From owner-biophysics@net.bio.net Fri Oct 01 03:07:00 1999
Path: biosci!CLUST.CH.CAM.AC.UK!zoizeage49
From: zoizeage49@CLUST.CH.CAM.AC.UK (usyeris)
Newsgroups: bionet.biophysics
Subject: --Free--Weight.Loss.Gift
Date: 30 Sep 1999 21:07:34 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 25
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <199909304109KAA51909@seodik.robotron.de>
NNTP-Posting-Host: net.bio.net


Greetings from Physician's Weight Management,

My name is Dr. Hinman.  I am a physician and weight loss 
specialist.  My studied base of 1500 patients has consistently 
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Many dieting patients have experienced results ranging from 1/2 to 
1 lb. per day of body fat loss.  Dieting patients should not be 
surprised to experience weight loss of up to 15 to 30 lbs. during the 
first thirty days.  These results vary by patient, but significant 
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demonstrated NO significant side effects, is all natural and is easy 
to use.    

Please reply by e-mail for further information and you will receive
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obligation.

Send an email to bord34@bigfoot.com  with the subject "diet"

To be deleted from our list, just email bord34@bigfoot.com
with the subject line as 'delete' and we shall delete your address.
        
*-*-Loosin lbs..

From owner-biophysics@net.bio.net Fri Oct 01 15:10:00 1999
Path: biosci!aecom.yu.edu!mrc
From: mrc@aecom.yu.edu ("Dr. Mark Chance")
Newsgroups: bionet.biophysics
Subject: Research Scientist Position
Date: 1 Oct 1999 09:10:30 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 38
Sender: daemon@net.bio.net
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Message-ID: <1.5.4.32.19991001160110.00a50c54@medusa.bioc.aecom.yu.edu>
NNTP-Posting-Host: net.bio.net

Research position in molecular biology available at Brookhaven
laboratories and Center for Synchrotron Biosciences (see URL below). 
The successful candidate will have experience in P-32
labeling and handling of labeled nucleic acids (experience with RNA
in particular is a plus), running of sequencing gels, and have
related biochemistry experience. Familiarity with instrumentation
and computer analysis related to gel imaging is desirable.
Alternatively, experience with stopped flow or synchrotron beamlines
is also desirable. Positions are available for both B.S. and Ph.D. scientists. 
Salary commensurate with experience.

For further information, please contact Mark Chance at
mrc@aecom.yu.edu or fax a letter and cv to the address below

-------------------------------------------------------------
Mark R. Chance, Albert Einstein College of Medicine
Center for Synchrotron Biosciences, An NIH Shared Resource
Ullman 315, Department of Physiology & Biophysics
1300 Morris Park Ave., Bronx NY 10461
ph. 718-430-4136; fax-718-430-8587; internet : mrc@aecom.yu.edu
http://beam.aecom.yu.edu/Phys&bio/csb1.htm

*********************************************
Mark R. Chance,  Professor of Physiology & Biophysics and Biochemistry 
and Director, Albert Einstein Center for 
Synchrotron Biosciences, An NIH Resource Center
Albert Einstein College of Medicine
Ullmann 315, Department of Physiology & Biophysics
1300 Morris Park Ave., Bronx NY 10461
ph. 718-430-4136; fax-718-430-8587; internet : mrc@aecom.yu.edu
http://beam.aecom.yu.edu/Phys&bio/csb1.htm
Also
National Synchrotron Light Source, Brookhaven National Labs
Building 725A-X9
Upton NY 11973
ph: 516-344-3800; fax-516-344-5594
*********************************************


From owner-biophysics@net.bio.net Fri Oct 01 20:59:00 1999
Path: biosci!candseek.com!915613
From: 915613@candseek.com
Newsgroups: bionet.biophysics
Subject: JOBOP Scientist
Date: 1 Oct 1999 14:59:57 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 72
Sender: daemon@net.bio.net
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Message-ID: <199910012159.OAA04332@net.bio.net>
NNTP-Posting-Host: net.bio.net


Since your email address was listed on a related web site 
page or database, I thought you might help. I am seeking 
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A Ph.D. scientist to work in a lab that is responsible for the 
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research facilities in Westchester, New York and can provide 
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Geographic Location of Position: US-NY

If you know anyone that might be interested, please forward 
this to them or contact:

Billy Gathers
Diedre Moire Corporation 
Fax: 609-584-9575
Voice 609-584-8733 Ext. 235
Email: 915613@candseek.com

To permanently discontinue receiving employment 
opportunity notices from any and all help wanted 
advertisers using the Candidate Seeker system, 
click your "Reply" button and type the word "re-
move" without spaces between the letters 
into the SUBJECT field then click the "Send" 
button. Your email address will be permanently 
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Please feel free to contact the candidateseeker.com 
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number for job related questions. All job related 
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replying to contact addresses or phone numbers 
indicated at the end of the job description message.



Mailed By:

candseek.com
510 Horizon Center
Robbinsville, NJ 08691


From owner-biophysics@net.bio.net Sat Oct 02 07:38:00 1999
Path: biosci!263.NET!howie_wang
From: howie_wang@263.NET ("Hong Wang")
Newsgroups: bionet.biophysics
Subject: subscribe
Date: 2 Oct 1999 01:38:22 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
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From owner-biophysics@net.bio.net Sat Oct 02 11:15:00 1999
Path: biosci!BESTWAY.COM.BR!juliu85
From: juliu85@BESTWAY.COM.BR (loskiee)
Newsgroups: bionet.biophysics
Subject: Adv : make your computer fully y2k compliant
Date: 2 Oct 1999 05:15:16 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 55
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <199910021512OAA50188@yuisuwe.fsa.is>
NNTP-Posting-Host: net.bio.net

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From owner-biophysics@net.bio.net Sat Oct 02 23:28:00 1999
Path: biosci!PRISTINE.COM.TW!mortgage2000
From: mortgage2000@PRISTINE.COM.TW
Newsgroups: bionet.biophysics
Subject: Home loans even if you have bad credit!
Date: 2 Oct 1999 17:28:32 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 65
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <199910030030.CAA05515@morena.ing.uni.wroc.pl>
Reply-To: hcheldon@iobox.com
NNTP-Posting-Host: net.bio.net

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-------------------------------------------------
This email complies with ALL Federal and State laws.

To be removed from the mailing list send 
mailto:HCheldon@iobox.com?subject=remove_tc3


















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From owner-biophysics@net.bio.net Sun Oct 03 01:27:00 1999
Path: biosci!MINDSPRING.COM!mowhc
From: mowhc@MINDSPRING.COM
Newsgroups: bionet.biophysics
Subject: Homeworkers Needed!
Date: 2 Oct 1999 19:27:16 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 147
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <733.136224.836746@ns.bigbear.net>
NNTP-Posting-Host: net.bio.net

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Name_____________________________________________________

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From owner-biophysics@net.bio.net Mon Oct 04 02:33:00 1999
Path: biosci!rutgers!gatech!howland.erols.net!peer.news.verio.net.MISMATCH!iad-peer.news.verio.net!news.verio.net!ord-feed.news.verio.net!feed.news.verio.net!cletus.bright.net!none444.yet
From: no.email.address.entered@none444.yet
Newsgroups: bionet.biophysics
Subject: FREE LEAN CHILI RECIPES_ FREE!!!
Message-ID: <03109923.2105@none444.yet>
Organization: <no organization>
Reply-To: qms.bright.net
Lines: 1
Date: Sunday, 03 Oct 1999 23:21:05 -0600
NNTP-Posting-Host: 209.143.35.181
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X-Trace: cletus.bright.net 939007505 209.143.35.181 (Sun, 03 Oct 1999 23:25:05 EDT)
NNTP-Posting-Date: Sun, 03 Oct 1999 23:25:05 EDT

FREE RECIPES AT qms@bright.net . Put food as subject!!

From owner-biophysics@net.bio.net Tue Oct 05 09:18:00 1999
Path: biosci!pravda.ucr.edu!ihnp4.ucsd.edu!gondor!newshub.sdsu.edu!newsfeed.berkeley.edu!diablo.theplanet.net!news.theplanet.net!newspost.theplanet.net!not-for-mail
From: "Clive Delmonte" <clivedelmonte@c-i-delmonte.freeserve.co.uk>
Newsgroups: bionet.biophysics
Subject: DNA Structure Puzzle Number 1
Date: Tue, 5 Oct 1999 11:11:49 +0100
Organization: Customer of Planet Online
Lines: 42
Message-ID: <7tcirn$h7a$1@news4.svr.pol.co.uk>
NNTP-Posting-Host: modem-6.vanadium.dialup.pol.co.uk
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PUZZLE NUMBER 1

Microprobe Studies of DNA Give New Insights into Duplex Structure

In their STM study of nucleic acids (1), Lee et al. recorded in their Figure
3(b) lengthy stretches of at least four well-resolved linear DNA duplexes.

The vital feature of this very clear image of DNA molecules is that no
plectonaemic winding can be discerned. That is, they show no sign of being
double-helical. The duplexes consist of long, paired, helices with a
consistent, uninterrupted contour running between the two strands of each of
the four duplexes, whose highlighted features remain exactly in phase with
each other over their whole lengths, extending to some 17 - 20 full helical
turns.

In their Figure 3(d) is shown the height of the duplex, that is, its
diameter as it lies on the substrate, equal to some 1.3nm. Their images
fully accord with the sketch of B-DNA set out in the website, and shown in
Ref. 2 (page 48), for which the cross sectional, helical dimensions are
determined solely by the width of the Watson-Crick base pair, namely 1.1 nm,
connected across the helices, while the pitch remains at 3.34nm.

