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Subject: transcription problem
To: rna@net.bio.net (rna)
Date: Sat, 1 Apr 1995 15:21:35 -0700 (MST)
From: "Douglas J Bucklin" <bucklin@selway.umt.edu>
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Netters:

	We are trying to synthesize several RNAs.  For most we have no problem, 
but two of them are giving us problems.
	The two troublesome ones break down into one that works O.K., 
and another that is quite similar, but will not appear.  We transcribe 
off of oligo templates with T7 RNA Pol. and use the protocol of 
Milligan(sp?) et al. (NAR, late 80's) for the reactions.  Both RNAs are 
designed to be stem and loop structures.  The sequences are virtually 
identicle, the one that works does have five extra nucleotides at the 
3' end that are not involved in the stem loop.  All of the other bases, 
for both RNAs, are in the stem loop.  The first three nucleotides 
incorporated are G.
	We have tried templates that are ds only in the promoter region, 
and fully ds templates.
	Do any of you have any ideas why two nearly identicle templates 
would give these results?  Do you have suggestions to provide that may 
aid in getting the troublesome template to produce?

Thank you
Douglas Bucklin
bucklin@selway.umt.edu


From BIOSCI-REQUEST  Sat Apr  1 17:18:20 1995
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Subject: transcription II
To: rna@net.bio.net (rna)
Date: Sat, 1 Apr 1995 18:18:06 -0700 (MST)
From: "Douglas J Bucklin" <bucklin@selway.umt.edu>
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Netters:

	I have a second question regarding trascription.  After carrying 
out large scale transcriptions, with the goal of getting approx. 20 
nmoles of transcript, what is a good method of purification.  Currently 
we are using gel purification on 3mm polyacryl., 7M urea, TBE gels or 
biospin exclusion columns.  I really don't like any of the methods I have 
found.  They are usually labor intensive.  Is there something out there 
that is quick and reliable.
	When doing the transcriptions there is often a heavy amount of 
insoluble goo that is produced.  We have found that the RNA is in that 
fraction.  Is that a common experience?  How do you redissolve that 
fraction?  Even after heating and diluting the scum still likes to 
persist.  

Thank you
Douglas Bucklin
bucklin@selway.umt.edu


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From: dcs@neutron.chem.yale.edu (Dave Schweisguth)
Message-Id: <199504021430.KAA26473@neutron.chem.yale.edu>
Subject: Re: transcription II
To: rna@net.bio.net (RNA mailing list)
Date: Sun, 2 Apr 1995 10:30:58 -0400 (EDT)
In-Reply-To: <9504020118.AA18543@selway.umt.edu> from "Douglas J Bucklin" at Apr 1, 95 06:18:06 pm
Organization: Dept. of Chemistry, Yale University
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Doug,

> 	I have a second question regarding trascription.  After carrying out
> large scale transcriptions, with the goal of getting approx. 20 nmoles of
> transcript, what is a good method of purification.  Currently we are using
> gel purification on 3mm polyacryl., 7M urea, TBE gels or biospin exclusion
> columns.  I really don't like any of the methods I have found.  They are
> usually labor intensive.  Is there something out there that is quick and
> reliable.

Our lab (which does several-micromole-scale preps for NMR) mostly uses
polyacrylamide. Some of us (including me) use HPLC, which is lovely when it
works but requires occasional lengthy periods of tinkering. Our usual column
is a DEAE 60-7 from Nucleogen (via Rainin).

> 	When doing the transcriptions there is often a heavy amount of
> insoluble goo that is produced.  We have found that the RNA is in that
> fraction.  Is that a common experience?  How do you redissolve that
> fraction?  Even after heating and diluting the scum still likes to persist.

That's magnesium pyrophosphate. Redissolve it with EDTA (we use 1/10 vol.
0.5 M EDTA) and desalt to taste. Some just spin the ppt out, but as you say
that may take some RNA with it.

