies from parallel applications in molecular biology 

There is considerable emphasis on hands-on experience through
practical sessions.  In particular, participants will write and
execute their own parallel programs in PVM, MPI and Fortran90/HPF.

The course is open to European researchers at the advanced
post-graduate level who have research interests in molecular biology,
including sequence analysis, image processing, structure refinement,
protein design and molecular dynamics.  Participants from EU countries
will be supported by an EU HCM/ALSF grant.  Residents of other EMBL
member countries will be supported by funds from EMBL. Participants
receive travel, accommodation and a subsistence allowance during their
visit, as well as access to the computational facilities of the
Laboratory.

If you wish to attend you should fill out an online application form
AS SOON AS POSSIBLE.  Further information, with links to a detailed
agenda and application forms, can be found at:

     <http://www.embl-heidelberg.de/Services/srmb/pphpc_course/>

=========================================================================
David Starks-Browning                         | starksb@ebi.ac.uk
Technology Transfer Node Manager              !
European Bioinformatics Institute             !
Wellcome Trust Genome Campus                  ! tel: +44(0)1223-49 46 16
Hinxton, Cambridge CB10 1SD, UK               ! fax: +44(0)1223-49 44 68
=========================================================================

From owner-biophysics@net.bio.net Sun May 11 23:00:00 1997
Path: biosci!biosci!not-for-mail
From: sunger@a.crl.com (Stefan Unger)
Newsgroups: bionet.biophysics,bionet.molec-model
Subject: CONF: 8th Cyprus Conf on New Methods in Drug Research (5/98)
Date: 12 May 1997 16:27:20 -0700
Organization: BioSoftware Marketing
Lines: 86
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <sunger-1205971118150001@a103015.sfo3.as.crl.com>
NNTP-Posting-Host: net.bio.net
Xref: biosci bionet.biophysics:3032 bionet.molec-model:1544

The 8th Cyprus Conference on New Methods in Drug Research
Limassol, Cyprus 
May 4-9, 1998

Conference Executive: 
Chair: Alex Makriyannis (U. Conn. Storrs, USA) 
Committee: N. Castagnoli (USA), J.P. Devlin (USA), U. Hacksell 
(Sweden), L.H. Hurley (USA) and M. Abou-Gharbia (USA)


For the past seventeen years, this classic event has served
as the biennial opportunity for researchers and management
executives to interact, exchange views and philosophies,
preview cutting edge technologies in Drug Discovery and get
a glimpse of things to come. The format is the traditional
Gordon-style enhanced by the historical ambiance of Cyprus!
Both the scientific papers and the interests of the
participants are multidisciplinary and this mix, inevitably,
results in innovative new approaches and collaborations.

Half Day Technical Sessions: 

* New Roles for Synthetic Chemistry in Drug Design (Chair:
Steve Hanessian (U. Montreal))

* Advances in Drug Receptor Research (Chair: Hendrik
Timmerman (Amsterdam Center for Drug Research))

* The Use of Computational, Biophysical and Biochemical
Methods (Chairs: Stephen Fesik (Abbott), Alex Makriyannis
(U. Conn. Storrs))

* Ultra-High Throughput Technologies in Discovery and
Development (Chair: Al Kolb (Packard Instrument))

* Micro- and Nanotechnologies in Measuring Biomolecular
Interactions (Chair: Herman Gaub (Ludwig Maximilians Univ)

* Computational-HTS Integration in Drug Discovery (Round
Table Discussion)

* Genomics-based Approaches in Discovery and
Structure-Function Correlations (Chair: Casey Case
(Tularik))

* Novel Design Approaches in Combating Drug Resistance
(Chair: Lawrence Melvin (Amgen))

Conference Location Time and Registration: 

The Conference will take place from Monday, May 4th 
through Friday, May 9th 1998 at the five-star Hawaii Beach 
Hotel, Limassol, Cyprus. Attendance is restricted to 150 
participants to encourage interaction. Registration fees 
(US $595 per person; US $395 for academics) includes attendance 
at all sessions and morning and afternoon breaks, but not meals. 
Local accommodations and air/ground travel expenses are the 
responsibility of the participant and can be arranged at the time 
of registration. Post conference tours are also available; please inquire.

An important event, both as a refreshing midweek break and
as an opportunity for casual and productive collegial
interactions is the traditional Wednesday excursion to
historical and archeological sites of interest followed by a
memorable evening of Cypriot fare and entertainment.
(Optional with separage charge).

Sponsor: 

The European Federation of Medicinal Chemistry

Contact: 

ARRT International, Inc.,
P.O. Box 1838 
New Milford, CT 06776, USA 
Telephone: 860-355-5195
Facsimile: 860-355-5975
e-Mail: arrtintl@prodigy.net

-- 
Stefan Unger, Ph.D.                                  
BioSoftware Marketing
4151 Middlefield Rd, Ste 109
Palo Alto, CA 94303-4743


From owner-biophysics@net.bio.net Mon May 12 23:00:00 1997
Path: biosci!bcm.tmc.edu!news.msfc.nasa.gov!europa.clark.net!news-peer.sprintlink.net!news.sprintlink.net!Sprint!uunet!in3.uu.net!200.255.218.7!news.unisys.com.br!news
From: "Lysandro Trotta Santos" <lysandro@uninet.com.br>
Newsgroups: alt.paranet.metaphysics,alt.sci.physics.acoustics,alt.sci.physics.new-theories,alt.sci.physics.spam,bionet.biophysics,gac.physics.astronomy,harvard.physics.sps,sci.med.physics,sci.physics,sci.physics.accelerators,sci.physics.computational.fluid-
Subject: MD Technology
Date: 13 May 1997 01:28:26 GMT
Organization: Smart Soft Co.
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Xref: biosci bionet.biophysics:3034 sci.med.physics:5473 sci.physics:212210 sci.physics.accelerators:2890

Hi!