In Ref. 2 (pages 51, 149, 170) there are details of three independent
demonstrations reported by different researchers, deducible from
experimental work in the literature, that Isomer 2 (defined in the website)
is that which is actually found in DNA in vivo, and that Isomer 1 is
unknown.
-------------------------------------------------------------
1 Scanning Tunnelling Microscopy of Nucleic Acids; G. Lee, P.G. Arscott,
V.A. Bloomfield & D. Fennell Evans; SCIENCE Vol 244 (1989) 475 - 477
2 Towards A New Structural Molecular Biology, by Clive Delmonte, ISBN 0
9512276 0 2 (1991)


Clive Delmonte

For a view of all the DNA Structure Puzzles
and the DNA publications, please refer to:
http://www.c-i-delmonte.freeserve.co.uk



From owner-biophysics@net.bio.net Wed Oct 06 03:52:00 1999
Path: biosci!CHEF.NET!snoopy34
From: snoopy34@CHEF.NET
Newsgroups: bionet.biophysics
Subject: Message From Juliana
Date: 5 Oct 1999 21:52:09 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 57
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <7727DABBEEC.ABK5BB@mail.asae.com.mx>
NNTP-Posting-Host: net.bio.net

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From owner-biophysics@net.bio.net Wed Oct 06 11:51:00 1999
Path: biosci!newshost.lanl.gov!logbridge.uoregon.edu!news.maxwell.syr.edu!news.idt.net!nntp.farm.idt.net!news
From: "NDRI/HBDI" <hbdi@idt.net>
Newsgroups: alt.bio.technology,alt.bio.technology.misc,bionet,bionet.biology,bionet.biophysics,bionet.cellbiol
Subject: Autopsy, Surgical Discard and Transplantation Tissues for Now Available for Research
Date: Wed, 6 Oct 1999 08:41:27 -0400
Organization: IDT (Best News In The World)
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Xref: biosci bionet.biophysics:5255 bionet.cellbiol:12612

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From owner-biophysics@net.bio.net Wed Oct 06 15:06:00 1999
Path: biosci!BOOM.COM!dvds
From: dvds@BOOM.COM
Newsgroups: bionet.biophysics
Subject: *DVD Player Blowout - Only $179!!
Date: 6 Oct 1999 09:06:00 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 56
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <199910061517.LAA17297@ing.udec.cl>
NNTP-Posting-Host: net.bio.net

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From owner-biophysics@net.bio.net Thu Oct 07 02:01:00 1999
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From: madQ <madq968@djeksta.comNOSPAM>
Newsgroups: bionet.biophysics
Subject: Download Ia.n.i.!!! It's free!
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From owner-biophysics@net.bio.net Thu Oct 07 13:25:00 1999
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From: "Novartis Italia" <tetyzac@tin.it>
Newsgroups: bionet.biophysics
Subject: Parliamo di biotech
Date: Thu, 7 Oct 1999 15:40:56 +0200
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Parliamo di biotech con gli esperti

Giorgio Poli e Francesco Sala, due docenti universitari, rispondono alle
domande del pubblico, per chiarire dubbi e approfondire i diversi temi
relativi alle biotecnologie

Origgio, 7 ottobre 1999 – Da oggi è attivo un nuovo servizio per tutti gli
utenti Internet che volessero approfondire i temi delle biotecnologie. Si
tratta di ‘Parliamo di biotech’, un forum condotto da due docenti
universitari milanesi: Giorgio Poli (docente di Microbiologia e Immunologia
veterinaria) e da Francesco Sala (docente di Botanica e Biotecnologie
Vegetali), che si avvarranno anche del contributo di altri esperti. Il
servizio è stato realizzato in collaborazione con Novartis ed è disponibile
all’indirizzo: www.it.novartis.com

Il forum nasce dal desiderio di offrire al pubblico un ambito nel quale
dialogare con gli esperti, su temi che hanno riscosso grande attenzione e
suscitato numerosi quesiti. Poli e Sala risponderanno alle domande degli
utenti Internet, che potranno proporre anche proprie riflessioni e commenti.

L’intento è quello di approfondire gli argomenti principali relativi alle
biotecnologie, che saranno affrontati con un linguaggio divulgativo,
rispettando l’indispensabile rigore scientifico.



Per ulteriori informazioni:
Terry Tyzack
Novartis Italia Comunicazione
Tel. 02/96543260 – fax 02/96701090
e-mail: terry.tyzack@group.novartis.com





From owner-biophysics@net.bio.net Thu Oct 07 19:40:00 1999
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Subject: Download Ia.n.i.!!! It's free!
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From owner-biophysics@net.bio.net Sun Oct 10 10:40:00 1999
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From: "Clive Delmonte" <clivedelmonte@c-i-delmonte.freeserve.co.uk>
Newsgroups: bionet.biophysics,bionet.xtallography
Subject: DNA STRUCTURE PUZZLE NUMBER 2
Date: Sun, 10 Oct 1999 12:27:19 +0100
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Xref: biosci bionet.biophysics:5263 bionet.xtallography:4945

DNA STRUCTURE PUZZLE NUMBER 2

Optical Diffraction Compared With X-Ray Diffraction for B-DNA

It was Franklin's famous diffraction photograph of B-DNA (3), set out in the
website, shown to him by Wilkins, that Watson sketched on the train back to
Cambridge to rejoin Crick.

One of Wilkins' collaborators, A R Stokes (4), produced probably the first
optical diffraction prediction of the pattern arising from a true
side-by-side helical structure, set out in the website, this one having 8
repeat units per full turn. This true side-by-side structure mirrors that
found in Ref. 1(Puzzle #1)) by STM.

Stokes' optical diffraction pattern would seem to resemble closely
Franklin's X-ray diffraction pattern of B-DNA.

In the same paper (4), Stokes, from his work on the Fourier transform for a
helix, showed that, defining as "delta" the angle between an arm of the
"helical cross" and the Y-axis (meridian):

tan delta = helical pitch / helical circumference

Applying this result to Franklin's photograph of B-DNA, delta is measured as
40 degrees, and, with a pitch of 3.34 nm, the helical diameter is found to
be some 1.3 nm.  It seems that Stokes' result was never applied to B-DNA
diffraction photographs by Crick, Watson, Wilkins, Franklin or Stokes.

Even in later work with better definition, for example, from Wilkins' group
on Li-DNA, included in the website, we see a similar value of delta.

For a supposed double helical diameter of 2 to 2.2 nm, delta should be 28 -
26 degrees respectively, far removed from the actual values of 40 - 41.

The helical diameter of 1.3 nm, found from Stokes' equation applied to
Franklin's & Wilkins' photographs, coincides with the STM value of 1.3 nm
measured by Lee et al. (Puzzle #1, Ref. 1), recorded in their Figure 3d, and
accords with the Watson-Crick base pair width of 1.1 nm which itself
determines the sugar-phosphate chain diameter set out in Ref. 2.
----------------------------------------------
3 Molecular Configuration in Sodium Thymonucleate; R.E. Franklin &
R.G.Gosling; Nature Vol 171 (1953) 740-741
4 The Theory of X-ray Fibre Diagrams; A.R. Stokes; Prog. Biophys. & Biophys.
Chem. Vol 5 (1955) 140-167
---------------------------------------------
Clive Delmonte

For a view of all the DNA Structure Puzzles
and the DNA publications, please refer to:
http://www.c-i-delmonte.freeserve.co.uk



From owner-biophysics@net.bio.net Sun Oct 10 19:27:00 1999
Path: biosci!rutgers!gatech!purdue!yuma!usenet
From: "Ryan D. Alexander" <ryanalex@lamar.colostate.edu>
Newsgroups: comp.lang.fortran,bionet.molec-model,comp.programming,sci.math,sci.stat.math,bionet.biophysics
Subject: Monte Carlo Minimization Routine ???
Date: Sun, 10 Oct 1999 14:09:29 -0600
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In attempting to model chromosomes packed within a nucleus, I've decided that I
need a type of Monte Carlo Minimization routine.  Scouring the Web has turned up
little in the way progress, so I've turned to you all in NG-Land...

Essentially I'm looking for an algorithm (in Fortran 77/90, preferably) where I
may enter a set of initial cartesian coordinates, the associated radii for each
"chromosome," and an objective function (i.e. Lennard-Jones potential
function).  Let the program calculate the value of my objective function, Monte
Carlo (smartly) to re-position the chromosomes, recalculate the potential, etc.,
etc. until the function value is minimized.

Anyone's help (books, articles, URL's) would be greatly appreciated!!  If anyone
in the realm of molecular dynamics, or packing theory (of non-uniform shapes)
have any ideas, I'd obviously welcome them as well.

