From owner-repertoires@net.bio.net Sun Jun 02 23:00:00 1996
Path: biosci!bcm.tmc.edu!cs.utexas.edu!chi-news.cic.net!news.compuserve.com!news.production.compuserve.com!news
From: Survey Administration <74750.1341@CompuServe.COM>
Newsgroups: bionet.molec-model,bionet.molecules.peptides,bionet.molecules.repertoires,bionet.parasitology
Subject: WE NEED YOUR INPUT
Date: 3 Jun 1996 03:21:35 GMT
Organization: Kitty Knight Corporation
Lines: 25
Message-ID: <4otlnv$3ni$8@mhade.production.compuserve.com>
Xref: biosci bionet.molec-model:951 bionet.molecules.peptides:333 bionet.molecules.repertoires:155 bionet.parasitology:1589

Please excuse this brief intrusion, but we are trying to locate 
any and all holders of academic degrees conferred within the last 
ten (10) years.

The Kitty Knight Corporation, Boston, MA, is currently searching 
for qualified individuals to participate in a ***PAID*** study 
focusing on post-secondary, graduate, and professional education 
in the United States.

Holders of ALL types of degrees in ALL fields of study are needed. 
 We would like to hear from you as long as your degree was earned 
at an accredited institution in the United States.

After an initial screening, qualified participant will be asked to 
complete a questionaire of approx 150 questions.  Everyone who 
completes the survey will receive a $100 stipend.  Naturally, 
*ALL* information will be held in the strictest confidence.  

To express interest, please send your name, mailing address, and 
photocopies of **ALL** degrees you have earned to:  The Kitty 
Knight Corporation, Attn: Study 96-3H, Back Bay Annex, P O Box 
546, Boston, MA  02117.  (If not obvious from the degree, please 
indicate the field of study.)

Thank You Very Much!

From owner-repertoires@net.bio.net Tue Jun 04 23:00:00 1996
Path: biosci!daresbury!yama.mcc.ac.uk!zippy.dct.ac.uk!str-ccsun!strath-cs!queens-belfast.ac.uk!queens-belfast.ac.uk!nntp
Newsgroups: bionet.molecules.repertoires
Subject: Upcoming FAQ for molreps
Message-ID: <1996Jun5.115805.6559@queens-belfast.ac.uk>
From: "N.V.McFerran" <n.mcferran@qub.ac.uk>
Date: 5 Jun 96 11:58:02 GMT
Nntp-Posting-Host: 104_mbc.bc.qub.ac.uk
Lines: 5

Following Tom's suggestion I will soon be posting a monthly FAQ
to the molreps newsgroup so watch this space...

Andrew
a.wallace@queens-belfast.ac.uk

From owner-repertoires@net.bio.net Wed Jun 05 23:00:00 1996
Path: biosci!ihnp4.ucsd.edu!munnari.OZ.AU!news.mel.connect.com.au!harbinger.cc.monash.edu.au!lugb.latrobe.edu.au!newsmgr
From: Mick Foley <m.foley@latrobe.edu.au>
Newsgroups: bionet.molecules.repertoires
Subject: (no subject)
Date: 6 Jun 1996 00:10:39 GMT
Organization: LaTrobe University
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Hi all,

I may have asked this of the group before, but does anyone have or know 
where I can get primers to make a scFv library from either hybdridomas or 
spleens from rats. Is there the same info on the rat repertoire anywhere. 
Sorry if this is a repeat, and thanks in advance for any help 
(primers to make rat Fabs would also be useful).

Cheers

Mick




From owner-repertoires@net.bio.net Thu Jun 06 23:00:00 1996
Path: biosci!daresbury!not-for-mail
From: "Engle" <engle@macnet.vpharm.com>
Newsgroups: bionet.molecules.repertoires
Subject: Employment Opportunity-Diversity Chem
Date: 7 Jun 1996 15:24:49 +0100
Lines: 25
Sender: lpddist@mserv1.dl.ac.uk
Distribution: bionet
Message-ID: <4p9e3h$p0a@mserv1.dl.ac.uk>
Original-To: "Molecular Repertoires" <molreps@dl.ac.uk>

Combinatorial Chemists

Vertex Pharmaceutical's expanding combinatorial chemistry group has immediate
openings available for associate level chemists.  Applicants must have a
strong background in synthetic organic chemistry with a minimum of two years
of post-bachelor degree, full time bench laboratory experience and hands-on
familiarity with programmable laboratory equipment.  Specific experience with
solid-supported small molecule organic synthesis and/or laboratory automation
equipment is a significant plus.