	I'm from Rio de Janeiro, Brazil and I'm searching for some MiniDisk (MD)
information. Anything!!! URLs, emails, newsgroups etc etc... Please, if
someone could help me, send email to lysandro@uninet.com.br.
	I do appreciate your attention.

	Regards from Ipanema!
	Lysandro.

From owner-biophysics@net.bio.net Mon May 12 23:00:00 1997
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Newsgroups: bionet.biophysics
Subject: unsubscribe ...
Message-ID: <337836B8.5BD2@el.utwente.nl>
From: Bas de Heij <heij_s@el.utwente.nl>
Date: Tue, 13 May 1997 11:39:04 +0200
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and an other one bites the dust .... :-(

From owner-biophysics@net.bio.net Mon May 12 23:00:00 1997
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From: regentag9@aol.com (Regentag9)
Newsgroups: bionet.biophysics
Subject: persistence length: a topological parameter of DNA et al.
Date: 13 May 1997 03:35:08 GMT
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Is it possible for a humble biologist to aquire a coherent explanation for
this concept that does not invoke graduate level physics, yet does not
"dumb down" and trivialize it?  


From owner-biophysics@net.bio.net Mon May 12 23:00:00 1997
Path: biosci!HAVERFORD.EDU!jdepaula
From: jdepaula@HAVERFORD.EDU (Julio de Paula)
Newsgroups: bionet.biophysics
Subject: unsubscribe
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From owner-biophysics@net.bio.net Mon May 12 23:00:00 1997
Path: biosci!rutgers.rutgers.edu!gatech!news-out.communique.net!communique!news-spur1.maxwell.syr.edu!news.maxwell.syr.edu!disgorge.news.demon.net!demon!dispatch.news.demon.net!demon!netcom.net.uk!nntpfeed.doc.ic.ac.uk!sunsite.doc.ic.ac.uk!lyra.csx.cam.ac.uk!us1.rhbnc.ac.uk!yama.mcc.ac.uk!news.york.ac.uk!not-for-mail
From: David Scott <djs17@york.ac.uk>
Newsgroups: bionet.biophysics
Subject: Re: persistence length: a topological parameter of DNA et al.
Date: Tue, 13 May 1997 14:01:09 -0700
Organization: University of York. York. Y01 5DD
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Regentag9 wrote:
> 
> Is it possible for a humble biologist to aquire a coherent explanation for
> this concept that does not invoke graduate level physics, yet does not
> "dumb down" and trivialize it?

ok, here goes......

Persitance length is defined as the average projection of the end-to-end 
distance vector, r, on the first bond of the chain, in the limit of 
infinite chain length.....blah,blah,blah...

So in English......

Persitance length is a measure of how long a polymer, such as DNA, 
perists in a certain direction. To give it a (useful) physical meaning, 
the direction of persitance is usually defined as being in the same 
direction as that of the first segment of the chain. So with DNA which is 
quite flexible, the persitance length is only a few 10's of nanometres, 
myosin is much greater, as it is stiffer.
Thats the best I can do, however Biophysical Chemistry by Cantor and 
Schimmel (Freemann, 1980) gives a good, if mathematical introduction.

I hope this helps....

Dave. 

-- 

*********************************
* Dr. David Scott		*
* Dept Biology			*
* University of York		*
* YORK				*
* UK				*
*				*
* phone  +44 1904 432867	*
* fax       +44 1904 432860	*
*********************************

From owner-biophysics@net.bio.net Mon May 12 23:00:00 1997
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Subject: Returned mail: User unknown
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From owner-biophysics@net.bio.net Mon May 12 23:00:00 1997
Path: biosci!MIDWAY.UCHICAGO.EDU!khouamed
From: khouamed@MIDWAY.UCHICAGO.EDU (Khaled Houamed)
Newsgroups: bionet.biophysics
Subject: MOLECULAR NEUROBIOLOGY POSTDOCS U. CHICAGO
Date: 13 May 1997 09:15:48 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
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<smaller>Postdoctoral Positions in Molecular Neurobiology

University of Chicago


Postdoctoral positions are available to: 

1) Perform structure / function studies on recombinant small
conductance calcium activated  potassium channels (SK channels) and,

2) Perform structure / function studies on recombinant G-protein
coupled receptors members of family C (metabotropic glutamate
receptors, calcium sensor, and GABA subB receptor).

Recent Ph.D. graduates in Physiology, Pharmacology, Biochemistry,
Neuroscience, or allied fields, with experience in cell physiology
(patch clamp, oocyte voltage clamp, or fura measurements), or molecular
biology techniques are invited to apply for these positions.  Please
send a current CV including a summary of relevant research experience
and names and addresses of three referees to Dr. K. Houamed at the
address below.


Khaled Houamed Ph.D.

Department of Anesthesia and Critical Care,

Committees on Neurobiology and Cell Physiology

The University of Chicago Medical Center

5841 S. Maryland Ave., Box 4028

Chicago, IL 60637

USA

Tel #    Secretary                      (773) 702-4055

        Office                         (773) 702-7552

        Laboratory              (773) 834-0385       

Fax #                             (773) 702-4791


The University of Chicago is an Affirmative Action, Equal Opportunity
Employer.


</smaller>



From owner-biophysics@net.bio.net Mon May 12 23:00:00 1997
Path: biosci!bcm.tmc.edu!news.msfc.nasa.gov!europa.clark.net!feed1.news.erols.com!howland.erols.net!news2.digex.net!news.intercon.com!news5.digex.net!haven.umd.edu!news.umbc.edu!not-for-mail
From: cweiss1@umbc.edu (Christopher Weiss)
Newsgroups: bionet.biophysics
Subject: Backbone bond angle and length data
Date: 13 May 1997 15:42:59 -0400
Organization: University of Maryland, Baltimore County
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Message-ID: <5lag83$5t2@umbc10.umbc.edu>
NNTP-Posting-Host: umbc10.umbc.edu
NNTP-Posting-User: cweiss1

I need protein backbone bond angle and bond length data.  Not tortional angles.
Angles and lengths needed:
N-terminus H-N-H
N-terminus H-N-C
N-Calpha-H
N-Calpha-C(carboxyl)
O=C-Calpha
O=C-N
H-N-H (in peptide bond)
C-N-Calpha
C-terminus Calpha-C=O
C-terminus Calpha-C-O
C-terminus O=C-O

Did I miss any?