Cheers,

-- 
| Dave Schweisguth                        For purposes of complying with    |
| dcs@proton.chem.yale.edu (MIME OK)      the New Jersey Right to Know Act: |
| http://proton.chem.yale.edu/~dcs/       Contents partially unknown.       |
| Yale Depts. of MB&B & Chemistry   Phone: 203-432-5208   Fax: 203-432-6144 |

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          Mon, 3 Apr 95 10:44:33 +0100
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To: Douglas J Bucklin <bucklin@selway.umt.edu>
From: etd@mole.bio.cam.ac.uk (Edwin ten Dam)
Subject: Re: transcription problem
Cc: rna@net.bio.net (rna)

Thus spoke the keyboard of Douglas J Bucklin (01*04*95):

 * Netters:
 *
 *       We are trying to synthesize several RNAs.  For most we have no
 problem,
 * but two of them are giving us problems.
 *       The two troublesome ones break down into one that works O.K.,
 * and another that is quite similar, but will not appear.  We transcribe
 * off of oligo templates with T7 RNA Pol. and use the protocol of
 * Milligan(sp?) et al. (NAR, late 80's) for the reactions.  Both RNAs are
 * designed to be stem and loop structures.  The sequences are virtually
 * identicle, the one that works does have five extra nucleotides at the
 * 3' end that are not involved in the stem loop.  All of the other bases,
 * for both RNAs, are in the stem loop.  The first three nucleotides
 * incorporated are G.
 *       We have tried templates that are ds only in the promoter region,
 * and fully ds templates.
 *         Do any of you have any ideas why two nearly identicle templates
 * would give these results?  Do you have suggestions to provide that may
 * aid in getting the troublesome template to produce?

I vaguely remember an article  (Milligan et al. (NAR, late 80's as well)
where the authors analyse the relative efficiency of templates and found
that U's in the first 8 nt's were counterproductive (they led to abortive
transcripts). Sorry, can't be more specific at the moment. Good luck, Edwin

Edwin ten Dam           etd@mole.bio.cam.ac.uk
Division of Virology - University of Cambridge
Tennis Court Road,  Cambridge   CB2 1QP,  U.K.
Phone: +44 1223 336918  - Fax: +44 1223 336926




From BIOSCI-REQUEST  Mon Apr  3 15:38:53 1995
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Date: Mon, 3 Apr 1995 14:40:33 -0500
To: bucklin@selway.umt.edu
From: jacek@lcbvax.cchem.berkeley.edu (Jacek Nowakowski)
Subject: Problems with transcription
Cc: rna@net.bio.net

        On 4/1/95 Douglas Bucklin wrote:

>       When doing the transcriptions there is often a heavy amount of
> insoluble goo that is produced.  We have found that the RNA is in that
> fraction.  Is that a common experience?  How do you redissolve that
> fraction?  Even after heating and diluting the scum still likes to persist.

        Dave Schweisguth replied on 4/2/95:

>That's magnesium pyrophosphate. Redissolve it with EDTA (we use 1/10 vol.
>0.5 M EDTA) and desalt to taste. Some just spin the ppt out, but as you say
>that may take some RNA with it.

        To prevent accumulation of the pyrophosphate during the
transcription reaction you may also add a small amount ( 1-4units/ml of
transcription) of yeast Inorganic Pyrophosphatase (ref. BioTechniques Vol.
9, No. 6 (1990) p.713)  It doesn't hurt anything, and it actually improves
the yield of transcription.  Definitely work up your reaction with EDTA
(see above).

        Jacek Nowakowski (Tinoco lab)





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From: dcs@proton.chem.yale.edu (Dave Schweisguth)
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Subject: Re: transcription II
To: rna@net.bio.net (RNA mailing list)
Date: Mon, 3 Apr 1995 20:38:53 -0400 (EDT)
In-Reply-To: <9504040005.AA07181@selway.umt.edu> from "Douglas J Bucklin" at Apr 3, 95 06:05:13 pm
Organization: Dept. of Chemistry, Yale University
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Douglas Bucklin quoth:
> 	I have played around with HPLC, but our coumn which was found 
> with the ancient artifacts of King Tut may have been a problem.  After 
> experimenting with the gradient for quite a long time I found a nice 
> step gradient with NaCl that seemed to separate several peaks nicely.  
> The peak that corresponded to my gel purified standard was well 
> isolated.  When I looked at the peak contents on a gel I still saw 
> abortive fragments.  The question:  What gradient system worked?

I use the DEAE column part of "A rapid method for purification of synthetic
oligoribonucleotides", BioTechniques 11(5):658-661, 1991. Briefly, that's 20
mM NaOAc, 6 M urea, 20% CH3CN, ph 6.5, 0-1.5M KCl over 50 minutes. Quite
reliable, if your HPLC is.