Vertex offers a highly interactive, multidisciplinary approach with some of
the best researchers in the industry.  Our strong computational chemistry and
informatics groups, analytical sciences, and established leadership in
structure-based drug design form an exciting environment in which to
integrate the tools of automated organic synthesis with the process of
pharmaceutical research.  Resumes may be forwarded to:  Vertex
Pharmaceuticals Incorporated, Recruiting Manager, Code "netchem", 130 Waverly
Street, Cambridge, MA  02139-4242; FAX: (617) 577-6645; or email to:
recruiting@vpharm.com 

We are an Equal Opportunity Employer

Please visit our homepage at http://www.vpharm.com. 



From owner-repertoires@net.bio.net Mon Jun 10 23:00:00 1996
Path: biosci!NMSU.EDU!dkim
From: dkim@NMSU.EDU ("D. KIM")
Newsgroups: bionet.molecules.repertoires
Subject: "Biopanning" on a membrane
Date: 11 Jun 1996 09:46:36 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 12
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <Pine.SUN.3.91.960611104047.9585A-100000@verdi>
NNTP-Posting-Host: net.bio.net

Hello

I was wondering if there was a specific reason why affinity selection 
(biopanning) is often done using a polystyrene well (e.g. a Petri dish or 
a 96-well immunoassay plate).

Why is biopanning not done by binding the ligand onto a membrane such as 
PVDF or nitrocellulose, followed by blocking and affinity selection?  Is 
a polystyrene well/dish better suited for some reason?

Daniel Kim
dkim@nmsu.edu

From owner-repertoires@net.bio.net Mon Jun 10 23:00:00 1996
Path: biosci!daresbury!yama.mcc.ac.uk!zippy.dct.ac.uk!str-ccsun!strath-cs!queens-belfast.ac.uk!bcg0197
Newsgroups: bionet.molecules.repertoires
Subject: Re: (no subject) - rat primers
Message-ID: <1996Jun11.102107.6617@queens-belfast.ac.uk>
From: bcg0197@queens-belfast.ac.uk (a.wallace@queens-belfast.ac.uk)
Date: 11 Jun 96 10:21:07 GMT
References: <4p57lv$mc8@lugb.latrobe.edu.au>
Organization: Queen's University of Belfast
Lines: 28

In article <4p57lv$mc8@lugb.latrobe.edu.au>, Mick Foley <m.foley@latrobe.edu.au> writes:
> Hi all,
> 
> I may have asked this of the group before, but does anyone have or know 
> where I can get primers to make a scFv library from either hybdridomas or 
> spleens from rats. Is there the same info on the rat repertoire anywhere. 
> Sorry if this is a repeat, and thanks in advance for any help 
> (primers to make rat Fabs would also be useful).
> 
> Cheers
> 
> Mick
> 
> 
> 
      I suppose you could try asking Greg Winter (I think his
      address is gw@mrc-lmb.cam.ac.uk) but he may only have the
      primers for mouse (as would most people, I suspect).

      Andrew
-- 
      ================================================================
      Andrew Wallace, Ph.D.
      School of Biology and Biochemistry
      The Queen's University of Belfast           Tel. +44-1232-335786
      97 Lisburn Road                             Fax  +44-1232-236505
      Belfast BT9 7BL                   a.wallace@queens-belfast.ac.uk
      Northern Ireland (UK)  http://www.qub.ac.uk/b&bchem/rbiochem.htm

From owner-repertoires@net.bio.net Tue Jun 11 23:00:00 1996
Path: biosci!daresbury!yama.mcc.ac.uk!news.salford.ac.uk!aber!bath.ac.uk!dcl-cs!strath-cs!queens-belfast.ac.uk!queens-belfast.ac.uk!nntp
Newsgroups: bionet.molecules.repertoires
Subject: New epitope tag
Message-ID: <1996Jun12.105059.6626@queens-belfast.ac.uk>
From: Andrew Wallace <a.wallace@qub.ac.uk>
Date: 12 Jun 96 10:50:59 GMT
Nntp-Posting-Host: 104_mbc.bc.qub.ac.uk
Lines: 10

A while ago, Andrew Bradbury asked about novel epitope tags.
I have seen one in a recent issue of Gene which may be useful.
It is derived from the VP7 major core protein of bluetongue virus
and the sequence is QYPALT in single-letter code. The authors call
it BTag.