Thanks in advance... (oh & as this is probably not of general interest to these
ng's please just e-mail me directly if you'd like)
-- Ryan D. Alexander
=========================================================
Ryan D. Alexander, CSU-LBNL NSCORT Ph.D. Trainee
Colorado State Univ., Dept. of Radiological Health Sciences
E-mail: ryanalex@lamar.colostate.edu
Office Ph: 970-491-0520, Dept. Fax: 970-491-0623
=========================================================



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From owner-biophysics@net.bio.net Mon Oct 11 03:05:00 1999
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From: madQ <madq968@djeksta.comNOSPAM>
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Subject: Download Ia.n.i.!!! It's free!
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From owner-biophysics@net.bio.net Mon Oct 11 03:06:00 1999
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From owner-biophysics@net.bio.net Mon Oct 11 08:32:00 1999
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From: Boudeville Yves <boudevil@catalyse.univ-lyon1.fr>
Newsgroups: comp.lang.fortran,bionet.molec-model,comp.programming,sci.math,sci.stat.math,bionet.biophysics
Subject: Re: Monte Carlo Minimization Routine ???
Date: Mon, 11 Oct 1999 11:24:19 -0700
Organization: CNRS
Message-ID: <38022B53.6418@catalyse.univ-lyon1.fr>
References: <3800F279.AD543BD3@lamar.colostate.edu>
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Xref: biosci bionet.molec-model:2751 bionet.biophysics:5268

Ryan D. Alexander wrote:
> 
 Monte-Carlo methods and simulated annealing are good for monomodal
mathematical functions. But is it really the case in MM ? Two ways :
One random based "the genetic algoritms", David E; Goldberg, Addison
Wesley can be benefit because you have not only the "minimum minimorum"
but also the "local minima" of a multimodal function. The most robust
way, a little less expensive, can be the flexible simplex methods
(from G.E.P. Box ? if my memory is right).
Friendly. Yves.
> In attempting to model chromosomes packed within a nucleus, I've decided that I
> need a type of Monte Carlo Minimization routine.  Scouring the Web has turned up
> little in the way progress, so I've turned to you all in NG-Land...
> 
> Essentially I'm looking for an algorithm (in Fortran 77/90, preferably) where I
> may enter a set of initial cartesian coordinates, the associated radii for each
> "chromosome," and an objective function (i.e. Lennard-Jones potential
> function).  Let the program calculate the value of my objective function, Monte
> Carlo (smartly) to re-position the chromosomes, recalculate the potential, etc.,
> etc. until the function value is minimized.
> 
> Anyone's help (books, articles, URL's) would be greatly appreciated!!  If anyone
> in the realm of molecular dynamics, or packing theory (of non-uniform shapes)
> have any ideas, I'd obviously welcome them as well.
> 
> Thanks in advance... (oh & as this is probably not of general interest to these
> ng's please just e-mail me directly if you'd like)
> -- Ryan D. Alexander
> =========================================================
> Ryan D. Alexander, CSU-LBNL NSCORT Ph.D. Trainee
> Colorado State Univ., Dept. of Radiological Health Sciences
> E-mail: ryanalex@lamar.colostate.edu
> Office Ph: 970-491-0520, Dept. Fax: 970-491-0623
> =========================================================

-- 
-------------------------------------------------
I Dr. Yves Boudeville; Theory Group / ENS-Lyon, I
I Institut de Recherches sur la Catalyse, CNRS  I
I 2, Avenue Albert EINSTEIN ;                   I
I F69626 VILLEURBANNE Cedex ; FRANCE .          I
I Ph: (+33.4.72...or) 04.72.44.53.49 (in France)I
I Fax:(+33.4.72...or) 04.72.44.53.99 (in France)I
I E-mail: boudevil@catalyse.univ-lyon1.fr       I
I http://www.ens-lyon.fr/~boudevil/             I
-------------------------------------------------

From owner-biophysics@net.bio.net Mon Oct 11 10:47:00 1999
Path: biosci!cc.UManitoba.CA!gordonr
From: gordonr@cc.UManitoba.CA (Richard Gordon)
Newsgroups: bionet.biophysics
Subject: Monte Carlo Minimization Routine ???/In Vivo
Date: 11 Oct 1999 04:46:31 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 119
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Dear Ryan,
In Vivo, which is under development, should meet your requirements. See
abstract below.
Yours, -Dick

In Vivo: A Cytoskeleton Simulator
for Problems in Cell and Developmental Biology

Randy J. Zauhar
Dept. Chemistry & Biochemistry, University of the Sciences Philadelphia
600 S. 43rd Street
Philadelphia PA 19104-4495, USA
Phone: (215) 596-8691, Fax: (215) 596-8543
E-mail: r.zauhar@usip.edu

Edmond Abrahamian
Tripos, Inc.
1699 S. Hanley Road, Suite 303
St. Louis MO 63144, USA
Phone: (800) 323-2960, Fax: (314) 647-9241
E-mail: edmond@greencedars.com

Richard Gordon
Departments of Radiology and Electrical & Computer Engineering
University of Manitoba, Health Sciences Centre
820 Sherbrook Street, Winnipeg, MB R3A 1R9 Canada
Phone: (204) 789-3828,  Fax: (204) 787-2080
E-mail: GordonR@cc.UManitoba.ca
Vice-President, Canadian Association for Responsible Research Funding

J. Theor. Biol., Joel Keizer Memorial special issue, in preparation.

Abstract: Since the first days of electronic computing, there has been a
strong focus on the development of techniques for atomic scale simulation
of a wide variety of molecular systems, from liquids to macromolecules and
everything in between. These methods have ranged in physical detail from
those that include details of electronic structure to those which model
much of the system of interest as a continuum, and thus exclude even some
atomic details.

At present, methods based on molecular mechanics can model systems that
comprise up to several million atoms. These simulations typically involve
applications to complexes of several large biomolecules, or to the modeling
of material properties. While simulations of these sizes hold great promise
for elucidating atomic level behavior for many interesting systems, they
are inadequate for the application we consider here: that is, the
simulation of significant pieces of cytoskeletal machinery. These include
the various networks of actin, myosin and associated proteins that are
involved in structural support of the cell, in locomotion, and in
development, and microtubule structures such as the mitotic apparatus.

Between methods such as Virtual Cell, which model aspects of physiology at
a high level in three dimensions, and atom-level simulations of proteins,
there is a "twilight zone" that is largely unoccupied. This middle ground
includes those methods aimed at simulating very large polymerized systems
such microfilaments, intermediate filaments, and microtubules. Here we
review the methodologies that currently exist, and discuss the systems they
have been applied to. We describe the design of In Vivo, a computer
application we are currently developing that is intended as a general
simulator of very large cytoskeletal components.

We envisage a number of applications for In Vivo, such as the dynamics of
intracellular trafficking, simulation of the spindle apparatus, and
cellular motility. The program is intended to allow side by side comparison
of simulations with time lapse movies, with interactive alteration of
parameters to attempt a match. Our particular interests are in the realm of
nonlinearities in cellular tensegrity structures, such as the operation of
the cell state splitter in embryo cell differentiation, and the role of the
cortex in symmetric versus asymmetric cell division. In Vivo could also be
used for testing models of the 3D structure of chromosomes and their
changes during altered gene expression.

>To: biophys@net.bio.net
>From: "Ryan D. Alexander" <ryanalex@lamar.colostate.edu>
>Subject: Monte Carlo Minimization Routine ???
>Date: Sun, 10 Oct 1999 14:09:29 -0600
>NNTP-Posting-Host: mc5126.cvmbs.colostate.edu
>Mime-Version: 1.0
>X-Accept-Language: en
>
>In attempting to model chromosomes packed within a nucleus, I've decided
>that I
>need a type of Monte Carlo Minimization routine.  Scouring the Web has
>turned up
>little in the way progress, so I've turned to you all in NG-Land...
>
>Essentially I'm looking for an algorithm (in Fortran 77/90, preferably)
>where I
>may enter a set of initial cartesian coordinates, the associated radii for
>each
>"chromosome," and an objective function (i.e. Lennard-Jones potential
>function).  Let the program calculate the value of my objective function,
>Monte
>Carlo (smartly) to re-position the chromosomes, recalculate the potential,
>etc.,
>etc. until the function value is minimized.
>
>Anyone's help (books, articles, URL's) would be greatly appreciated!!  If
>anyone
>in the realm of molecular dynamics, or packing theory (of non-uniform shapes)
>have any ideas, I'd obviously welcome them as well.
>
>Thanks in advance... (oh & as this is probably not of general interest to
>these
>ng's please just e-mail me directly if you'd like)
>-- Ryan D. Alexander
>=========================================================
>Ryan D. Alexander, CSU-LBNL NSCORT Ph.D. Trainee
>Colorado State Univ., Dept. of Radiological Health Sciences
>E-mail: ryanalex@lamar.colostate.edu
>Office Ph: 970-491-0520, Dept. Fax: 970-491-0623
>=========================================================

Dr. Richard Gordon, Radiology, U. Manitoba, HSC, 820 Sherbrook Street,
Winnipeg R3A 1R9 Canada, Phone: (204) 789-3828, fax: (204) 787-2080/ Book
just out: The Hierarchical Genome & Differentiation Waves: Novel
Unification of Development, Genetics & Evolution:
http://www.wspc.com.sg/books/lifesci/2755.html, E-mail:
GordonR@cc.UManitoba.ca

From owner-biophysics@net.bio.net Mon Oct 11 12:34:00 1999
From: "David Jones" <dajxxx@mail.nwl.ac.uk>
Newsgroups: comp.lang.fortran,bionet.molec-model,comp.programming,sci.math,sci.stat.math,bionet.biophysics
References: <3800F279.AD543BD3@lamar.colostate.edu>
Subject: Re: Monte Carlo Minimization Routine ???
Date: Mon, 11 Oct 1999 12:29:41 +0100
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Xref: biosci bionet.molec-model:2752 bionet.biophysics:5270


Ryan D. Alexander <ryanalex@lamar.colostate.edu> wrote in message
news:3800F279.AD543BD3@lamar.colostate.edu...
> In attempting to model chromosomes packed within a nucleus, I've decided
that I
> need a type of Monte Carlo Minimization routine.  Scouring the Web has
turned up
> little in the way progress, so I've turned to you all in NG-Land...
>

 An interesting alternative to the suggestions already made is the approach
of the algorithm by A.Zilinskas (published as "Optimization of
one-dimensional multimodal functions", Applied Statistics 1978, v27,
p367-375 (Algorithm AS133)). This gives Fortran code, which should also be
available from statlib under directory apstat. This approach seems only
suited to 1-D problems because of the number of function evaluations. It has
the effect of balancing doing extra function evauations in regions where the
function is "roughest", with evaluations in the neighbourhoods of possibly
competing local optima. The locations where the function is evaluated are
decided so as to supply the best improvement of information about the
location of the overall optimum in a statistical sense.