Cheers,

-- 
| Dave Schweisguth                        For purposes of complying with    |
| dcs@proton.chem.yale.edu (MIME OK)      the New Jersey Right to Know Act: |
| http://proton.chem.yale.edu/~dcs/       Contents partially unknown.       |
| Yale Depts. of MB&B & Chemistry   Phone: 203-432-5208   Fax: 203-432-6144 |

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Date: Tue, 18 Apr 1995 16:55:07 +0100
From: Bertrand Seraphin <Bertrand.Seraphin@embl-heidelberg.de>
Subject: Job
To: RNA@net.bio.net
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Funded research post-doctoral position available immediately=20
in the laboratory of B. Seraphin in the Gene Expression=20
Programme at EMBL Heidelberg, Germany to study RNA splicing=20
and processing in yeast as well as small nuclear=20
RiboNucleoProtein (snRNP) synthesis in yeast and mammalian=20
systems. Studies are focused on (but not limited to):
a) splice site selection and splicing catalysis;
b) intron recognition by the splicing machinery;
c) protein-RNA interactions and spliceosomal snRNP assembly,=20
particularly function of the Sm proteins;
d) structure-function of the RNase P and MRP=20
RiboNucleoProteins.

Recent publications include:
Seraphin, B. and S. Kandels-Lewis, 3=AB splice site=20
recognition in S. cerevisiae does not require base pairing=20
with U1 snRNA (1993). Cell, 73, 803-812;   Kandels-Lewis, S.=20
and B. Seraphin (1993), Role of U6 snRNA in 5' splice site=20
selection. Science, 262, 2035-2039;   Lygerou, Z., et al.=20
(1994), The POP1 gene encodes a protein component common to=20
the RNase MRP and RNase P ribonucleoproteins. Genes & Dev.,=20
8, 1423-1433;   Seraphin, B (1995). Sm and Sm-like proteins=20
belong to a large family: identification of proteins of the=20
U6 as well as the U1, U2, U4 and U5 snRNPs. EMBO J. in=20
press.

Additional projects in the eight other labs of the Gene=20
Expression Programme are targeted to the analysis of RNA=20
processing, transport and translation as well as=20
transcription. EMBL provides an exceptional scientific=20
environment with excellent facilities.

This position is funded for 12 month with possibilities of=20
extension. Interested candidates with general background in=20
molecular biology should send a C.V. to B. Seraphin by E-
mail (Seraphin@EMBL-Heidelberg.DE) or by mail to B.=20
Seraphin, EMBL, Meyerhofstrasse1, D-69117 Heidelberg,=20
Germany.


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                   NUCLEIC ACID AND PROTEIN SEQUENCE ANALYSIS
                       WORKSHOP FOR BIOMEDICAL RESEARCHERS
                              Pittsburgh, Pennsylvania
                              June 4-9, 1995



Pittsburgh Supercomputing Center (PSC) is again offering a five-day workshop on
"Nucleic Acid and Protein Sequence Analysis," June 4-9, 1995.  It is
funded by a grant from the National Center for Human Genome Research of
the National Institutes of Health.

The workshop will familiarize biomedical researchers
in applying supercomputing resources to
problems of concern in macromolecular sequence analysis.  Emphasis will be
on alignment of and pattern extraction from multiple sequences.
Participants will gain practical experience on PSC's Cray C-90 and T3D in
(1) comparing and aligning sequences, (2) identifying informative patterns
in a set of sequences; and (3) using extracted informative patterns to
identify related sequences.  Researchers will also learn several approaches
to database searching and  multiple sequence alignment, how to use profile
analysis effectively, and how to identify patterns in their sequences.
Participants are encouraged to bring sequence analysis problems from their
current research.  Extensive documentation will be given at the outset on
the PSC computing environment as well as on the specific programs
to be employed in the workshop.  No prior supercomputing experience is
required.

Workshop leaders are Dr. Gary Churchill, Cornell University, Dr. Michael
Gribskov, San Diego Supercomputing Center, and Dr. Hugh Nicholas, PSC.

A limited number of grants to cover travel and hotel accommodations are
available for U.S. academic participants.  ALL PARTICIPANTS ARE REQUIRED
TO PAY A $135 REGISTRATION FEE, IN ADVANCE, UPON ACCEPTANCE INTO THE WORKSHOP.

DEADLINE FOR SUBMITTING APPLICATIONS IS FRIDAY, APRIL 21, 1995.
Enrollment is lmited to 20 participants.