Reference: Wang, L-F. et al., Gene 169 (1996) 53-58.

Andrew
a.wallace@queens-belfast.ac.uk

From owner-repertoires@net.bio.net Tue Jun 11 23:00:00 1996
Path: biosci!daresbury!yama.mcc.ac.uk!news.salford.ac.uk!aber!bath.ac.uk!dcl-cs!strath-cs!queens-belfast.ac.uk!queens-belfast.ac.uk!nntp
Newsgroups: bionet.molecules.repertoires
Subject: Braunschweig meeting
Message-ID: <1996Jun12.114923.6629@queens-belfast.ac.uk>
From: Andrew Wallace <a.wallace@qub.ac.uk>
Date: 12 Jun 96 11:49:22 GMT
Nntp-Posting-Host: 104_mbc.bc.qub.ac.uk
Lines: 7

Could someone who has a copy of the Braunschweig libraries meeting
in electronic form please post it here?

Thanks,

Andrew
<a.wallace@queens-belfast.ac.uk>

From owner-repertoires@net.bio.net Tue Jun 11 23:00:00 1996
Path: biosci!daresbury!yama.mcc.ac.uk!news.salford.ac.uk!aber!bath.ac.uk!dcl-cs!strath-cs!queens-belfast.ac.uk!bcg0197
From: bcg0197@queens-belfast.ac.uk (a.wallace@queens-belfast.ac.uk)
Newsgroups: bionet.molecules.repertoires
Subject: Molreps FAQ for June 1996
Message-ID: <1996Jun12.113406.6627@queens-belfast.ac.uk>
Date: 12 Jun 96 11:34:06 GMT
Organization: Queen's University of Belfast
Lines: 134

      Here is this month's edition (the first) of the molreps FAQ.

      You are all hereby cordially invited to send me corrections,
      particularly if something is not true or outdated, comments,
      flames (but not too many I hope), etc.

      Any additional information or questions you would like to see
      included are especially welcome.

      My thanks to Franco Felici and Tom Schneider for their
      help in preparing this first version.

      ===================================================================
      M O L R E P S   F R E Q U E N T L Y   A S K E D   Q U E S T I O N S
      *************   *******************   *********   *****************

      **1 Where can I obtain libraries?**

      1.1 _Phage Libraries_
      	 You can try approaching the following people and
           organisations:

      1.1.1 pIII/6-mer, pIII/15-mer, pVIII-4/15-mer libraries
         	  George Smith, University of Missouri, FAX +1-573-882-0123

      1.1.2 pVIII/9-mer, pVIII/9-merCys and pVIII/zinc-finger
             phagemid libraries
            Alessandra Luzzago, IRBM P. Angeletti, luzzago@irbm.it
            Franco Felici, IRBM P. Angeletti, felici@irbm.it
            (NON-COMMERCIAL USERS ONLY)

      1.1.3 Antibody scFvs with synthetic CDRs
      	  Greg Winter, MRC-LMB Cambridge, gw@mrc-lmb.cam.ac.uk
      	  (NON-COMMERCIAL USERS ONLY)

      1.1.4 Commercial Sources
      	  Stratagene (Fab fragments in phage lambda)
      	  Affymax
      	  Pharmacia
      	  Cambridge Antibody Technology

      1.2 _Synthetic Peptide Libraries_

      1.2.1 Commercial Sources
      	  Affymax
      	  Selectide
      	  Chiron Corporation
      	  Most of the major peptide companies will
      	   custom-synthesise a library to your requirements.

      1.3 _Nucleic Acid Libraries_ (Aptamers)

      1.3.1 Jack Szostak at Harvard medical school?
      1.3.2 NEXUS corporation (Larry Gold)?


      1.4 _Organic Chemical Libraries_

      1.4.1 Affymax?
      1.4.2 Parke-Davis (DIVERSOMERS)?



      **2) Where can I get anti-phage antibodies?**

      2.1 anti-pIII MAb from Michael Tesar
      	mte@venus.gbf-braunschweig.d400.de

      2.2 anti-pIII polyclonals from GATC, a German company,
      	FAX +49-7531-57313	TEL +49-7531-57204

      2.3 rabbit anti-M13 from Stratagene.