Thanks,
Christopher

From owner-biophysics@net.bio.net Tue May 13 23:00:00 1997
Newsgroups: bionet.biophysics
Path: biosci!ihnp4.ucsd.edu!swrinde!cs.utexas.edu!feeder.chicago.cic.net!su-news-hub1.bbnplanet.com!cam-news-hub1.bbnplanet.com!news.bbnplanet.com!news.maxwell.syr.edu!news.new-york.net!actcom!news
From: Shitka Gohding<hofg@sdfkfjh.com>
Subject: Free XXX
X-Nntp-Posting-Host: jedi14.shani.net
Message-ID: <EA57pw.IDs@actcom.co.il>
Sender: news@actcom.co.il (News)
Organization: Mimimu LTD.
Date: Tue, 13 May 1997 23:25:08 GMT
Lines: 5

Goto:

http://www.geocities.com/soho/lofts/5957/

       Thanks.

From owner-biophysics@net.bio.net Wed May 14 23:00:00 1997
Path: biosci!bcm.tmc.edu!news.msfc.nasa.gov!europa.clark.net!cpk-news-hub1.bbnplanet.com!su-news-hub1.bbnplanet.com!news.bbnplanet.com!news.Stanford.EDU!nntp.Stanford.EDU!not-for-mail
From: Andrew Fell <ahfell@netmatters.co.uk>
Newsgroups: bionet.general,bionet.microbiology,alt.life.universe.everything,talk.origins,bionet.biophysics
Subject: Re: LIFE vs DEATH (seeking answers)
Date: Wed, 14 May 1997 18:00:43 -0700
Organization: Stanford University
Lines: 36
Message-ID: <337A603B.6B7@netmatters.co.uk>
References: <862647231.29844@dejanews.com> <3371a50f.4283648@news.computan.on.ca>
Reply-To: ahfell@netmatters.co.uk
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Xref: biosci bionet.general:26810 bionet.microbiology:9943 talk.origins:312883 bionet.biophysics:3046

Rumple Stiltzski wrote:

> 

>      I am not a scientist myself, you so can gauge how much
> credibility you would like to lend my theory.
>      There is a form of light, as of yet undetected by human eye or
> aperatus, that dictates a large amount of survival instincts for life
> on our planets.  This 'colour' varies in 'hue, depth, degree' etc. and

You can't see it or detect it, but it exists. Trust me.

> depending on how certain parts of the brain respond, tell the
> biological creature what to do.  For example, there is a hue of
> undetected light that tells a bird to fly south; another that drives
> the lemmings over cliffs, and another that breaths life into potential
> life.
If you can't detect it, how does the brain respond to it?

>      This light, like all light, is an energy, and it sparks the gap
> between existance and non-existance much the way a sparkplug does in a
> Renault.

Ah ha! A Renault driver! Now we're getting somewhere.

>      The knowledge of this light is very muddled at the moment,

I would say muddled is an understatement. 

> the insinuations of it go by many different names.  Myself, I call it
> God for lack of better word.
Because you can't see, hear, touch, taste, or feel it or measure it with
any apparatus but you still think it exists despite any confirmatory
evidence. Good definition of God.

Andy the debunker

From owner-biophysics@net.bio.net Wed May 14 23:00:00 1997
Path: biosci!ihnp4.ucsd.edu!munnari.OZ.AU!news.ecn.uoknor.edu!feed1.news.erols.com!chippy.visi.com!news-out.visi.com!newsfeed.direct.ca!torn!kone!news.ccs.queensu.ca!not-for-mail
From: 4jch3@qlink.queensu.ca (Hesketh J Christian)
Newsgroups: bionet.biophysics
Subject: Ion Channel Web Page
Date: 14 May 1997 20:43:18 GMT
Organization: Queen's University, Kingston
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Message-ID: <5ld856$ro7@knot.queensu.ca>
NNTP-Posting-Host: qlink.queensu.ca
X-Newsreader: TIN [UNIX 1.3 950824BETA PL0]

The ion channel web page has recently been updated.  There is now a
developing ion channel forum, links to the home pages and a publication
list of several of the top ion channel researchers.  A complete human
voltage gated potassium channel sequence system has been installed as well
as other pertinent topics in current ion channel research.  Much work will
be going into this page over the next month, so check back often.  The URL
for this site is:

http://qlink.queensu.ca/~4jch3

Sincerely, 

---------------------------------------------------------------------------
J. Christian Hesketh
Queen's University - Kingston, Canada
Phone (613) 531-8048
e-mail: 4jch3@qlink.queensu.ca
Web Page (Research in Ion Channels): http://qlink.queensu.ca/~4jch3
      -Current research in ion channels with a biophysical perspective


From owner-biophysics@net.bio.net Fri May 16 23:00:00 1997
Path: biosci!bcm.tmc.edu!news.msfc.nasa.gov!europa.clark.net!news-peer.sprintlink.net!news.sprintlink.net!Sprint!howland.erols.net!newsfeed.internetmci.com!news.ycc.yale.edu!news
From: Richard Yu <ryu@laplace.csb.yale.edu>
Newsgroups: bionet.xtallography,bionet.biophysics
Subject: Protein crystal: Any suggestions for ATP heavy atom derivatives?
Date: Fri, 16 May 1997 22:40:56 -0400
Organization: Yale University
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Xref: biosci bionet.xtallography:3445 bionet.biophysics:3052

Greetings all:
	I'm wondering if any of you out there have ever used
a heavy metal derivatized ATP for an ATP binding protein,
or a funky derivative that happens to have an anomalously scattering
atom. I've got one reference on 2'-iodoATP, but can't seem to
find any others.