Additional information about this workshop can be found in
http://pscinfo.psc.edu/biomed/workshops95.html




                                      * * * * *



                     PITTSBURGH SUPERCOMPUTING CENTER
                     NUCLEIC ACID AND PROTEIN SEQUENCE ANALYSIS
                     WORKSHOP FOR BIOMEDICAL RESEARCHERS
                               June 4-9, 1995

                               APPLICATION


Name:          ________________________________________________________________

Affiliation:   ________________________________________________________________

Address:       ________________________________________________________________
               (Business)
               ________________________________________________________________

               ________________________________________________________________
               (Home)
               ________________________________________________________________

Telephone:  ____________________________         ______________________________
                   (Business)                                (Home)

*Social Security Number:  _______-_____-_______ Citizenship:___________________

Electronic Mail Address:_______________________________________________________

Status: ___Graduate  ___Post-doctoral Fellow  ___Faculty  ___Other (specify)

In order to attend the workshop, will you need funds for travel?___ lodging?___

Please indicate specifically any special housing, transportation or dietary
arrangements you will need: __________________________________________

How did you learn about this workshop:_________________________________________

REQUIREMENTS:

Applicants must submit a completed application form and a cover letter.  The
letter should describe, in one or two paragraphs, the sequence analysis
problems encountered in your research, and how participating in the workshop
will enhance this research.  Please include a brief statement describing your
level of experience with computers.  Faculty members, staff and post-docs
should provide a curriculum vita.  Graduate students must have a letter
of recommendation from a faculty member. If you have requested travel funds,
please include the cost of roundtrip air fare from your home to Pittsburgh and
indicate the amount of travel funds you will need. ALL PARTICIPANTS WILL BE
REQUIRED TO PAY A $135 ADVANCE REGISTRATION FEE UPON ACCEPTANCE INTO THE
WORKSHOP.

Please return all application materials by APRIL 21, 1995 to:



          Biomedical Workshop Applications Committee
          Pittsburgh Supercomputing Center
          4400 Fifth Avenue, Suite 230C
          Pittsburgh, PA 15213

Direct inquiries to: Nancy Blankenstein, blankens@psc.edu or 412/268-4960.

*Disclosure of Social Security Number is voluntary.

PSC does not discriminate on the basis of race, color, religion, sex, age,
creed, national or ethnic origin, or handicap.


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    <outnews+netnews.news.announce.conferences@andrew.cmu.edu>
Subject: CCL:Methods of Molecular Mechanics and Dynamics of Biopolymers workshop
Cc: Outbound News <outnews+netnews.bionet.announce@andrew.cmu.edu>,
        Outbound News <outnews+netnews.sci.research@andrew.cmu.edu>,
        Outbound News
    <outnews+netnews.sci.techniques.mag-resonance@andrew.cmu.edu>,
        Outbound News
    <outnews+netnews.bionet.molec-model@andrew.cmu.edu>,
        Outbound News
    <outnews+netnews.bionet.molbio.proteins@andrew.cmu.edu>,
        Outbound News <outnews+netnews.bionet.cellbiol@andrew.cmu.edu>,
        Outbound News <outnews+netnews.sci.research@andrew.cmu.edu>,
        Outbound News
    <outnews+netnews.sci.techniques.spectroscopy@andrew.cmu.edu>,
        Outbound News
    <outnews+netnews.sci.bio.technology@andrew.cmu.edu>,
        rna@net.bio.net, chemistry@osc.edu

"METHODS OF MOLECULAR MECHANICS AND DYNAMICS OF BIOPOLYMERS" WORKSHOP
                    Pittsburgh Supercomputing Center
                           August 16-19, 1995


The Pittsburgh Supercomputing Center (PSC) is hosting a workshop
on "Methods of Molecular Mechanics and Dynamics of Biopolymers,"
August 16-19, 1995.
The workshop will familiarize biomedical researchers with
computational methods and provide practice
in applying supercomputing resources to problems of concern in molecular
mechanics.  Practical experience on our supercomputers will be gained in
the application to:
(1) the theory and practice of molecular mechanics and dynamics;
(2) the development and refinement of molecular mechanics force fields;
(3) the problem of conformation mapping and analysis of polypeptide
structures, including the refinement of structure from measured NMR data;
and
(4) computation of interaction energies and free energies for protein-drug
interactions and conformational thermodynamics.

Workshop leaders are
Dr. Charles L. Brooks III, The Scripps Research Institute
and
Dr. Alexander D. MacKerell Jr., University of Maryland at Baltimore.

The worskhop will consist of lectures and extensive hands-on sessions.
General aspects of molecular mechanics software will be discussed and
a number of packages are available for use at the PSC.  However,
the programs CHARMM and QUANTA will be utilized most extensively in
demonstrations.  Hands-on sessions will be emphasized.
Participants will be able to work on the examples provided or
on their own experimental data.
No prior supercomputing experience is necessary.