      **3) How can I make my own libraries?**

      3.1 _Phage Libraries_
           You can obtain suitable vectors and strains from most of 
           the sources in 1).
           For phagemid work you can get XL-1 Blue cells from
           Stratagene and M13K07 helper phage from Pharmacia.

      3.2 _Synthetic Peptide Libraries_

      3.2.1 Manual synthesis
      	  Houghten's "Tea Bag" method
      	  Geysen's "Pin" method
      	  Both of these can be adapted to produce either
      	  support-bound or soluble libraries.

      3.2.2 Automated synthesis
      	  Chiron Corporation (Zuckermann)
      	  Advanced Chemtech (Commercial robot for 75K sterling)


      3.3 _Nucleic Acid Libraries_

      3.3.1 PCR methods


      3.4 _Organic Chemical Libraries_

      3.4.1 Manual synthesis
      3.4.2 Automated synthesis (Advanced Chemtech)



      **4) How can I analyse the results of my selection?**

      4.1 Insert sequencing (phage libraries)

      4.2 Micropanning 
                (Smith and Scott, Methods Enzymol. (1993) 217:228-257)
      4.3 Dot-blotting
                (Felici et al., J. Mol. Biol. (1991) 222:301-310)
      4.4 ELISA 
                (Smith and Scott, Methods Enzymol. (1993) 217:228-257)
                (Dente et al. Gene (1994) 148:7-13)
      4.5 Colony immunoscreening 
                (Christian et al. J. Mol. Biol. (1992) 227, 711-718)
                (Felici et al. Gene (1993) 128, 21-27)
      4.5 Plaque immunoscreening
                (Luzzago et al., Gene (1993) 128:51-57)
                (Felici et al., Methods Enzymol. (1996) 267:116-129)

-- 
      ================================================================
      Andrew Wallace, Ph.D.
      School of Biology and Biochemistry
      The Queen's University of Belfast           Tel. +44-1232-335786
      97 Lisburn Road                             Fax  +44-1232-236505
      Belfast BT9 7BL                   a.wallace@queens-belfast.ac.uk
      Northern Ireland (UK)  http://www.qub.ac.uk/b&bchem/rbiochem.htm

From owner-repertoires@net.bio.net Thu Jun 13 23:00:00 1996
Path: biosci!rutgers!sgigate.sgi.com!news-res.gsl.net!news.gsl.net!nntp.coast.net!oleane!jussieu.fr!news.sri.ucl.ac.be!news.belnet.be!swsbe6.switch.ch!scsing.switch.ch!rzunews.unizh.ch!newsadm
From: simone@erdw.ethz.ch
Newsgroups: bionet.molecules.repertoires
Subject: Nissim scFv phage display library
Date: Fri, 14 Jun 1996 13:49:14 +0200
Organization: University of Zurich, Switzerland
Lines: 3
Message-ID: <31C151BA.7AAA@erdw.ethz.ch>
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Has anybody got any experience with the Nissim scFv library? So far we
have only heard of good results, but obviously it is usually more
difficult to find information of people who have had difficulties.

From owner-repertoires@net.bio.net Thu Jun 13 23:00:00 1996
Path: biosci!daresbury!not-for-mail
From: Andrew Wallace <A.Wallace@Queens-Belfast.AC.UK>
Newsgroups: bionet.molecules.repertoires
Subject: EMBO Course on phage display
Date: 14 Jun 1996 15:20:00 +0100
Lines: 243
Sender: lpddist@mserv1.dl.ac.uk
Distribution: bionet
Message-ID: <4prseg$cie@mserv1.dl.ac.uk>
Original-To: molreps@dl.ac.uk

This attachment is a binhex-encoded document containing the
      application for for Andrew Bradbury's phage display EMBO
      course in September.
Andrew
--============_-1377532728==_============
Content-Disposition: attachment; filename="applicants29=2=96.doc"
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!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!
!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!
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!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!
!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!
!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!
!!!!!!!!!!!!!0*m!!!:


--============_-1377532728==_============
Content-type: text/plain; charset="us-ascii"

Andrew Bradbury
SISSA c/o ICGEB
Area di Ricerca
Padriciano 99
Trieste 34012
Italy