However, the "genetic" algorithms already mentioned seem well suited to the
problem.



From owner-biophysics@net.bio.net Wed Oct 13 08:40:00 1999
Path: biosci!RECYCLERMAIL.COM!NetMarketing
From: NetMarketing@RECYCLERMAIL.COM
Newsgroups: bionet.biophysics
Subject: Here's Your Marketing Kit
Date: 13 Oct 1999 02:40:34 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 63
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Distribution: world
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Reply-To: N-O-More@bigfoot.com
NNTP-Posting-Host: net.bio.net

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From owner-biophysics@net.bio.net Wed Oct 13 09:05:00 1999
Path: biosci!DOGBERT.MEDIACOM.CA!kohui27
From: kohui27@DOGBERT.MEDIACOM.CA
Newsgroups: bionet.biophysics
Subject: More  Cable TV  Stations .....No Extra Charge!
Date: 13 Oct 1999 03:05:47 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 184
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <199910121427XAA34102@unlmayESPo.nabunken.go.jp>
NNTP-Posting-Host: net.bio.net

                   
This is really COOL!



ENHANCE Your Cable TV!

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?|
|?






















































d

From owner-biophysics@net.bio.net Fri Oct 15 01:54:00 1999
Path: biosci!newshost.lanl.gov!arclight.uoregon.edu!newsfeed.mathworks.com!news.maxwell.syr.edu!ameritech.net!nntp0.detroit.mi.ameritech.net.POSTED!not-for-mail
From: "Jim Kress" <jimkress@kressworks.com>
Newsgroups: comp.lang.fortran,bionet.molec-model,comp.programming,sci.math,sci.stat.math,bionet.biophysics
References: <3800F279.AD543BD3@lamar.colostate.edu>
Subject: Re: Monte Carlo Minimization Routine ???
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Xref: biosci bionet.molec-model:2757 bionet.biophysics:5275

http://dasher.wustl.edu/tinker/

--
Jim

Check out my web site  http://www.kressworks.com/
It'll blow your mind (politically), stimulate your senses (artistically)
and provide scientific insights that boggle the mind!

Ryan D. Alexander <ryanalex@lamar.colostate.edu> wrote in message
news:3800F279.AD543BD3@lamar.colostate.edu...
> In attempting to model chromosomes packed within a nucleus, I've decided
that I
> need a type of Monte Carlo Minimization routine.  Scouring the Web has
turned up
> little in the way progress, so I've turned to you all in NG-Land...
>
> Essentially I'm looking for an algorithm (in Fortran 77/90, preferably)
where I
> may enter a set of initial cartesian coordinates, the associated radii for
each
> "chromosome," and an objective function (i.e. Lennard-Jones potential
> function).  Let the program calculate the value of my objective function,
Monte
> Carlo (smartly) to re-position the chromosomes, recalculate the potential,
etc.,
> etc. until the function value is minimized.
>
> Anyone's help (books, articles, URL's) would be greatly appreciated!!  If
anyone
> in the realm of molecular dynamics, or packing theory (of non-uniform
shapes)
> have any ideas, I'd obviously welcome them as well.
>
> Thanks in advance... (oh & as this is probably not of general interest to
these
> ng's please just e-mail me directly if you'd like)
> -- Ryan D. Alexander
> =========================================================
> Ryan D. Alexander, CSU-LBNL NSCORT Ph.D. Trainee
> Colorado State Univ., Dept. of Radiological Health Sciences
> E-mail: ryanalex@lamar.colostate.edu
> Office Ph: 970-491-0520, Dept. Fax: 970-491-0623
> =========================================================
>
>



From owner-biophysics@net.bio.net Fri Oct 15 08:27:00 1999
Path: biosci!newshost.lanl.gov!arclight.uoregon.edu!hammer.uoregon.edu!newsfeed.direct.ca!su-news-hub1.bbnplanet.com!news.gtei.net!pln-w!spln!extra.newsguy.com!newsp.newsguy.com!not-for-mail
From: vjp2@smtp.dorsai.org (Vasos Panagiotopoulos +1-917-287-8087 Bioengineer-Financier)
Newsgroups: comp.lang.fortran,bionet.molec-model,comp.programming,sci.math,sci.stat.math,bionet.biophysics
Subject: Re: Monte Carlo Minimization Routine ???
Followup-To: comp.lang.fortran,bionet.molec-model,comp.programming,sci.math,sci.stat.math,bionet.biophysics
Date: 15 Oct 1999 08:24:28 GMT
Organization: Samani Marions Panyaught NYC-11357-3436-287-USA
Lines: 18
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X-Sys-Config: The configuration of my system is described in my web page. 
X-Disclaim: Nothing herein constitutes advice; everything fully disclaimed.
X-Quiet: My silence is not reluctant acquiescence rather confident deprecation.
X-URL: http://www.dorsai.org/~vjp2
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Xref: biosci bionet.molec-model:2758 bionet.biophysics:5276

There was one in SCS "Simulation" like about 1986, but there was a big
debate if the Mt Carlo made a difference. If you bug me a few days
from now, I might dig up a PL/I test program I wrote with the article
refs embedded in it.

Perhaps it can be understood by looking at a related area: In chosing
PDE solution points, Mt Carlo is said to be more effective because
beyond two dimensions, rectangularisation is inefficient. IBM's
million-dollar Simulation Blaster works along those lines by providing
a file of non-random best sampling points so you don't have to use Mt Carlo.


				- = -
Vasos-Peter John Panagiotopoulos II, Columbia'81+, Bioengineer-Financier, NYC
   BachMozart ReaganQuayle EvrytanoKastorian http://WWW.Dorsai.Org/~vjp2
               vjp2@{MCIMail.Com|CompuServe.Com|Dorsai.Org}
   ---{Nothing herein constitutes advice. Everything fully disclaimed.}---
		 [DQ2K: Make the Murky Clown Frown!]

From owner-biophysics@net.bio.net Fri Oct 15 17:28:00 1999
Path: biosci!MAIL.COM!netone1
From: netone1@MAIL.COM
Newsgroups: bionet.biophysics
Subject: INCREASE YOUR SALES WITH YOUR OWN BULK E-MAIL TOOLS
Date: 15 Oct 1999 11:28:03 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 41
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <199910151805.OAA15532@brother.com>
Reply-To: netone1@mail.com
NNTP-Posting-Host: net.bio.net

I am sure that you have gotten some e-mail advertisements since you have been online, some crazy offers and some with good offers.  They would not be sending you the ads if they were not making money.  The Internet is so big and the amount of business you could generate with bulk e-mail is limitless.  What you put into it is what you will make.
No matter what people say, bulk e-mail is here to stay, some people do not like it but you will find that the amount of people that do like it surpasses the ones that do not.

Start making that cash for the holidays!

It is a numbers game, if you e-mailed out 1 million and got a 0.001% of a response on a $10.00 product that can make you a lot of sales, say you got a minimum of 1,000 orders that will be $10,000.00 and it would only take you little time to do.  We will teach you how to use the program.

Even if you do not have a product, just sit down and think of something that you know already, like say baking cookies or how to save money on taxes or what ever you might think would sell, make up an ad and blast it.

We have a great offer for you, we have been in the bulk e-mailing business for over 2 years and have done very well and now for the first time we are offering the software to send your own bulk e-mail, and we will also throw in verified e-mail address.

The prices are as follows:

Bulk e-mail software with 7 million e-mail address $500.00
Bulk e-mail software with 4 million e-mail address  $300.00
These are the 2 packages that we offer.


All our addresses are updated on a weekly basis.

Do not delay and start making money on the Internet for yourself.  Bulk e-mailing really does work so give it a try.  We will also give you some tech support to show you how to use the software and give you tips on making up some ads for your business.

Here is some info on the bulk e-mailing program

**Extractor pro 6.1**<<---name of program
Has it's own list manager to manage your e-mail lists.  Takes duplicates out if any.(our names are duplicate free)

Has both desktop mailing capabilities and SMTP mailing capabilities.

SureSend Technology allows you to place designated e-mail addresses in each of your mailings.  After your mailing has been sent out, you can check these accounts to see if the e-mail was delivered successfully.  

Has domain removal feature to remove domains like .edu or .org etc.

Extractor Pro contains a database maintenance program that allows you to compact, repair, backup and restore your database.  

The program can send at different levels of speed depending on your computer and the size of your ad, rule of thumb 50,000 to 80,000 e-mails per hour.

Call to order or for more information 209-669-3628.  If the machine picks up please leave your name and # and the best time to call and your e-mail address.  Please state that you are calling for the software.




From owner-biophysics@net.bio.net Fri Oct 15 17:44:00 1999
Path: biosci!newsfeed.stanford.edu!logbridge.uoregon.edu!wesley.videotron.net!Pollux.Teleglobe.net!server-b.cs.interbusiness.it!news.tin.it!not-for-mail
From: "GIORGIO" <jorell@tin.it>
Newsgroups: bionet.biophysics
Subject: QQQQQQQQQQQQQQQQQ
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From owner-biophysics@net.bio.net Sun Oct 17 07:03:00 1999
Path: biosci!newsfeed.stanford.edu!newsfeed.berkeley.edu!dispose.news.demon.net!demon!newsfeed.icl.net!colt.net!diablo.theplanet.net!news.theplanet.net!newspost.theplanet.net!not-for-mail
From: "Clive Delmonte" <clivedelmonte@c-i-delmonte.freeserve.co.uk>
Newsgroups: bionet.biophysics,bionet.xtallography,sci.techniques.xtallography
Subject: DNA Structure Puzzle Number 3 -  X-Ray Diffraction from Fibres of Li-DNA
Date: Sun, 17 Oct 1999 08:57:34 +0100
Organization: Customer of Planet Online
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Xref: biosci bionet.biophysics:5279 bionet.xtallography:4961


PUZZLE NUMBER 3 - X-Ray Diffraction from Fibres of Li-DNA


Marvin et al. (5) drew fibres of the lithium salt of C-DNA in both hexagonal
and orthorhombic lattices. In a hexagonal lattice of side 3.5 nm.,
systematic absences followed (-h+k) =/=3n for l=0, and (-h+k)=3n when l=1 or
2.