This workshop is funded by a grant from the Biomedical Research Technology
Program, National Center for Research Resources, National Institutes of
Health.  TRAVEL, MEALS AND HOTEL ACCOMMODATIONS FOR RESEARCHERS AFFILIATED
WITH U.S. ACADEMIC INSTITUTIONS ARE SUPPORTED BY THIS GRANT.
Enrollment is limited to 20.  An application form is included.
Deadline for applications is: June 22, 1995.
Please direct inquires or send the following application form to
blankens@psc.edu.

Additional information about this workshop can be found in
http://pscinfo.psc.edu/biomed/workshops95.html



                         PITTSBURGH SUPERCOMPUTING CENTER
                         BIOMEDICAL  INITIATIVE
                         **************************************
                         August 16-19, 1995

                         APPLICATION


Name:________________________________________________________________________

Affiliation:_________________________________________________________________

Address:_____________________________________________________________________
                                  (Business)
_____________________________________________________________________________

____________________________________________________________________________
                                    (Home)
____________________________________________________________________________

Telephone:  ____________________              ______________________
                (Business)                            (Home)

*Social Security Number:  _______-_____-_______    Citizenship: ____________

Electronic Mail Address:____________________________________________________

Status: ___Graduate  ___Post-doctoral Fellow  ___Faculty  ___Other (specify)

Please indicate specifically any special housing, transportation or dietary
arrangements you will need:  _______________________________________________

How did you learn about this workshop? _____________________________________


REQUIREMENTS:

Applicants must submit a completed application form and a cover letter. The
letter should describe, in one or two paragraphs, your current research and
how participating in the workshop will enhance this research.  Please
include a brief statement describing your level of experience with computers.
Faculty members, staff and post-docs should provide a curriculum vita.
Graduate students must have a letter of recommendation from a faculty member.

Please return all application materials by June 22, 1995 to:

          Biomedical Workshop Applications Committee
          Pittsburgh Supercomputing Center
          4400 Fifth Avenue, Suite 230C
          Pittsburgh, PA 15213

Direct inquiries to: Nancy Blankenstein, blankens@psc.edu or 412/268-4960.

*Disclosure of Social Security Number is voluntary.

PSC does not discriminate on the basis of race, color, religion, sex, age,
creed, national or ethnic origin, or handicap.



From BIOSCI-REQUEST  Wed Apr 19 13:55:07 1995
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Message-ID: <8jZLUIi00WB88DHVkO@andrew.cmu.edu>
Date: Wed, 19 Apr 1995 16:52:36 -0400 (EDT)
From: "Alexander J. Ropelewski" <ar1z+@andrew.cmu.edu>
To: Outbound News
    <outnews+netnews.news.announce.conferences@andrew.cmu.edu>
Subject: CCL:STRUCTURE DETERMINATION FROM NMR
Cc: Outbound News <outnews+netnews.bionet.announce@andrew.cmu.edu>,
        Outbound News <outnews+netnews.sci.research@andrew.cmu.edu>,
        Outbound News
    <outnews+netnews.sci.techniques.mag-resonance@andrew.cmu.edu>,
        Outbound News
    <outnews+netnews.bionet.molec-model@andrew.cmu.edu>,
        Outbound News
    <outnews+netnews.bionet.molbio.proteins@andrew.cmu.edu>,
        Outbound News <outnews+netnews.bionet.cellbiol@andrew.cmu.edu>,
        Outbound News <outnews+netnews.sci.research@andrew.cmu.edu>,
        Outbound News
    <outnews+netnews.sci.techniques.spectroscopy@andrew.cmu.edu>,
        Outbound News
    <outnews+netnews.sci.bio.technology@andrew.cmu.edu>,
        rna@net.bio.net, chemistry@osc.edu,
        Outbound News
    <outnews+netnews.bionet.structural-nmr@andrew.cmu.edu>,
        str-nmr@net.bio.net, bruker-users-mail@bloch.cchem.berkeley.edu,
        ammrl-request@bloch.cchem.berkeley.edu

                    STRUCTURE DETERMINATION FROM NMR
                    Pittsburgh Supercomputing Center
                    June 25-28, 1995


Pittsburgh Supercomputing Center (PSC) is offering biomedical researchers a
"Structure Determination From NMR" Workshop.  The objective is to introduce
participants to the different techniques for the elucidation of solution
structures of biological macromolecules from nuclear magnetic resonance data.
The workshop is free to academic participants.