Tel +39 40 398995
Fax +39 40 398991



--============_-1377532728==_============--

From owner-repertoires@net.bio.net Thu Jun 13 23:00:00 1996
Path: biosci!EMAIL.UNC.EDU!briankay
From: briankay@EMAIL.UNC.EDU (Brian Kay)
Newsgroups: bionet.molecules.repertoires
Subject: phage display manual
Date: 14 Jun 1996 06:22:12 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 36
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <v02140b00ade6dd14b03b@[152.2.66.22]>
NNTP-Posting-Host: net.bio.net

Hi All,

Jill Winter (Chiron), John McCafferty (CAT), and I are pleased to announce
that the book, "Phage display of peptides and proteins: a laboratory
manual", is in production at Academic Press. If you wish to peruse the
table of contents, I have created a webpage companion to the book. Its
address is

 http://www.unc.edu/depts/biology/phagedisplay.html

Only ~1/3 of the linked pages are complete.

The book will be a soft-cover manual, spiral bound, with ~330 pages. It
costs $39.95 and can be oredred by fax (1-800-874-6418) or telephone
(1-800-321-5068) from Academic Press. The ISDN is 0-12-402380-0.

Sincerely yours,


Brian

~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
Brian Kay
Associate Professor of Biology
321 Fordham Hall
University of North Carolina at Chapel Hill
Chapel Hill, NC 27599-3280

Office: 919-962-2144
Fax: 919-962-1625
Email: briankay@email.unc.edu
Webpage: http://www.unc.edu/depts/biology/kay.html
Phage Display Book: http://www.unc.edu/depts/biology/phagedisplay.html
~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~



From owner-repertoires@net.bio.net Sun Jun 16 23:00:00 1996
Path: biosci!daresbury!not-for-mail
From: Andrew Wallace <A.Wallace@Queens-Belfast.AC.UK>
Newsgroups: bionet.molecules.repertoires
Subject: Braunschweig Symposium
Date: 17 Jun 1996 11:49:22 +0100
Lines: 166
Sender: lpddist@mserv1.dl.ac.uk
Distribution: bionet
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Original-To: molreps@dl.ac.uk

For details about the Braunschweig Symposium, consult the URL
http://transfac.gbf-braunschweig.de/Symposien/Welcom2.html

Here is some of the information you will find there:


>                             GBF-SYMPOSIUM
> 
>                Antibody Technology and Applications in
>                         Health and Environment
> 
> 
>                         September 6 - 10, 1996
>                        in Braunschweig, Germany
> 
> Goals and Scope
> The goals of the Symposium are to present latest advances in the
field
> of antibody technology with regard to emerging innovative
approaches
> and applications in health and environment. During the first part
of
> the symposium research progress will be presented in the fields
of
> natural immune repertoires, antibody structure and function and
> recombinant antibody technology including human and humanized
> antibodies, phage display techniques, combinatorial libraries and
> bispecific or catalytic antibodies. In the second part,
potentials and
> problems of antibody expression in cell cultures, transgenic
animals
> and plants will be discussed with regard to the antibody
application
> sessions in the third part of the Symposium. The final sessions
will
> analyze the use of antibody for prophylaxis and therapy and in a
> variety of other fields with emphasis on the environment.
Interactions
> will be encouraged during round-table sessions where potential
uses,
> common difficulties and limitations of antibody technology will
be
> discussed. Additional time for discussions will be available
during
> poster sessions, social activities and informal periods of time
in the
> Hotel Mercure where most of the participants will be
accommodated.
> Younger scientiests will have the opportunity to submit abstracts
for
> short oral presentations of selected posters in the main
sessions.
>    
------------------------------------------------------------------------
> 
> 
> Main topics of the symposium and confirmed speakers:
> 
>                Antibodies: Natural Repertoires, Structure and
Function
>                          A. Coutinho (France), A. McPherson
(USA), A.
>                          Skerra (Germany)
> 
>                Antibody Engineering
>                          [Image]Display Technology
>                          A. Bradbury (Italy), A. Griffith (U.K.),
M.
>                          Little (Germany), P.-E. Nygren (Sweden),
>                          A. Pl|ckthun (Switzerland), G.P. Smith
(USA)
> 
>                          [Image]Combinatorial Libraries
>                          J. Collins (Germany), R. Cortese
(Italy), R.
>                          Sodoyer (France), A. Williamson (USA),
B. Kay
>                          (USA)
> 
>                          [Image]Human and Humanized Antibodies
>                          N. Lonberg (USA)
> 
>                          [Image]Bispecific and Catalytic
Antibodies
>                          P. Holliger (U.K.), G. Gallacher (U.K.),
P.
>                          Carter (USA)
> 
>                Expression of MAbs and Tag Systems
>                          B. Brizzard (USA), B. Haase (Germany),
A.
>                          Depicker (Belgium), H. Meade (USA), H.
Kvhler
>                          (USA)
> 
>                Medical Applications
>                          [Image]Diagnostic and Imaging
>                          A. Wu (USA), W. Wels (Germany); R.
Miller
>                          (USA)
> 
>                          [Image]Therapie and Prophylaxis
>                          M. Bendig (UK), G.S. Chhatwal (Germany),
S.J.
>                          Cryz (Switzerland),
>                          F. Emmrich (Germany), J. Engberg
(Denmark),
>                          H. Lindhofer (Germany), J.R. McGhee
(USA)
> 
>                Environmental Applications
>                          J. Kvhl (Germany), E. Conway de Macario
>                          (USA), M. Tesar (Germany), B. Harris
(UK)
>                          P.V. Choudary (USA)
> 
------------------------------------------------------------------------
> 
> 
> If you would like to receive more information, please submit the
fill
> out form:
> 
>  First Name
>  Last Name and Title
>  Organization
>  Department
>  Address
>  City
>  ZIP/Postal Code
>  State/Country
>  Telephone
>  Fax
>  E-Mail
> Comments
> 
> 
> 
> 
> 
> You could also reach us at the following address:
> You could also reach us at the following address:
>                                                           
[Greetings]
>           GBF-Braunschweig
>           Antibody Symposium
>           Department Microbiology/Cell Biology
>           Mascheroder Weg 1
>           D - 38124 Braunschweig
>           Germany
>           Tel: +49 531 6181 400 (H. Brink)
>           Fax: +49 531 6181 411
> 
> 
> or directly via E-Mail:
> [Image]Antibody Symposium at the GBF-Braunschweig [Image]
> 
>    
------------------------------------------------------------------------
> 
> 
> Organizers: Gusharan S. Chhatwal, Bernd Haase, Michael Tesar,
Carlos
> A. Guzman, Kenneth N. Timmis
> 