Streaks were found on several layer lines in both lattices and could be
explained by molecules having a random axial translation of c/2, without
using the systematic absences, according to Marvin et al.

Fuller et al. (6) state that such a pattern of systematic absence allows the
choice of a hexagonal unit cell of side reduced by root 3. Marvin et al.
chose the larger unit cell, large enough to accommodate a double helix.

If we elect to reduce the unit cell size, a double helix cannot be
accommodated, and we find that the maximum, outer helix diameter which can
be acommodated to be:

(3.5 nm / root 3) x sin 60 x 2/3 = 1.2 nm

In an orthorhombic lattice, where Marvin et al. found a=3.22 nm and b=2.02
nm, large enough to accommodate a double helix, they report that systematic
equatorial absences follow h+k=2n+1. This pattern of absence is reported by
Langridge et al. (7) to allow the halving of the long side to form a new
reduced unit cell. In a reduced orthorhombic cell with a=2.02 nm and
b=1.61nm, a double helix cannot be accommodated, and we find that the
maximum outer diameter of a helix which can be accommodated is now 1.3 nm.

In both hexagonal and orthorhombic lattices, the observed streaks in the
patterns could result from a random axial displacement of duplexes of c/2,
according to Marvin et al. If we elect to explore the implications of a
random axial translation of c/2, utilising the layer line streaks as
evidence, we are able to use the systematic absences in both lattices to
choose a smaller unit cell in each case.

Applying Stokes' equation to the helical cross of Li DNA in the Langridge
paper (7), we find delta = 41 degrees and the helical diameter to be 1.22
nm.

A DNA helical diameter of 1.2 to 1.3 nm is therefore deducible directly from
the STM work of Lee et al. (Ref. 1) (and many other AFM & STM studies set
out in Ref. 48), or by applying Stokes' equation to Franklin's B-DNA
diffraction pattern (Ref. 3) and to diffraction from Li DNA in the C form
(7), or from James and Mazia's surface film of B-DNA (Puzzle 20 still to
come).

A very wide range of entirely separate experiments suggests that the helical
diameter of the major diffractors (the sugar-phosphate chains) is 1.2 to 1.3
nm. This dimension is dictated solely by the Watson-Crick base pair width of
1.1 nm in a true side-by-side model (see Refs. 2 & 4).

---------------------------------------------
1 Scanning Tunnelling Microscopy of Nucleic Acids; G. Lee, P.G. Arscott,
V.A. Bloomfield & D. Fennell Evans; SCIENCE Vol 244 (1989) 475 - 477

2 Towards A New Structural Molecular Biology, by Clive Delmonte, ISBN 0
9512276 0 2 (1991)

3 Molecular Configuration in Sodium Thymonucleate; R.E. Franklin &
R.G.Gosling; Nature Vol 171 (1953) 740-741

4 The Theory of X-ray Fibre Diagrams; A.R. Stokes; Prog. Biophys. & Biophys.
Chem. Vol 5 (1955) 140-167

 5 The Molecular Configuration of Deoxyribonucleic Acid. III. X-ray
Diffraction Study of the C form of the Lithium Salt; D.A. Marvin, M.
Spencer, M.H.F. Wilkins & L.D. Hamilton; J Mol Biol Vol 3 (1961) 547 - 565

6 Molecular and Crystal Structures of Double-helical RNA; W. Fuller, F.
Hutchinson, M. Spencer & M.H.F. Wilkins; J Mol Biol Vol 27 (1967) 507 - 524

7 The Molecular Configuration of Deoxyribonucleic Acid. I.; R. Langridge,
H.R. Wilson, C.W. Hooper, M.H.F. Wilkins & L.D. Hamilton; J Mol Biol Vol 2
(1960) 19-37
----------------------------------------------------------
Clive Delmonte

For a view of all the DNA Structure Puzzles
and the DNA publications, please refer to:
http://www.c-i-delmonte.freeserve.co.uk



From owner-biophysics@net.bio.net Sun Oct 17 08:00:00 1999
Path: biosci!internet!biosci!not-for-mail
From: biohelp (BIOSCI Administrator)
Newsgroups: bionet.biophysics
Subject: BIOSCI/bionet miniFAQ & Fundraiser
Date: 17 Oct 1999 02:00:11 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 239
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <199910170900.CAA26470@net.bio.net>
NNTP-Posting-Host: net.bio.net


(LAST REVISION: 14-AUG-99)

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.
--------------------------------------------------------
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
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Please check your database entry from time-to-time to see if your
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resources to edit old forms.






From owner-biophysics@net.bio.net Mon Oct 18 23:23:00 1999
Path: biosci!newshost.lanl.gov!logbridge.uoregon.edu!su-news-hub1.bbnplanet.com!paloalto-snf1.gtei.net!news.gtei.net!webtv.net!not-for-mail
From: degby@webtv.net (Don E.J.G. Beggs)
Newsgroups: bionet.biophysics
Subject: Pulsed magnet vagus nerve stimulation?
Date: Mon, 18 Oct 1999 16:43:36 -0700 (PDT)
Organization: WebTV Subscriber
Lines: 6
Message-ID: <28719-380BB0A8-80@storefull-152.iap.bryant.webtv.net>
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Content-Disposition: Inline

Why not use pulsed magnet vagus nerve stimulation as used to stimulate
the brain without invasive surgery to implant electrodes?


db


From owner-biophysics@net.bio.net Tue Oct 19 14:23:00 1999
Path: biosci!FLASHMAIL.COM!selaa
From: selaa@FLASHMAIL.COM
Newsgroups: bionet.biophysics
Subject: We Will Pay Your Bills
Date: 19 Oct 1999 08:23:42 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 110
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Message-ID: <000013481cc8$000002a7$00003df1@ramada.co.il>
Reply-To: selaa@flashmail.com
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From owner-biophysics@net.bio.net Tue Oct 19 15:25:00 1999
Path: biosci!263.NET!gulululu
From: gulululu@263.NET ("Hong Wang")
Newsgroups: bionet.biophysics
Subject: (none)
Date: 19 Oct 1999 09:25:24 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
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From owner-biophysics@net.bio.net Tue Oct 19 23:39:00 1999
Path: biosci!FYS.KU.DK!thomas
From: thomas@FYS.KU.DK (Thomas Zaccarin Lauritzen)
Newsgroups: bionet.biophysics
Subject: (none)
Date: 19 Oct 1999 17:39:30 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
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NNTP-Posting-Host: net.bio.net

unsubscribe


From owner-biophysics@net.bio.net Wed Oct 20 00:44:00 1999
Path: biosci!newsfeed.stanford.edu!logbridge.uoregon.edu!newsfeed.icl.net!diablo.theplanet.net!colt.net!Pollux.Teleglobe.net!server-b.cs.interbusiness.it!news.tin.it!not-for-mail
From: "Rambo" <gpascol@tin.it>
Newsgroups: bionet.biophysics
Subject: 2333333333333333333333333333
Date: Mon, 18 Oct 1999 04:46:56 +0200
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From owner-biophysics@net.bio.net Wed Oct 20 08:07:00 1999
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From: mmerckel@btk.utu.fi (Michael Merckel)
Newsgroups: bionet.biophysics
Subject: AHA ? Re: KKKKKKKKKKKKKKKKK
Date: 20 Oct 1999 10:00:30 +0100
Organization: MRC Human Genome Mapping Project Resource Centre
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Has the internet reached critical mass ?

Are we witnessing the evolution of a new
digital lifeform learning to speak via SMTP
and only the Subject line ?

Beware the day it discovers the BODY of the email.


---

From owner-biophysics@net.bio.net Wed Oct 20 09:42:00 1999
Path: biosci!263.NET!howie_wang
From: howie_wang@263.NET ("Hong Wang")
Newsgroups: bionet.biophysics
Subject: DNA hybridization Molecular Simulation
Date: 20 Oct 1999 03:42:46 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
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From owner-biophysics@net.bio.net Wed Oct 20 10:40:00 1999
Path: biosci!newshost.lanl.gov!awabi.library.ucla.edu!128.230.129.106!news.maxwell.syr.edu!tank.news.pipex.net!pipex!server1.netnews.ja.net!hgmp.mrc.ac.uk!biosci
From: TIY@phys.chem.msu.ru (Ivan Torshin)
Newsgroups: bionet.biophysics
Subject: [Fwd: The Abundance of Spam Mail]
Date: 20 Oct 1999 12:33:24 +0100
Organization: MSU Chem dept
Lines: 63
Message-ID: <380DB63E.57D0DF50@phys.chem.msu.ru>
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This is a multi-part message in MIME format.
--------------79E3985D1E91FF478A381996
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Just to mention some means...
--------------79E3985D1E91FF478A381996
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Received: by beta.chem.msu.ru (mbox b178)
 (with Cubic Circle's cucipop (v1.31 1998/05/13) Wed Jul 14 20:31:25 1999)
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From: "Chad C. Sines" <chad.sines@chemistry.gatech.edu>
Subject: The Abundance of Spam Mail
Date: Wed, 14 Jul 1999 04:24:10 -0700
Organization: Georgia Institute of Technology
Message-ID: <378C735A.D7A0CCF3@chemistry.gatech.edu>
To: x-plor@hgmp.mrc.ac.uk, xtal-log@hgmp.mrc.ac.uk
Sender: owner-xtal-log@hgmp.mrc.ac.uk
Precedence: bulk

This is a little off topic I know, but I feel it is relevant.  I am a
crystallographer and a frequenter of three main crystallographic news
groups, this being one.  Mostly I read the postings, but I do
occassionally post or respond to them.  I have been very annoyed at the
amount of spam postings we have received.  I have also been receiving
many to my email address apparently from some louse grabbing my email
address from postings.