Thanks,
Rich

From owner-biophysics@net.bio.net Fri May 16 23:00:00 1997
Path: biosci!internet!biosci!not-for-mail
From: biohelp (BIOSCI Administrator)
Newsgroups: bionet.biophysics
Subject: BIOSCI/bionet miniFAQ & Fundraiser
Date: 17 May 1997 02:00:13 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 239
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <199705170900.CAA10695@net.bio.net>
NNTP-Posting-Host: net.bio.net

(LAST REVISION: 30-JUL-95)

This BIOSCI "miniFAQ" is designed to answer the questions that come up
the *most frequently*.  The main BIOSCI FAQ (Frequently Asked
Questions) is accessible on the World Wide Web at URL
http://www.bio.net/.

If you can not find an answer to your question in this or other
documentation, the BIOSCI technical support staff answers e-mail
queries sent to

		       biosci-help@net.bio.net

We can only answer questions about the use of the newsgroups and
mailing lists.  We unfortunately do not have the staff to do Internet
information searches or answer scientific questions.  Please post
those to the appropriate BIOSCI/bionet newsgroups.


	Contents:
	--------
	0) BIOSCI NEEDS YOUR SUPPORT!!

	1) Using the WWW to access the BIOSCI/bionet newsgroups.

	2) What to do about "spams," i.e., junk mail, ads, etc.

	3) Examples of subscribing and unsubscribing to the mailing lists.

	4) The BIOSCI user address and research interest directory.


0) BIOSCI NEEDS YOUR SUPPORT!!
------------------------------
BIOSCI's government funding has been expended, and we are now
operating solely from advertising revenue that we have raised from our
Web site at http://www.bio.net/.  We need just a few minutes of your
time to help us serve you.

You can do two important things which will take very little time for
you individually and will immensely help us continue to help you.

First, please use our WWW system at http://www.bio.net/ to access the
archives.  You can post or reply to messages via your Web browser as
described in item #1 below.  Your usage helps attract sponsors. If you
contact any of our sponsors, please be sure to thank them for
supporting BIOSCI. It is critical for them to get this feedback if
they are to continue their sponsorship for the long term.

Second, if you work for a company or organization that provides
products or services of interest to the biology community, please pass
this message on to your marketing or marketing communications
department or other appropriate group.  Please ask them to help
support BIOSCI by sponsoring our Web site and explain the uses and
benefits of the system to the biology community. If they are
interested, they can then contact us for further information at our
tech support address, biosci-help@net.bio.net.


1) Using the WWW to access the BIOSCI/bionet newsgroups.
--------------------------------------------------------
As of 10 December 1995, all BIOSCI/bionet full newsgroups are
accessible through the World Wide Web (WWW) at URL http://www.bio.net.
One can read and reply publicly or privately to both recent postings
and archived messages through one's Web browser if it is configured
properly to send e-mail.  Each newsgroup is equipped with its own WAIS
index.  The main BIOSCI home page also has access to the BIO-JOURNALS
Table of Contents database WAIS index and the BIOSCI user address
database described in another item further below.


2) What to do about "spams," i.e., junk mail, ads, etc.
-------------------------------------------------------
BIOSCI is a set of parallel USENET newsgroups (the "bionet" groups),
mailing lists, and a hypermail archive at URL http://www.bio.net/.
The same postings are distributed on all media (except for a small
number of mailing-list-only groups at net.bio.net).  Unfortunately it
is becoming a despicable practice on the Internet (by a few people out
to make a fast buck) to do automated mass postings to thousands of
newsgroups and mailing lists.  These attempts to grab free advertising
are refered to as "spams" in the usual, somewhat boneheaded, net
terminology.  USENET is more susceptible to this practice, and many
spams originate on the USENET groups and then are passed on to the
mailing lists.  However, spammers also get lists of mailing addresses
and hit these too, so neither medium is immune.

What should you do personally if you get junk mail?
---------------------------------------------------
Just delete it and move on without reading it further.  Filing a
protest is becoming increasingly useless because spammers are often
disguising the addresses where the messages are sent from.  Unless you
really understand Internet mail systems, your attempt at protest by
sending replies to the message will often end up being sent to the
address of an innocent person that the spammer is victimizing.

What can BIOSCI/bionet do to protect its newsgroups?
----------------------------------------------------
The only solution currently available is to moderate the newsgroup.
If this newsgroup is already moderated, then you are in good shape.
Moderation protects the USENET distribution from about 95% of the
spams that are being sent to date and protects the mailing lists
completely.  Moderation means, however, that someone has to take the
time to review each message before it goes out.  We have set up
software here that simply allows the moderator to forward to an
address at net.bio.net messages that (s)he wishes to have distributed.
This takes no more time than that needed to read the message and pass
it on, say about 1 min. per message.

Most newsgroups currently have a discussion leader who is responsible
for their newsgroup.  The discussions leaders and their e-mail
addresses are listed in the BIOSCI Information Sheet which is
available on the Web at http://www.bio.net/.  If a newsgroup is being
hit with too many junk postings, please contact the discussion leader
for that group and see if there is interest in moderating the group.
Please do not assume that by simply posting a complaint to the
newsgroup itself, anyone on the BIOSCI staff will act on your
complaint.  With close to 100 newsgroups to run, the BIOSCI staff has
to rely on the discussion leaders of each newsgroup to report problems
directly to us at biosci-help@net.bio.net.

We will moderate any of our newsgroups if the discussion leader tells
us that the readership of the group wishes to do so and if a moderator
is willing to do the work.  For most BIOSCI/bionet groups, this
entails only a few minutes of work each day.