The worskhop will consist of lectures and extensive hands-on sessions.
The programs AMBER, Mardigras and MidasPlus will be discussed.  Hands-on
sessions will be emphasized.
Participants will be able to work on the examples
provided or on their own experimental data.
No prior supercomputing experience is necessary.

Workshop leaders are: Dr. David Case, The Scripps Research Institute; and
Drs Thomas James, Julie Newdoll and Uli Schmitz,
University of California, San Francisco.

This workshop is funded by a grant from the Biomedical Research Technology
Program, National Center for Research Resources, National Institutes of
Health. TRAVEL, MEALS AND HOTEL ACCOMMODATIONS FOR RESEARCHERS AFFILIATED
WITH U.S. ACADEMIC INSTITUTIONS ARE SUPPORTED BY THIS GRANT.
Enrollment is limited to 20.  An application form is included.
Deadline for applications is April 28, 1995.

Additional information about this workshop can be found in
http://pscinfo.psc.edu/biomed/workshops95.html




                             * * * * * * * * * *



                             PITTSBURGH SUPERCOMPUTING CENTER
                             BIOMEDICAL  INITIATIVE
                             STRUCTURE DETERMINATION FROM NMR
                             June 25-28, 1995

                             APPLICATION


Name:________________________________________________________________________

Affiliation:_________________________________________________________________

Address:_____________________________________________________________________
                                  (Business)
_____________________________________________________________________________

____________________________________________________________________________
                                    (Home)
____________________________________________________________________________

Telephone:  ____________________              ______________________
                (Business)                            (Home)

*Social Security Number:  _______-_____-_______    Citizenship: ____________

Electronic Mail Address:____________________________________________________

Status: ___Graduate  ___Post-doctoral Fellow  ___Faculty  ___Other (specify)

Please indicate specifically any special housing, transportation or dietary
arrangements you will need:  _______________________________________________

How did you learn about this workshop? _____________________________________


REQUIREMENTS:

Applicants must submit a completed application form and a cover letter. The
letter should describe, in one or two paragraphs, your current research and
how participating in the workshop will enhance this research.  Please
include a brief statement describing your level of experience with computers.
Faculty members, staff and post-docs should provide a curriculum vita.
Graduate students must have a letter of recommendation from a faculty member.

Please return all application materials by APRIL 28, 1995 to:

          Biomedical Workshop Applications Committee
          Pittsburgh Supercomputing Center
          4400 Fifth Avenue, Suite 230C
          Pittsburgh, PA 15213

Direct inquiries to: Nancy Blankenstein, blankens@psc.edu or 412/268-4960.

*Disclosure of Social Security Number is voluntary.

PSC does not discriminate on the basis of race, color, religion, sex, age,
creed, national or ethnic origin, or handicap.


From BIOSCI-REQUEST  Wed Apr 19 23:54:19 1995
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Received: by degas.imb-jena.de (950221.405.SGI.8.6.10/920502.SGI)
	for rna@net.bio.net id JAA02770; Thu, 20 Apr 1995 09:00:07 +0200
Date: Thu, 20 Apr 1995 09:00:07 +0200
From: jsuehnel@imb-jena.de (Juergen Suehnel)
Message-Id: <199504200700.JAA02770@degas.imb-jena.de>
To: rna@net.bio.net
Subject:  RNA on the World-Wide Web

RNA on the World-Wide Web
#########################


I would like to inform the RNA community that we
have recently set up two RNA related world-wide web (www) resources.


==============================================================
The first one (The RNA World) is a home page which tries to 
collect all RNA related www links.

Currently, it contains the following entries:


The RNA World
-------------------------------------------------------------------
   Image Library of Biological Macromolecules (IMB Jena)
   (with images of all RNA structures from the Protein Data Bank and Nucleic
   Acid Database) 

   Protein Data Bank (Brookhaven) (including RNA structures)[Gopher Link] 

   Protein Data Bank (Brookhaven) (including RNA structures)[WWW Link] 

   The Nucleic Acid Database (Rutgers) 

   RNA Secondary Structures (Boulder, CO) 

   BERLIN - RNA Databank of 5S rRNA and 5S rRNA Gene Sequences
   (CAOS/CAMM, The Netherlands) 

   rRNA - Database of Ribosomal Subunit Sequences (University of Antwerp,
   Belgium) 

   Ribosomal Database Project (Urbana, IL) 

   The Ribonuclease P Database (Indiana University, North Carolina State
   University) 

      Introduction 

      Archive 

   Compilation of tRNA and tRNA Gene Sequences (EMBL) 

   Small RNA Compilation (EMBL) (1991 !!!) 