I have found a FREE reporting mechanism at http://spamcop.net/  I
stumbled upon it by accident.  It will make all the necessary reports to
network administrators concerning spam email and newsgrou postings.  It
is able to get through phony email addresses by reading the headers.  It
takes me less than a minute to do this and I have received responses
from the administrators with news that the person had been dealt with.

It's just a thought.  If spamming doesn't bother you, then I am sorry to
have bugged you.

Chad


--------------79E3985D1E91FF478A381996--

---

From owner-biophysics@net.bio.net Wed Oct 20 12:07:00 1999
Path: biosci!newsfeed.stanford.edu!logbridge.uoregon.edu!wesley.videotron.net!Pollux.Teleglobe.net!server-b.cs.interbusiness.it!news.tin.it!not-for-mail
From: "Rambo" <gpascol@tin.it>
Newsgroups: bionet.biophysics
Subject: 999999999999999999999999999
Date: Mon, 18 Oct 1999 12:26:37 +0200
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NNTP-Posting-Host: 212.216.168.131
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From owner-biophysics@net.bio.net Wed Oct 20 14:26:00 1999
Path: biosci!newsfeed.stanford.edu!newsfeed.berkeley.edu!news-feed.ifi.uio.no!uninett.no!newscore.univie.ac.at!aconews.univie.ac.at!news.univie.ac.at!not-for-mail
From: Seminar03 <kurs03.seminar@akh-wien.ac.at>
Newsgroups: bionet.biophysics
Subject: Automobil,bionet biophysiks
Date: Wed, 20 Oct 1999 17:05:01 +0200
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Liebe Gita
 Ich schicke dir den Text
hhhhhhhhhhhhh

--
md. sayedul haq



From owner-biophysics@net.bio.net Wed Oct 20 14:29:00 1999
Path: biosci!newsfeed.stanford.edu!newsfeed.berkeley.edu!dispose.news.demon.net!demon!newsfeed.icl.net!newsfeed.nacamar.de!fu-berlin.de!newscore.univie.ac.at!newsfeed03.univie.ac.at!news.univie.ac.at!not-for-mail
From: Seminar03 <kurs03.seminar@akh-wien.ac.at>
Newsgroups: bionet.biophysics
Subject: Text biophysiks bionet
Date: Wed, 20 Oct 1999 17:07:36 +0200
Organization: IMC
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Liebe Gita!
hhhhhhhhhhhhhhhh

--
md. sayedul haq



From owner-biophysics@net.bio.net Wed Oct 20 15:28:00 1999
Path: biosci!neuro.mpg.de!sidney
From: sidney@neuro.mpg.de (Sidney Cambridge)
Newsgroups: bionet.biophysics
Subject: Diffusion of dextrans compared to proteins ?
Date: 20 Oct 1999 09:28:48 -0700
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Hi, all,

*Unfortunately* I have to estimate the diffusion of an antibody in brain
slices. I figured a quick way of doing is would be to determine the
diffusion of a fluorescently labeled dextran (with a caged fluorescent
dye) with comperable diffusion characteristics. I vaguely remember
hearing that dextrans diffuse like proteins three times their size (i.e.
a 30kD dextran diffuses like a 90kD protein). I couldn't find any
literature on this so I thought maybe I could get some help here. So,
does anybody know how dextrans compare to proteins in respect to
diffusion ?

Thank you very much in advance.

Sidney

sidney@neuro.mpg.de




From owner-biophysics@net.bio.net Thu Oct 21 09:03:00 1999
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From: gussak@agri.gov.il (Eugene Gussakovsky)
Newsgroups: bionet.biophysics
Subject: FEBS web site
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I should greatly appreciate to everybody who send me web site address of
FEBS (FedEurBiochemSoc). Thanks in advance.
Eugene

---

From owner-biophysics@net.bio.net Thu Oct 21 09:13:00 1999
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From: Frank Fuerst <ffrank@rz.uni-potsdam.de>
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Subject: Re: FEBS web site
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Eugene Gussakovsky wrote:
> 
> I should greatly appreciate to everybody who send me web site address of
> FEBS (FedEurBiochemSoc). Thanks in advance.
> Eugene

http://www.febs.unibe.ch/

Frank
-- 
Hi! I'm Norton Antivirus. Replace your signature with this text for
protection against Signature Virus 99 and many others.

From owner-biophysics@net.bio.net Thu Oct 21 13:52:00 1999
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From: nerais@gmx.de (Akin Akkoyun )
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Subject: Re: Diffusion of dextrans compared to proteins ?
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On 20 Oct 1999 09:28:48 -0700, sidney@neuro.mpg.de (Sidney Cambridge)
wrote:

I am not sure , you can compare the Dextran with your AB. Your are
working in tissue and "cross-reactions" will be different. 

Why not labelling your AB with a Fluorescent dye ?? Labelling kits, or
activated Fluorescent molecules are available from everywhere in any
colour .  That's quite easy .. 

>Hi, all,
>
>*Unfortunately* I have to estimate the diffusion of an antibody in brain
>slices. I figured a quick way of doing is would be to determine the
>diffusion of a fluorescently labeled dextran (with a caged fluorescent
>dye) with comperable diffusion characteristics. I vaguely remember
>hearing that dextrans diffuse like proteins three times their size (i.e.
>a 30kD dextran diffuses like a 90kD protein). I couldn't find any
>literature on this so I thought maybe I could get some help here. So,
>does anybody know how dextrans compare to proteins in respect to
>diffusion ?
>
>Thank you very much in advance.
>
>Sidney
>
>sidney@neuro.mpg.de
>
>
>


From owner-biophysics@net.bio.net Fri Oct 22 18:06:00 1999
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From: "Clive Delmonte" <clivedelmonte@c-i-delmonte.freeserve.co.uk>
Newsgroups: bionet.biophysics,bionet.xtallography,sci.techniques.xtallography
Subject: DNA Structure Puzzle Number 4 -  X-Ray Diffraction from a Fibre of DNA-polyarginine
Date: Fri, 22 Oct 1999 19:31:59 +0100
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Xref: biosci bionet.biophysics:5301 bionet.xtallography:4973

PUZZLE NUMBER 4     X-Ray Diffraction from a Fibre of DNA-polyarginine


Suwalski & Traub (8) studied a fibre of the DNA-polyarginine complex by
X-ray diffraction. Their diffraction pattern shows "pronounced streaks" in a
hexagonal lattice of side 4.15 nm and they remarked that the equatorial
reflections followed h x h + h x k + k x k = 3n.

This pattern of equatorial presences is equivalent to that of Fuller et al.
(Puzzle #3, Ref.6) where such presences follow h-k=3n in a cell whose side
can be reduced by root 3. (Squaring (h-k) and subtracting from the
expression in the previous paragraph, there is a difference of 3hk, a
quantity always divisible by 3.) Therefore Suwalski & Traub's value of 'a'
can reduced by root 3.

Suwalski and Traub decided that their pattern of systematic absence could be
explained by postulating axial translations of the molecules equal to c/3.

Now, the very same diffraction pattern of Suwalski and Traub with
DNA-polyarginine was re-indexed on an orthogonal net by Fita et al. (9) in a
unit cell of approximate section 2.6 nm x 3.6 nm (10) where equatorial
reflections followed h+k = 2n.

Langridge et al. (Puzzle #3, Ref. 7) have shown that this pattern of
presences would allow the halving of the long side of the cell section.

Fita et al. considered that the pattern of systematic absences in their
orthogonal net indicated that the axial translation of the molecules was
c/4.

So Suwalski & Traub considered that the fibre had axial displacements of the
molecules of c/3 in a hexagonal net, and Fita et al. found the axial
displacement to be c/4 in an orthogonal net.

But there was only one single fibre and only one diffraction pattern.

Therefore, whether a hexagonal or orthogonal array is chosen, the axial
dispacement can only have one value.

Marvin et al. (Puzzle #3, Ref. 5) considered that a random axial translation
of their molecules of c/2 would account for the streaks on their layer lines
in a hexagonal lattice.

The value common to both analyses is therefore c/2, but this is deducible
from the layer line streaks and not from the patterns of systematic absence.

Therefore the patterns of systematic absence in both the hexagonal and
orthogonal nets should be taken to show that, for both indexing schemes, a
smaller unit cell is the right choice, with a random axial displacement of
c/2.

However, if the unit cell sizes are reduced accordingly, the double helix
can no longer be fitted into the reduced dimensions of the original cells.

As we have seen in the earlier Puzzles, a true side-by-side duplex, where
each helix has a diameter of about 1.3 nm, and, in this case, has its
grooves at least partially filled with poly-arginine, will fit the new,
reduced unit cells (e-mail author for diagram). The helical diameter of
about 1.3 nm is a direct geometric consequence of the Watson-Crick base pair
width of 1.1 nm.
------------------------------------------
8 A Comparative X-ray Study of a Nucleoprotamine & DNA Complexes with
Polylysine & Polyarginine; M. Suwalski & W. Traub; Biopol. Vol 11 (1972)
2223 - 2231

9 X-ray Diffraction Study of DNA Complexes with Arginine Peptides and Their
Relation to Nucleoprotamine Structure; I. Fita, J.L. Campos, L.C. Puigjaner
& J.A. Subirana; J Mol Biol Vol 167 (1983) 157 - 177

10 X-ray Diffraction Studies of Nucleoprotamine Structure; P. Suau & J.A.
Subirana; J Mol Biol Vol 117 (1977) 909 - 926




Clive Delmonte

For a view of all the DNA Structure Puzzles
and the DNA publications, please refer to:
http://www.c-i-delmonte.freeserve.co.uk



From owner-biophysics@net.bio.net Sat Oct 23 23:59:00 1999
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From: Wolf@your.mom.com (Wolf)
Newsgroups: bionet.biophysics
Subject: radiation and gycerol stock
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Hello People...