Moderating a newsgroup will resolve probably 95% of the junk postings
on the USENET distribution.  Unfortunately there are easy ways for
determined spammers to override the moderation mechanism on USENET,
but we can protect our e-mail subscribers from unwanted postings if
the newsgroup is moderated.  You can also access our newsgroups over
the WWW at URL http://www.bio.net.  While this Web interface will not
stop spammers from trying to post to the groups, this will give you
yet another way, besides using USENET news, to keep the junk out of
your personal mail files.  For those of you with local USENET news
systems, the Web interface will also give you faster access to new
newsgroups and recent postings.


3) Examples of subscribing and unsubscribing to the mailing lists.
------------------------------------------------------------------
PLEASE NOTE: The BIOSCI management does NOT act on
subscription/unsubscription requests that are posted improperly to the
newsgroups and mailing lists.  People who do this only bother everyone
on the lists to no avail.  Please be sure to follow the proper
procedures below.

Gory details are in the BIOSCI Information sheets on the Web at
http://www.bio.net.  Below we give an example utilizing the
METHODS-AND-REAGENTS list at both of our two BIOSCI sites:

Users in the Americas and Pacific Rim countries who use the BIOSCI
------------------------------------------------------------------
node at computer net.bio.net:
----------------------------

A) Determine the "listname" which is the <=8 character mail address
                                         ^^^^^^^^^^^^^
   for the group.  These can be found in the BIOSCI Info. Sheet.  For
   the METHODS-AND-REAGENTS group the mailing address is
   methods@net.bio.net.  The listname is the portion of the address to
   the left of the @ sign, i.e., "methods".  The listname is used with
   the "subscribe" and "unsubscribe" commands illustrated below.

B) Mail all commands in the body of a mail message addressed to
   biosci-server@net.bio.net.  Do NOT send commands to the newsgroup
   posting addresses!  Leave the Subject: line blank, any text on it
   will be ignored.

C) In the body of your message put one or more of the following
   commands with an "end" command on the last line, e.g.,

   subscribe methods
   unsubscribe methods
   end

   Do NOT put your e-mail address or other text on these lines.  The
   server only allows you to cancel your subscription if the address
   on your mail header matches the address on our mailing list.
   Please ask for help at biosci-help@net.bio.net if your address has
   changed, e.g., if you know you are on the list but the server tells
   you that you are not a member.


Users in Europe, Africa, and Central Asia who use the BIOSCI node at
--------------------------------------------------------------------
computer daresbury.ac.uk (also known as dl.ac.uk):
-------------------------------------------------

To subscribe and unsubscribe to/from the BIOSCI lists, you need to
specify the full USENET newsgroup name with "bionet-news." prepended.
The USENET newsgroup names are listed in the BIOSCI Information sheet
on the Web at http://www.bio.net/.  For the METHODS-AND-REAGENTS list
the USENET newsgroup name is bionet.molbio.methds-reagnts, thus the
appropriate commands are

    sub bionet-news.bionet.molbio.methds-reagnts

    unsub bionet-news.bionet.molbio.methds-reagnts

These commands are included in a message addressed to mxt@dl.ac.uk,
NOT to the newsgroup mailing addresses.  As usual, include the text in
the body of the message as text on the Subject: line is ignored.

To unsubscribe from all the lists at the UK node, use

    unsub bionet-news

Please note that if the address in the list is different than the one
in your mail message header, you will not be able to unsubscribe by
this method. If you have problems, please mail biosci@daresbury.ac.uk.


4) The BIOSCI user address and research interest directory.
-----------------------------------------------------------
Please take this opportunity to add your name, address, and research
interest information to the BIOSCI User Address Database if you have
not already done so.

You can fill out the address form directly through our Web page at URL
http://www.bio.net/adrform.html.

The address database is reindexed nightly for WWW access (the URL is
http://www.bio.net/).  If you are not directly on the Internet but can
reach it by e-mail, please use our waismail server to access the user
directory.  waismail use is described above.  You can also request a
user address form by e-mail from biosci-help@net.bio.net.

Please check your database entry from time-to-time to see if your
address information is still up-to-date.  Because of our limited
personnel resources, we ask that you resubmit a *complete* form to
revise your entry; we only replace complete entries and do not have
resources to edit old forms.

				Sincerely,

				Dave Kristofferson
				BIOSCI/bionet Manager

				biosci-help@net.bio.net

From owner-biophysics@net.bio.net Sun May 18 23:00:00 1997
Newsgroups: bionet.biophysics
Path: biosci!daresbury!uninett.no!nntp.uio.no!newsfeeds.sol.net!europa.clark.net!cpk-news-hub1.bbnplanet.com!news.bbnplanet.com!EU.net!CERN.ch!news
From: "Chemical Dynamics" <gsl@tifrc3.tifr.res.in>
Subject: CURRICULUM-VITAE For Post-Doc in Biophysics
X-Nntp-Posting-Host: tifrc4.tifr.res.in
Message-ID: <01bc644c$9c1d76c0$0e1a909e@lakshmi.tifr.res.in>
Sender: news@news.cern.ch (USENET News System)
Organization: t i f r
X-Newsreader: Microsoft Internet News 4.70.1155
Date: Mon, 19 May 1997 12:13:08 GMT
Lines: 404

Name: Arvind Srivastava.
Institution: Tata Institute of Fundamental Research
E-Mail: asa225@tifrvax.tifr.res.in

Objective: To apply for Post-doc in the field of Biophysics
				


CURRICULUM-VITAE


Name:					Arvind Srivastava
Date  of birth:				13 August 1969
Institute:				Tata Institute of Fundamental Research
					Homi Bhabha Road 
					Bombay,  400 005, India.
Correspondence address:		Chemical Physics Group
					Tata Institute of Fundamental Research
					Homi Bhabha Road   
					Bombay, 400 005,  India 
Phone:					215 2971/215 2979 Ext. 2526.
Fax:					+ 91 - (22) - 215 2110
E-mail:				asa225@tifrvax.tifr.res.in

Educational qualifications

Degree/Exam.	           Year      	University			% Marks/Division 	
B. Sc.			1990	 Purvanchal University Jaunpur, U.P.	  67/1st Class	
M. Sc.(Chemistry)	1992	Banaras Hindu  University, Varanasi.	  68/1st Class	
Ph.D. (Chemistry)	1997	TIFR,  Bombay.			  Expected to complete 
									  by Sept. 1997.	