   RNA Folding Software Guide (University of California, Irvine) 
--------------------------------------------------------------------

Its address is:   http://www.imb-jena.de/RNA.html .

If somebody knows of more RNA resources accessible via the 
world-wide web I would be grateful to get informed.

===================================================================

The second resource is the 

IMAGE LIBRARY OF BIOLOGICAL MACROMOLECULES

(http://www.imb-jena.de/IMAGE.html).

Currently, it contains images of all RNA structures available in
the Protein Data Bank or the Nucleic Acid Database
(about 60 structures), of about 120 proteins and 60 DNA structures.

Each structure is described in a short annotation file with 
bibliographic and sequence information.

The image files include a color coded distance plot and
various structure images (almost all of them also in stereo).
Currently, the total number of RNA image files is about 550 
(for the complete LIBRARY 2200).
Contrary, to the images provided by the Protein Data Bank or
US R Molecules (NIH) and like Swiss-3D-Image (University of
Geneva) our IMAGE LIBRARY contains non-standard images 
(different rendering techniques,labeling, color coding, 
different views ...). Further, images of buidling blocks,
like amino acids, standard and modified nucleotides, base pairs,
are also available.

There are many published structures
obtained by modeling procedures which probably never will be
included into the Protein Data Bank or Nucleic Acid Database.
It would be very useful if these structures were available via the 
IMAGE LIBRARY OF BIOLOGICAL MACROMOLECULES. 
If authors are interested to provide their structures to this 
LIBRARY they should contact me. 

======================================================================

Juergen Suehnel				  E-mail: jsuehnel@imb-jena.de	       
Biocomputing                              URL:	  http://www.imb-jena.de     
Institut fuer  Molekulare Biotechnologie  Tel.:	  +49 (0)3641 65 6200       
Beutenbergstr. 11, Postfach 100813        Fax :	  +49 (0)3641 65 6210       
D-07708 Jena / Germany                                           

From BIOSCI-REQUEST  Fri Apr 21 16:42:53 1995
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From: schmitz@picasso.ucsf.edu
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	id QAA04297; Fri, 21 Apr 1995 16:42:41 -0700
Date: Fri, 21 Apr 1995 16:42:41 -0700
Message-Id: <199504212342.QAA04297@dali.ucsf.edu>
To: rna@net.bio.net
Subject: RNA in the Analytical Centrifuge

Dear RNA-people,

I am trying to determine the molecular weights of several medium RNA species (15 to 40KD) by analytical ultracentrifugation.

Can somebody help me out with an approximate value for the partial molar volume for RNA or point out where experimental values of this kind have been published.

Thanks a lot,

Uli Schmitz

><><><><><><><><><><><><><><><><><><>
Uli Schmitz, Ph. D.
UC San Francisco
Dept. Pharmaceutical Chemistry
San Francisco, CA 94143-0446

Phone   (415) 476 4378;
Fax     (415) 476 0688;
schmitz@picasso.ucsf.edu
URL http://picasso.ucsf.edu/~schmitz
><><><><><><><><><><><><><><><><><><>


From BIOSCI-REQUEST  Sun Apr 23 10:16:38 1995
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From: santosh@physics.iisc.ernet.in
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Date: Wed, 24 May 95 22:24 GMT
To: rna@net.bio.net
Subject: help



From BIOSCI-REQUEST  Sun Apr 23 11:00:03 1995
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Date: Sun, 23 Apr 1995 13:59:07 -0400
From: francis@borduas.nlm.nih.gov (Francis Ouellette)
Message-Id: <9504231759.AA15230@borduas.nlm.nih.gov>
To: yac@net.bio.net, rna@net.bio.net, santosh@physics.iisc.ernet.in
Subject: Re: help
Reply-To: francis@ncbi.nlm.nih.gov
X-Sun-Charset: US-ASCII
Content-Length: 1833


> From BIOSCI-REQUEST@net.bio.net Sun Apr 23 13:18 EDT 1995
> From: santosh@physics.iisc.ernet.in
> Date: Wed, 24 May 95 22:24 GMT
> To: yac@net.bio.net
> Subject: help


The address for getting help is not that of the newsgroup, but what I
show below.  When you write to the newsgroup, two things happen:

1) everybody who subscribes to the newsgroup sees your message.
2) you do not get the help documentation

two things you don't want!

all the best,

francis 

--
| B.F. Francis Ouellette  
|
| francis@ncbi.nlm.nih.gov   



================================================================

Help messages may be obtained from the BIOSCI E-mail server
by sending one of these messages shown bellow to:

biosci-server@net.bio.net



info faq

	This will get you the latest FAQ for all the
	BIOSCI/bionet newsgroups.

info usinfo

	This will get you the latest information sheet for 
	subscription from the Americas and Pacific rim
	countries.

info ukinfo

	This will get you the latest information sheet for 
	subscription from Europe, Africa and central Asian 
	countries.