I just find out that my E.Coli and yeast glycerol stocks in -80
freezer have been exposed to high radiation by 59Fe for more than  2
months.  The radioactivity is still very very high.

Is it possible to have any effects on my glycerol stock from radiation
such as mutation or whatever possible damage?

Thank you very much for any comments.

From owner-biophysics@net.bio.net Sat Oct 23 23:59:00 1999
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From: Wolf@your.mom.com (Wolf)
Newsgroups: bionet.biophysics
Subject: radiation and DNA damage
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Hello People...



I just find out that my E.Coli and yeast glycerol stocks in -80
freezer have been exposed to high radiation by 59Fe for more than  2
months.  The radioactivity is still very very high.

Is it possible to have any effects on my glycerol stock from radiation
such as mutation or whatever possible damage?

Thank you very much for any comments.

From owner-biophysics@net.bio.net Sun Oct 24 19:29:00 1999
Path: biosci!newsfeed.stanford.edu!newsfeed.berkeley.edu!newsfeed2.news.nl.uu.net!sun4nl!uunet!ams.uu.net!iafrica.com!nnrp01.iafrica.com!nnrp01.iafrica.com!not-for-mail
From: Robert <rloc@iafrica.com>
Newsgroups: bionet.biophysics
Subject: Re: Bioprobe 1966
Date: Mon, 25 Oct 1999 00:21:14 +0200
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This may not be the correct forum for my enquiry and I hope this will not
offend the users of this newsgroup.
In 1966 Goddard Space center launched what was to be the first of  a series
of biological probes destined for altitudes in excess of 100kM above the
earth.  The probe was called Bioprobe_1. The intention was to detect any
life forms at this extreme altitude.

I have not yet been able to examine the results of this experiment and I
therefore would appreciate any input from this forum as to the final
outcome of this experiment.

Please reply to: rloc@usa.net

Thank you


From owner-biophysics@net.bio.net Mon Oct 25 07:01:00 1999
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From: "Clive Delmonte" <clivedelmonte@c-i-delmonte.freeserve.co.uk>
Newsgroups: bionet.biophysics,bionet.xtallography,sci.techniques.xtallography
Subject: DNA Structure Puzzle Number 4 -  X-Ray Diffraction from a Fibre of DNA-polyarginine
Date: Mon, 25 Oct 1999 08:55:55 +0100
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Xref: biosci bionet.biophysics:5310 bionet.xtallography:4976

PUZZLE NUMBER 4     X-Ray Diffraction from a Fibre of DNA-polyarginine

Suwalski & Traub (8) studied a fibre of the DNA-polyarginine complex by
X-ray diffraction. Their diffraction pattern shows "pronounced streaks" in a
hexagonal lattice of side 4.15 nm and they remarked that the equatorial
reflections followed h x h + h x k + k x k = 3n.

This pattern of equatorial presences is equivalent to that of Fuller et al.
(Puzzle #3, Ref.6) where such presences follow h-k=3n in a cell whose side
can be reduced by root 3. (Squaring (h-k) and subtracting from the
expression in the previous paragraph, there is a difference of 3hk, a
quantity always divisible by 3.) Therefore Suwalski & Traub's value of 'a'
can reduced by root 3.

Suwalski and Traub decided that their pattern of systematic absence could be
explained by postulating axial translations of the molecules equal to c/3.

Now, the very same diffraction pattern of Suwalski and Traub with
DNA-polyarginine was re-indexed on an orthogonal net by Fita et al. (9) in a
unit cell of approximate section 2.6 nm x 3.6 nm (10) where equatorial
reflections followed h+k = 2n.

Langridge et al. (Puzzle #3, Ref. 7) have shown that this pattern of
presences would allow the halving of the long side of the cell section.

Fita et al. considered that the pattern of systematic absences in their
orthogonal net indicated that the axial translation of the molecules was
c/4.

So Suwalski & Traub considered that the fibre had axial displacements of the
molecules of c/3 in a hexagonal net, and Fita et al. found the axial
displacement to be c/4 in an orthogonal net.

But there was only one single fibre and only one diffraction pattern.

Therefore, whether a hexagonal or orthogonal array is chosen, the axial
dispacement can only have one value.

Marvin et al. (Puzzle #3, Ref. 5) considered that a random axial translation
of their molecules of c/2 would account for the streaks on their layer lines
in a hexagonal lattice.

The value common to both analyses is therefore c/2, but this is deducible
from the layer line streaks and not from the patterns of systematic absence.

Therefore the patterns of systematic absence in both the hexagonal and
orthogonal nets should be taken to show that, for both indexing schemes, a
smaller unit cell is the right choice, with a random axial displacement of
c/2.

However, if the unit cell sizes are reduced accordingly, the double helix
can no longer be fitted into the reduced dimensions of the original cells.

As we have seen in the earlier Puzzles, a true side-by-side duplex, where
each helix has a diameter of about 1.3 nm, and, in this case, has its
grooves at least partially filled with poly-arginine, will fit the new,
reduced unit cells (e-mail author for diagram). The helical diameter of
about 1.3 nm is a direct geometric consequence of the Watson-Crick base pair
width of 1.1 nm.
------------------------------------------
8 A Comparative X-ray Study of a Nucleoprotamine & DNA Complexes with
Polylysine & Polyarginine; M. Suwalski & W. Traub; Biopol. Vol 11 (1972)
2223 - 2231

9 X-ray Diffraction Study of DNA Complexes with Arginine Peptides and Their
Relation to Nucleoprotamine Structure; I. Fita, J.L. Campos, L.C. Puigjaner
& J.A. Subirana; J Mol Biol Vol 167 (1983) 157 - 177

10 X-ray Diffraction Studies of Nucleoprotamine Structure; P. Suau & J.A.
Subirana; J Mol Biol Vol 117 (1977) 909 - 926




Clive Delmonte

For a view of all the DNA Structure Puzzles
and the DNA publications, please refer to:
http://www.c-i-delmonte.freeserve.co.uk


--
Clive Delmonte

For a view of all the DNA Structure Puzzles
and the DNA publications, please refer to:
http://www.c-i-delmonte.freeserve.co.uk



From owner-biophysics@net.bio.net Mon Oct 25 12:27:00 1999
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From: skq1@my-deja.com
Newsgroups: bionet.biophysics
Subject: Pulsed Power Technology In Medicine
Date: Mon, 25 Oct 1999 13:12:51 GMT
Organization: Deja.com - Before you buy.
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PULSED POWER 2000
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Wednesday 3 - Thursday 4 May 2000

On behalf of the Institution of Electrical Engineers (IEE), based in
the UK, I would like to draw your attention to the forthcoming 'PULSED
POWER 2000' symposium, which will be held in London on 3-4 May 2000.
This event will provide an invaluable opportunity for you to:

1.  network with your contemporaries in industry and in research. 2.
publicise your company and what it offers.
3.  present a paper on an area of pulsed power technology.

This event is held annually and attracts upwards of 100 delegates.  It
provides a forum for information interchange between industry, academia
and research establishments on a broad range of current and emerging
research areas of pulsed power technology.  There will be a series of
oral presentations and keynote speeches accompanied by company
exhibitions and poster sessions.  There will also be considerable
opportunity for technical discussion and for networking - a symposium
dinner will be held on 3 May 2000.

Papers are welcomed for both oral and poster sessions on:
1.  novel, compact, high repetition rate or high energy pulsed power
supplies
2.  solid state and spark gap switches
3.  gaseous, liquid and solid insulation studies
4.  high speed diagnostics
5.  computational techniques
6.  applications of pulsed power including high energy physics,
environmental, EM launchers, medical, radiation sources, high power
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If you wish to be added to the mailing list please send an email to
squreshi@iee.org.uk quoting reference PP2000/NG.

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enquiries should be communicated by email to squreshi@iee.org.uk

If you would like to make a technical contribution please submit an
abstract of not more than 200 words, quoting reference CFP/NG to Mr
Chris Spikings, British Aerospace Sowerby Research Centre, FPC 30, PO
Box 5, Filton, Bristol, UK, BS34 7QW or email
chris.spikings@src.bae.co.uk


Sent via Deja.com http://www.deja.com/
Before you buy.

From owner-biophysics@net.bio.net Mon Oct 25 14:30:00 1999
Path: biosci!NETDOME.COM!pauluzzi
From: pauluzzi@NETDOME.COM ("ICIE Y2K")
Newsgroups: bionet.biophysics
Subject: =?iso-8859-1?Q?VI_Congreso_Internacional_de_Ingenieria_Inform=E1tica?=
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This is a multi-part message in MIME format.

------=_NextPart_000_0318_01BF1EE3.4F420740
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                    VI Congreso Internacional de Ingenieria =
Inform=E1tica
                                            April 26-28, 2000
                                                    ICIE Y2K

First Call for Papers

This Congress is organized by the Department of Computer Science, School =
of
Engineering of the University of Buenos Aires. The aim of the Congress =
is to
build a forum to discuss recent advances in computer science and =
information
technology. Theoretical and empirical papers are particulary welcomed. =
The
subject areas can be (but are not limited to) the following:

ACKNOWLEDGEMENT BASED SYSTEMS - NEURAL NETWORKS - DIFFUSSED SYSTEMS -
ARTIFICIAL INTELLIGENCE - DATABASES - COMPUTATIONAL ALGEBRA - =
COMPUTATIONAL
LANGUAGES - OBJECT ORIENTED TECHNOLOGY - MULTIMEDIA -
VISION THROUGH COMPUTERS - ROBOTICS -
EDUCATION AT INFORMATICS - SOFTWARE ENGINEERING - OPERATIONS RESEARCH
DISTRIBUTED -
SYSTEMS, NETWORKS REAL-TIME SYSTEMS.