From owner-repertoires@net.bio.net Sun Jun 16 23:00:00 1996
Path: biosci!qub.ac.uk!a.wallace
From: a.wallace@qub.ac.uk (Andrew Wallace)
Newsgroups: bionet.molecules.repertoires
Subject: EMBO Course - Date Correction.
Date: 17 Jun 1996 04:39:17 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 11
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Message-ID: <199606171139.EAA09730@net.bio.net>
NNTP-Posting-Host: net.bio.net

Looks like I've got my dates wrong again - the phage display EMBO course 
is in November, not September as I said in my previous message on this 
topic.

Andrew

"Ohh Dearie Mee" as they say in "The High Life"
P.S. When is "The Comedy Zone" going to put on some new shows instead of 
repeats from 1990?



From owner-repertoires@net.bio.net Tue Jun 18 23:00:00 1996
Path: biosci!daresbury!not-for-mail
From: "Janet Clench, Library, Tel:(39 6)91093220" <CLENCH@irbm.it>
Newsgroups: bionet.molecules.repertoires
Subject: It's been a long time comin', but let's hope it's worth it ...
Date: 19 Jun 1996 11:38:06 +0100
Lines: 204
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*********************************************************
SUBJECT:	Combinatorial & Phage Libraries
DATE:	May 27, June 3,10,17, 1996
********************************************************

Biotechniques  20: 5 (MAY 1996)
P Reddy, K Mckenney
Improved method for the production of M13 phage 
and single-stranded DNA for DNA sequencing
854

Tetrahedron  52: 20 (MAY 13 1996)
E Leikauf, F Barnekow, H Koster
A combinatorial protecting group strategy for 
oligonucleotide synthesis
6913-6930

Tetrahedron  52: 20 (MAY 13 1996)
T Lescrinier, R Busson, J Rozenski, G Janssen, A 
Vanaerschot, P Herdewijn
Incorporation of 5-hydroxytryptophan in 
oligopeptides
6965-6972

Tetrahedron Letters  37: 19 (MAY 6 1996)
J Nielsen, PH Rasmussen
Implementation of a combinatorial cleavage and 
deprotection scheme .1. Synthesis of phthalhydrazide 
libraries.
3351-3354