These message will return you the BIOSCI FAQ, and information on how
to subscribe to other newsgroups from the US and UK sites
(respectivly).

These documents are also available via gopher: 

gopher net.bio.net

 -->  6.  FAQs and Other Documents/

  -->  1.  BIOSCI Frequently Asked Questions.  
       2.  BIOSCI Access for users in the Americas and the Pacific Rim.
       3.  BIOSCI Access for users in Europe, Middle East and Africa.  
       4.  General Internet Information.  
       5.  Information on USENET (1 of 2).  
       6.  Information on USENET (2 of 2).  
       7.  bionet-checkgroups-msg  [ 3Jan95, 7kb].  

and World Wide Web:

http://www.net.bio.net/

=========================================================================




From BIOSCI-REQUEST  Sun Apr 23 11:36:02 1995
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          id AA16271; Fri, 21 Apr 1995 15:50:02 +0200
Date: Fri, 21 Apr 1995 15:50:01 +0200 (DFT)
From: Ole Matzura <ole@mango.mef.ki.se>
Subject: RNAdraw 1.0 beta now available!
To: Rnadraw Update List <bionet-software@cs.utexas.edu>,
        Rnadraw Info list <ae@dna.bio.warwick.ac.uk>,
        aflaloc@bgumail.bgu.ac.il, Anders.Wennborg@mtc.ki.se, art@aars.mit.edu,
        c-medina@cs.uiuc.edu, ebayna@ucsd.edu, ed@molbiol.uct.ac.za,
        ep@info.ucl.ac.be, escriou@pasteur.fr, Giuliano@ib.pi.cnr.it,
        nxp3@ciddpd2.em.cdc.gov, OTELLO@sc2a.unige.ch, pp001356@interramp.com,
        shjang@biho.taegu.ac.kr, tmargus@ebc.ee, tracy@svm.vetmed.wisc.edu
Message-Id: <Pine.3.89.9504211528.B23885-0100000@mango.mef.ki.se>
Mime-Version: 1.0
Content-Type: TEXT/PLAIN; charset=US-ASCII
Content-Length: 1917
Sender: tmargus@ebc.ee

Hello there!

RNAdraw is a complete RNA secondary structure/Basepair probability 
matrix / Heat curve calculation package for 32-bit MS-Windows. It offers 
an extensive easy-to-use (once you get the hang of it) interface and 
powerful editing/printing/calculation/analysis functions. Algorithms are 
based on the work of M. Zuker and J. McCaskill and were ported directly 
from the Vienna RNA package.

RNAdraw version 1.0 beta is now available for testing and using.
This version includes the following features over version 0.99-08:

1) Possibility to edit/modify/save/load all energy parameters used by 
the programs RNA calculational algorithms.

2) Possibility to export all RNA secondary structure / Basepair 
probability matrix / Probability histogram / Heat curve windows as 
Windows standard/placeable/enhanced metafiles. This gives a high quality
possibility to import views into major word-processing/layout/DTP 
applications.

3) Possibility to calculate basepair probability matrixes for imported 
structures. 

4) Lots of minor changes and new functions.

5) Extended help files.

6) etc...

So why wait? RNAdraw is available either via the RNAdraw WWW homepage 
located at : 
   
   http://broccoli.mfn.ki.se/rnadraw/rnadraw.html 

or via anonymous ftp at:

   broccoli.mfn.ki.se - in the pub/rnadraw directory. 

If you want direct info on updates and the RNAdraw add yourself to the 
RNAdraw mail list by sending you E-mail to the below address.

PLEASE notify me if you have any problems or suggestions concerning 
RNAdraw, I really want it to be as good as possible.

Good Luck!

Ole Matzura

------------------------------------------------------------
Ole Matzura                              ole@mango.mef.ki.se
Dept. of Medical Physics                 
Karolinska Inst. 
Stockholm, Sweden                           FAX:+46-8-326505
------------------------------------------------------------