Please send 3 copies of the final version of your complete paper to the
committee address given below. In addition, send an electronic copy of =
your
paper (either in Microsoft Word 97 - .DOC or .RTF format). The =
electronic
copy can be sent either by e-mail to iciey2k@mara.fi.uba.ar  or as a
diskette (or CD-ROM) by regular mail to the comittee address.

COMMITTEE ADDRESS:
Comit=E9 de Programa ICIE Y2K.
Departamento de Computaci=F3n.
Facultad de Ingenier=EDa.
Universidad de Buenos Aires.
Paseo Col=F3n 850. 4to. Piso (1063).
Capital Federal. Argentina.

Your paper must have the following format:
Arial or Times New Roman font of 12 points
Single spaced, not to exceed 15 pages (A4 size)
The margins should be 2,54 cm (1 inch) on all sides

The cover page should contain the title of the paper, first name, last =
name
(please type the last name in CAPITAL letters), affiliation, full =
address,
and e-mail of the author(s), along with the application area(s) that =
best
describes the paper. Please also provide a short biograph of the =
author(s)
at the end of the paper. Throughout the paper, please avoid any headers,
footnotes and page numbers. Papers not meeting the above requirements =
will
not be considered.

IMPORTANT DEADLINES:
Complete paper due date: February 1, 2000
Acceptance notifications will be sent out on or after March 1, 2000.

Papers received after February 1 deadline may not be included in the
proceedings.

COPYRIGHT:

Author(s) whose paper(s) has been accepted, implicitly transfer the
copyright to the School of Engineering (S.O.E.), University of Buenos =
Aires
and authorize S.O.E. to publish that paper(s) in the proceedings of ICIE =
Y2K
Congress.


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<!DOCTYPE HTML PUBLIC "-//W3C//DTD HTML 4.0 Transitional//EN">
<HTML><HEAD>
<META content=3D"text/html; charset=3Diso-8859-1" =
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<STYLE></STYLE>
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<BODY bgColor=3D#ffffff>
<DIV><FONT face=3DArial size=3D2>
<DIV><FONT face=3DArial=20
size=3D2>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbs=
p;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;=20
VI Congreso Internacional de Ingenieria=20
Inform=E1tica<BR>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&n=
bsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nb=
sp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbs=
p;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;=20
April 26-28,=20
2000<BR>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp=
;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;=
&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&=
nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&n=
bsp;&nbsp;&nbsp;&nbsp;=20
ICIE Y2K<BR><BR>First Call for Papers<BR><BR>This Congress is organized =
by the=20
Department of Computer Science, School of<BR>Engineering of the =
University of=20
Buenos Aires. The aim of the Congress is to<BR>build a forum to discuss =
recent=20
advances in computer science and information<BR>technology. Theoretical =
and=20
empirical papers are particulary welcomed. The<BR>subject areas can be =
(but are=20
not limited to) the following:<BR><BR>ACKNOWLEDGEMENT BASED SYSTEMS - =
NEURAL=20
NETWORKS - DIFFUSSED SYSTEMS -<BR>ARTIFICIAL INTELLIGENCE - DATABASES -=20
COMPUTATIONAL ALGEBRA - COMPUTATIONAL<BR>LANGUAGES - OBJECT ORIENTED =
TECHNOLOGY=20
- MULTIMEDIA -<BR>VISION THROUGH COMPUTERS - ROBOTICS -<BR>EDUCATION AT=20
INFORMATICS - SOFTWARE ENGINEERING - OPERATIONS RESEARCH<BR>DISTRIBUTED=20
-<BR>SYSTEMS, NETWORKS REAL-TIME SYSTEMS.<BR><BR>Please send 3 copies of =
the=20
final version of your complete paper to the<BR>committee address given =
below. In=20
addition, send an electronic copy of your<BR>paper (either in Microsoft =
Word 97=20
- .DOC or .RTF format). The electronic<BR>copy can be sent either by =
e-mail to=20
<A =
href=3D"mailto:iciey2k@mara.fi.uba.ar">iciey2k@mara.fi.uba.ar</A>&nbsp; =
or as=20
a<BR>diskette (or CD-ROM) by regular mail to the comittee=20
address.<BR><BR>COMMITTEE ADDRESS:<BR>Comit=E9 de Programa ICIE=20
Y2K.<BR>Departamento de Computaci=F3n.<BR>Facultad de =
Ingenier=EDa.<BR>Universidad=20
de Buenos Aires.<BR>Paseo Col=F3n 850. 4to. Piso (1063).<BR>Capital =
Federal.=20
Argentina.<BR><BR>Your paper must have the following format:<BR>Arial or =
Times=20
New Roman font of 12 points<BR>Single spaced, not to exceed 15 pages (A4 =

size)<BR>The margins should be 2,54 cm (1 inch) on all sides<BR><BR>The =
cover=20
page should contain the title of the paper, first name, last =
name<BR>(please=20
type the last name in CAPITAL letters), affiliation, full =
address,<BR>and e-mail=20
of the author(s), along with the application area(s) that =
best<BR>describes the=20
paper. Please also provide a short biograph of the author(s)<BR>at the =
end of=20
the paper. Throughout the paper, please avoid any headers,<BR>footnotes =
and page=20
numbers. Papers not meeting the above requirements will<BR>not be=20
considered.<BR><BR>IMPORTANT DEADLINES:<BR>Complete paper due date: =
February 1,=20
2000<BR>Acceptance notifications will be sent out on or after March 1,=20
2000.<BR><BR>Papers received after February 1 deadline may not be =
included in=20
the<BR>proceedings.<BR><BR>COPYRIGHT:<BR><BR>Author(s) whose paper(s) =
has been=20
accepted, implicitly transfer the<BR>copyright to the School of =
Engineering=20
(S.O.E.), University of Buenos Aires<BR>and authorize S.O.E. to publish =
that=20
paper(s) in the proceedings of ICIE=20
Y2K<BR>Congress.<BR></FONT></DIV></FONT></DIV></BODY></HTML>

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From owner-biophysics@net.bio.net Mon Oct 25 18:29:00 1999
Path: biosci!newshost.lanl.gov!logbridge.uoregon.edu!newsfeed.direct.ca!news.idt.net!nntp.farm.idt.net!news
From: "NDRI/HBDI" <hbdi@idt.net>
Newsgroups: alt.bio.technology,alt.bio.technology.misc,bionet,bionet.biology,bionet.biophysics,bionet.cellbiol
Subject: Autopsy, Surgical Discard and Transplantation Tissues for Now Available for Research
Date: Mon, 25 Oct 1999 15:16:27 -0400
Organization: IDT (Best News In The World)
Lines: 16
Message-ID: <7v2aav$bhu@nnrp3.farm.idt.net>
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Xref: biosci bionet.biophysics:5313 bionet.cellbiol:12737

See www.ndri.com for access to human tissues and organs for medical
researchers

See www.hbdi.org for information about family collections containing DNA and
immortalized cells - over 600 families - for medical and genetic researchers


NDRI and HBDI are non-profit organizations aiding medical research and the
search for disease genes.








From owner-biophysics@net.bio.net Tue Oct 26 09:07:00 1999
Path: biosci!ppgnpqqclnk.ex-press.ru!khkgjfhd
From: khkgjfhd@ppgnpqqclnk.ex-press.ru
Newsgroups: bionet.biophysics
Subject: FREE Pagers -tjhihliumc
Date: 26 Oct 1999 03:06:54 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
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                                   FREE PAGER

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From owner-biophysics@net.bio.net Wed Oct 27 02:09:00 1999
Path: biosci!rutgers!gatech!newsfeed.mathworks.com!news.maxwell.syr.edu!nntp2.deja.com!nnrp1.deja.com!not-for-mail
From: MisterScience@altavista.net
Newsgroups: bionet.biophysics,bionet.microbiology,sci.bio.microbiology,bionet.cellbiol
Subject: Important Science Vote
Date: Wed, 27 Oct 1999 02:46:23 GMT
Organization: science
Lines: 31
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Xref: biosci bionet.biophysics:5315 bionet.microbiology:17911 bionet.cellbiol:12739

A vote is going on at Amazon.com for the best book of the millennium.
It would be nice if a science book was selected. If we pool our efforts
and vote in unison then maybe we can succeed. I've searched through
the top-selling science books and I suggest that we vote for "The Bible
According to Einstein: A Scientific Complement to the Holy Bible for
the Third Millennium." Being a comprehensive summary of all scientific
knowledge of the last two thousand years, it seems an appropriate
choice.

To vote go to http://www.amazon.com/ and click on "Enter to win."

For the title entry, "The Bible According to Einstein" should suffice.
There is no author listed for the book so leave that space blank.
By the way, by voting you become eligible
for Amazon.com's millennium giveaway contest.

Tell your science friends to vote too.

Long live science!
Mister Science






-----------------------------------------------------------------


Sent via Deja.com http://www.deja.com/
Before you buy.

From owner-biophysics@net.bio.net Wed Oct 27 07:01:00 1999
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From: "Donovan Porter" <donovan@molbiol.uct.ac.za>
Newsgroups: bionet.biophysics,bionet.microbiology,sci.bio.microbiology,bionet.cellbiol
Subject: Re: Important Science Vote
Date: Wed, 27 Oct 1999 09:52:13 +0200
Organization: Adamastor
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