Graduate Course works

I have completed following courses as a part of my Ph.D. programme during
1992-1993.

Theoretical Courses

1.  Quantum Chemistry ; 2.  Molecular Biophysics ; 3.  Programming in C ; 
4.  Bio-Electrochemistry ; 5 . NMR Spectroscopy ;  6.  Bio-inorganic
Chemistry ; 
7.  Mathematical Methods ; 8.  Fluorescence Spectroscopy and Applications.

Experimental Projects

1	Production, Purification and Preliminary Characterization of Conserved 
    	region of "Myb" proteins; 
2	Elementary steps in proton transport across membranes; 
3	Rotational diffusion of Rose Bengal in various solvents.

Average grade in the above  courses was A-.



Ph.D. programme

After completing   graduate course work I joined  to Prof.
G.Krishnamoorthy, for my Ph.D. in January, 1994.  

 Ph.D.  Title:  Dynamics of Biological Systems.

Technical Experiences:

1.	I was involved in the installation of  a Time-resolved fluorescence
microscope which I have 	used  for  most of my experiments.
2.	I have used a CW mode-locked, frequency doubled Nd-YAG laser driven dye
(Rhodamine 6G 	and Pyridine 1) laser as the light source in all
mytime-resolved fluorescence and anisotropy 	studies. I have used
time-correlated single-photon-  counting set up as the detection system. I
	am familiar with the operation and maintenance of this system.
3.	All the data analysis were done using the program developed in
	C-language in our lab (by Prof. N. Periasamy).
4.	I  am familiar with cell culturing techniques.  
5.	I have practical and theoretical background in  other physical
techniques such as Steady-	State Fluorescence Spectroscopy (Shimadzu and
Flurolog 2), UV-VIS spectroscopy 	(Shimadzu UV-2100) and  Circular
Dichroism spectroscopy(Jasco-J600).

	Awards
	
1.	Junior Talent Search Scholarship. 
2.	National Scholarship
3.	Scholarship by the Tata Institute of Fundamental Research during
1992-1997.
4.	Financial award from Department of Science and Technology towards travel
to attend the XIIth 	International Biophysics Conference at Amsterdam, The
Netherlands, during 11th Aug.- 16th 	Aug. 1996.
5.	Financial support from Council of Scientific and Industrial Research
towards travel to attend 	the XIIth International Biophysics Conference at
Amsterdam, The Netherlands during 11th 	Aug.- 16th Aug. 1996.
6.	Best poster award by Indian Biophysical Society in 1996.
	
Talks given at various places:
	
1.	University of Pune, Feb. 1993 in SERC School on Chemical and Biological
Application of 	Laser.
2.	All India Institute of Medical Science, New Delhi on 21 Feb. 1996.
3.	Debye Institute, Department of  Molecular Biophysics, Buy Ballot
Laboratory,Utrecht 	University, Utrecht, The Netherlands, on 19th Aug.1996.
4.	Department of Chemistry, Celestijnenlaan 200F, Leuven,  Belgium on 20th
Aug. 1996.
5.	Inorganic Chemistry Division, Oxford University, UK on 22th Aug. 1996.
6.	Biochemistry  Department, Imperial College of Science, Technology and
Medicine, London, 	UK on 25th Aug. 1996.

 List of Publications

In Journals

1.	Arvind Srivastava and S. Doraiswamy, Rotational diffusion of Rose
Bengal, J. Chem. Phys. 	1995,  103, 6197.
2.	Anup Madan, P. K. Radha, Arvind Srivastava, Lakshmi C. Padhy and
Ramakrishna V. Hosur, 	The DNA-binding  domain of Drosophila melanogaster
c-Myb undergoes a ultistate 	denaturation. Eur. J. Biochem. 1995,  230,
733.
3.	Arvind Srivastava,  Shanteri Singh and G. Krishnamoorthy, Rapid
Transport of Protons across 	membranes by Aliphatic Amines and Acids, J.
Phys. Chem. 1995, 99, 11302.
4.	Arvind Srivastava and G. Krishnamoorthy, Time-Resolved Fluorescence
Microscopic 	Estimation of Cytoplasmic Viscosity, Progress in Biophys. &
Mol. Biol. 1996, 65, 192.
5.	 Madhavarao C. N. , Sauna Zuben E. ,Srivastava Arvind and Sitaram
V.,Voids Underlying 	Dynamics in Proteins Membranes and Micelles, Eur. J.
Biochem. 1997 (in press)
6.	 Arvind Srivastava and G. Krishnamoorthy, Cell Type  and Spatial
Location dependence of  	Cytoplasmic Viscosity Measured by Time-Resolved
Fluorescence Microscopy, Arch. Biophys. 	and Biochem. 1997, 340, 159-167.
7.	Arvind Srivastava and G. Krishnamoorthy, Time -Resolved Fluorescence
Microscopy Could 	Correct for Probe Binding While Estimating Intracellular
pH, Anal. Biochem. 1997, 249 (in 	press) 
8.	G. Krishnamoorthy and Arvind Srivastava, Intracellular Dynamics Seen
Through Time-	Resolved Fluorescence Microscopy, Current Science 1997,  (in
press)
9.	M. M. G. Krishna, Arvind Srivastava, Ranjan Das and N.
Periasamy,Translational and 	Rotational Dynamics of Surface Probes: Monte
Carlo Simulations and  Fluorescence 	Anisotropy Experiments. (Submitted)
	
In conferences

1.	Arvind Srivastava, Rotational Diffusion of Rose Bengal in Various
Solvents, SERC School on 	Chemical and Biological Application of Laser
Feb.1993.
2.	G. Krishnamoorthy, Ishak Ahmed, Shantheri Singh, Hari Pada Maity and
Arvind Srivastava, 	Rapid Transport of Protons across Membrane, Twelfth
School on Biophysics of Membrane 	Transport, School Proceedings, Poland,
May 4-13, 1994.
3.	Arvind Srivastava and G. Krishnamoorthy, Estimation of Cytoplasmic
Viscosity by Time-	Resolved Fluorescence Microscopy, XIIIth Indian
Biophysical Society meeting, All India 	Institute of Medical Science, New
Delhi, India, Feb. 1996.
4.	Arvind Srivastava and G. Krishnamoorthy, Time-Resolved Fluorescence
Microscopic 	Estimation of Cytoplasmic Viscosity, XIIth International
Biophysics Conference  at 	Amsterdam, The Netherlands, during 11th
Aug.-16th Aug. 1996
5.	Arvind Srivastava and G. Krishnamoorthy, Intracellular pH estimation by
Time-Resolved  	Fluorescence Microscopy, Symposium on Advances in
Bio-Inorganic Chemistry during 	October 7-12, 1996, Tata Institute of
Fundamental Research, Mumbai, India.
6.	Arvind Srivastava and G. Krishnamoorthy, Estimation of Intracellular pH
by Time -Resolved 	Fluorescence Microscopy, Indian Biophysical Society
meeting  during 9-12 Dec. 1996 at 	Indian Institute of Science,
Bangalore,India.
7.	G. Krishnamoorthy and Arvind Srivastava, Dynamic Fluorescence
Microscopic Observations 	on  Intracellular Mobility, during 9-12 Dec. 1996
at Indian Institute of Science, Bangalore, 	India.
8.	M. M. G. Krishna, Ranjan Das, Arvind Srivastava and N. Periasamy,
Translational and 	Rotational Dynamics of surface probes in Vesicles:
Computer simulational and  Fluorescence 	Microscopic experiments, during
9-12 Dec. 1996 at Indian Institute of Science, Bangalore, 	India.
9.	Krishnamoorthy and Arvind Srivastava, Cell Membrane Seen Through
Time-Resolved 	Fluorescence Microscopy, Thirteenth School on Biophysics of
Membrane Transport, School 	Proceedings, Poland, May 11-18, 1997.
	
	
Names & Addresses of  Referees

1.  Prof.  G. Krishnamoorthy
    Chemical Physics Group
    Tata Institute of Fundamental Research
    Homi Bhabha Road, Mumbai 400 005, India
    Fax: 091-22-215-2110
    E-mail: gk@tifrvax.tifr.res.in

2.  Prof.  N. Periasamy
    Chemical Physics Group
    Tata Institute of Fundamental Research
    Homi Bhabha Road, Mumbai 400 005, India
    Fax: 091-22-215-2110
    E-mail: peri@tifrvax.tifr.res.in

3.  Prof. S. Doraiswamy
    Chemical Physics Group
    Tata Institute of Fundamental Research
    Homi Bhabha Road, Mumbai 400 005, India
    Fax: 091-22-215-2110
    E-mail : edorai@tifrvax.tifr.res.in 

4.  Prof. R. V. Hosur
    Chemical Physics Group
    Tata Institute of Fundamental Research
    Homi Bhabha Road, Mumbai 400 005, India
    Fax: 091-22-215-2110
    E-mail: hosur@tifrvax.tifr.res.in

Research experiences

Instrumentation:

I was involved in the installation of a time-resolved fluorescence
microscope. This involved  coupling of a fluorescence microscope with
picosecond laser system. An inverted epifluorescence microscope (Nikon,
Diaphot 300) was optically modified in order to steer the dye laser pulses
into the optical path of the microscope. A CW mode-locked frequency-doubled
Nd-YAG laser-driven dye (Rhodamine 6G) laser which generates 4-10 ps pulses
was used .The laser beam  was vertically polarized and the polarization was
further restricted to   the vertical position by a polarizer placed at the
entrance  to the microscope. The laser beam was  guided to the objective
lens. The set - up is capable of  performing dynamic fluorescence
measurements on samples with a spatial resolution of 0.5-1.0 mm and a time
resolution of 50 ps. Also reliable data could be  obtained from even very
low levels (~102-103 molecules) of fluorophores.  The fluorescence which
was collected by  the same objective  lens was passed through cut-off
filters, a Glan-Taylor polarizer and a pin hole assembly (placed at the
image plane) and detected by a thermoelectrically cooled (Products for
Research, USA) fast response photomultiplier (XP2020Q). Time resolution of
the fluorescence signal was obtained by the time-correlated
single-photon-counting experimental setup. Spatial resolution of the sample
has been  achieved either by the focussed laser beam or by the pin-hole
kept at the image plane.


Experimental: 

Time-Resolved Fluorescence Microscopic Estimation of Cytoplasmic Viscosity

Information on the cell type and spatial location dependence of cytoplasmic
viscosity would be very useful in understanding some of the processes
occuring in the cell. For this purpose, the fluorescent dye Kiton Red
(sulforhodamine B) was  loaded into a variety of cells such as Swiss 3T3
fibroblast, human mononuclear cells, Sarcoma-180 tumor cell, Chinese
hamster ovary cells, the plant cells Digitalis Lanata , stamen hair cells
of Tradescantia  and guard mother cells of  Allium Cepa. Space-resolved
measurements of cytoplasmic viscosity were carried out by using an
experimental set-up wherein a picosecond laser system was coupled with an
epifluorescence microscope. Fluorescence lifetime measurements showed that
a large fraction ~70 % of Kiton Red was in the free form. Fluorescence
anisotropy decay of Kiton Red in cells was analyzed by a two population 
(free and bound) model. The microviscosity of cytoplasm was estimated from
the anisotropy decay kinetics of the free probe.  Correlation time of free
Kiton Red in cytoplasm  shows significant dependence on the cell type. The
following picture emerges from these data: (i) the cytoplasmic viscosity is
not very far from that of bulk water for all the cells studied;  (ii) the
average value of cytoplasmic viscosity is larger in  case of the  plant
cells when compared to those of the animal cells  studied here; (iii) the
positional variation in the value of cytoplasmic viscosity is larger in the
case of  the plant cells when compared to the animal cells and (iv)
cytoplasmic viscosity inside the tumor cell Sarcoma-180 is not different
from the normal mammalian cells studied here.  Model studies in various
simpler systems have shown that our  observation of cell type dependence 
and spatial location dependence  of the cytoplasmic viscosity could have
the origin in the variation in one or more of the following conditions
within the cells: (i) the level of structured water, (ii) the concentration
of small and macromolecules, (iii) the hydrodynamic shape (compact or
extended structure) of  the molecules present and (iv) physical
restrictions such as proximity of membrane,  cytoskeletal network etc.

Estimation of Intracellular pH  by Time-Resolved Fluorescence Microscopy

Optical measurement of intracellular pH measurement scores over other
methods of  pH measurements in the respect of facile measurement of real
time variation of intracellular pH  and the capability to map the spatial
variation of pH within a single cell with the help of a fluorescence
microscope. Although fluorescence intensity is the most convenient
parameter for measurements, the convenience is offset by various
uncertainties in the estimation of pH. Apart from the pH, the fluorescence
intensity would also depend upon  factors such as concentration of the
probe, pathlength of the observation, light scattering , photobleaching 
and binding of the probe to macromolecules and membranes. Estimation of pH
using fluorescence lifetime would eliminate the above mentioned drawbacks.
We have used the fluorescent pH indicator SNARF-1 in estimating the
intracellular pH in a variety of cells. A fluorescence microscope coupled
with a picosecond laser system was used in these measurements. The
principle of lifetime-based pH sensing lies in the estimation of the
relative amplitudes of the lifetime components of the protonated and
deprotonated forms of the probe which have distinctly different lifetimes.
The main advantage of lifetime based sensing is the absence of complication
due to changes in the pathlength of the observation, concentration of the
probe, absence of  light scattering and photobleaching. Also probe binding
to the macromolecules and membranes could be taken into account while
analyzing fluorescence decay curve. Our analysis show  that probe binding
could result in significant errors in pH-estimations based on steady-state
intensity measurements such as the popular ratiometric methods.
The origin of this difference lies in the higher value (~3 ns) of the
lifetime of the  predominant population of bound probe when compared to
those of  the free forms.   In case where a fourth lifetime component ( ~
0.1 ns) was observed, the pH value estimated by steady state was lower than
that estimated by the renormalized amplitude. 

Study of Membrane Fluidity by Fluorescence Lifetime Distribution:

The physical state of cell membranes is relevant in many functions of the
cell and hence a knowledge on them is important for a complete description
of cell physiology. In the past a variety of physical techniques have been
employed for this purpose. In the present work we show the usefulness of
lifetime distribution of the membrane probe Nile Red in obtaining
information on the physical state of membranes. We have used the
time-resolved fluorescence microscopic technique  Liposomal membranes,
planar supported membranes and membranes of various intact cells were
probed under a variety of conditions. Fluorescence decay curves were
analyzed by the Maximum Entropy Method (MEM) to obtain distribution of
fluorescence lifetime of Nile Red in membranes.  The width of lifetime
distribution  was used to characterize the heterogeneity of the membrane.
In model systems such as DPPC and DMPC membranes, the width associated with
MEM lifetime distributions of Nile Red was very sensitive to the physical
state of the membrane. The width in the gel state was higher when compared
to that in liquid crystalline state by about 5 fold. Temperature dependence
of the width  tracked exactly the physical state of lipid. The width was
also sensitive to membrane composition such as the presence of cholesterol,
membrane proteins and fatty acids.   The following conclusions emerged from
 these data: (i) The width observed in  the mammalian cells studied here
were significantly larger when  compared to those observed in the plant
cells; (ii) the variation in the width observed in a single mammalian cell
was about 2-3 fold which is significantly larger than the variation
observed in the plant cells and (iii) the width observed in plasma
membranes were larger when compared to the nuclear membrane in the
mammalian cells. The last observation could be due to the fact that plasma
membranes have higher level of cholesterol when compared to nuclear
membranes 

Rapid Transport of Protons across membranes by Aliphatic acids and Amines

The pH gradient generated across membranes can be dissipated efficiently by
means of single turnover cycle of aliphatic amines and acids present in the
membrane. The kinetics of this process was in the submillisecond timescale
and was measured by creating pH gradients using temperature jump. The main
principal behind this technique is the difference in the enthalpy changes
associated with protonation equilibria of various pH buffers. Application
of T- jump to a vesicular suspension having, for example  Tris in the
external  aqueous phase and phosphate in the inner aqueous phase produces a
DpH within  ~2 ms. The decay of DpH (transmembrane proton transport)  was
measured fluorimetrically by the use of the fluorescent indicator Pyranine
entrapped inside the vesicles. The observed DpH decay process was
identified as due to  rapid transmembrane movement of the neutral form of
either the acid or the amine. The rate constant was estimated to be in the
range of 1-6 x 103 s-1 in the case of aliphatic amines.

Correlation of proton transport with water content of membranes

Transmemembrane  proton transport was measured in various lipid vesicles in
order to correlate proton permeability coefficient  with the hydration  of
the acyl chain. We have used the vesicles made up of  pure saturated lipids
DMPC, Egg PC, DPPC mixed lipid  Soybean phospholipid and variety of
unsaturated lipids like  C14:1, C16:1, C18:1 , C20:1, C22:1 PC.   The
transmembrane permeability  of proton was measured by giving a pH jump and
monitoring the rate of change of internal pH with the help of fluorescent
pH indicator pyranine trapped inside.  The level of hydration of the acyl
chain was estimated by measuring the fluores