Antimicrobial Agents and Chemotherapy  40: 5 (MAY 
1996)
SE Blondelle, E Perezpaya, RA Houghten
Synthetic combinatorial libraries: Novel discovery 
strategy for identification of antimicrobial agents
1067-1071

European Journal of Immunology  26: 3 (MAR 1996)
RMT Dewildt, R Finnern, WH Ouwehand, AD Griffiths, 
WJ Vanvenrooij, RMA Hoet
Characterization of human variable domain antibody 
fragments against the U1 RNA-associated A protein, 
selected from a synthetic and a patient-derived 
combinatorial V gene library
629-639

Molecular Biology  30: 1 Part 1 (JAN-FEB 1996)
AA Ilichev, NV Melamed, IA Razumov, AZ Maksyutov, 
AV Pereboev, AI Zakabunin, VB Loktev
Expression of gene fragments for the E2 protein of 
Venezuelan equine encephalomyelitis virus in a phage 
T7 RNA polymerase-based system
46-50

Proceedings of the National Academy of Sciences of 
the United States of America  93: 9 (APR 30 1996)
YM Zhao, TW Muir, SBH Kent, E Tischer, JM Scardina, 
BT Chait
Mapping protein-protein interactions by affinity-
directed mass spectrometry
4020-4024

Basic DNA and RNA Protocols (Series: Methods in 
Molecular Biology  58 (1996))
GZ Yu
Cloning into M13 bacteriophage vectors
343-348

Basic DNA and RNA Protocols (Series: Methods in 
Molecular Biology  58 (1996))
FM Tomley
M13 phage growth and single-stranded DNA 
preparation
359-362

Plant Cell  8: 4 (APR 1996)
MNV Williams, G Freshour, AG Darvill, P Albersheim, 
MG Hahn
An antibody Fab selected from a recombinant phage 
display library detects deesterified pectic 
polysaccharide Rhamnogalacturonan II in plant cells
673-685

Journal of Biological Chemistry  271: 18 (MAY 3 1996)
P Steinberger, D Kraft, R Valenta
Construction of a combinatorial IgE library from an 
allergic patient - Isolation and characterization of 
human IgE Fabs with specificity for the major timothy 
grass pollen allergen, Phl p 5
10967-10972

Clinical Immunology and Immunopathology  79: 2 
(MAY 1996)
M Sioud, O Forre, A Dybwad
Selection of ligands for polyclonal antibodies from 
random peptide libraries: Potential identification of 
(auto)antigens that may trigger B and T cell responses 
in autoimmune diseases
105-114

International Archives of Allergy and Immunology  
110: 1 (MAY 1996)
R Crameri, K Blaser
Cloning Aspergillus fumigatus allergens by the pJuFo 
filamentous phage display system
41-45

Journal of Immunology  156: 10 (MAY 15 1996)
M Eggena, SR Targan, L Iwanczyk, A Vidrich, LK 
Gordon, J Braun
Phage display cloning and characterization of an 
immunogenetic marker (perinuclear anti-neutrophil 
cytoplasmic antibody) in ulcerative colitis
4005-4011

Science  272: 5266 (MAY 31 1996)
RF Service
Chemistry - Combinatorial chemistry hits the drug 
market
1266-1268

Scientist  10: 10 (MAY 13 1996)
KS Brown
Drug, biotech firms beginning to embrace 
combinatorial chemistry
1

Journal of Medicinal Chemistry  39: 10 (MAY 10 1996)
JM Gao, XH Cheng, RD Chen, GB Sigal, JE Bruce, BL 
Schwartz, SA Hofstadler, GA Anderson, RD Smith, GM 
Whitesides
Screening derivatized peptide libraries for tight 
binding inhibitors to carbonic anhydrase II by 
electrospray ionization mass spectrometry
1949-1955

Journal of Immunology  156: 11 (JUN 1 1996)
C Prezzi, M Nuzzo, A Meola, P Delmastro, G Galfre, R 
Cortese, A Nicosia, P Monaci
Selection of antigenic and immunogenic mimics of 
hepatitis C virus using sera from patients
4504-4513

Nature Biotechnology  14: 3 (MAR 1996)
TJ Vaughan, AJ Williams, K Pritchard, JK Osbourn, AR 
Pope, JC Earnshaw, J Mccafferty, RA Hodits, J Wilton, 
KS Johnson
Human antibodies with sub-nanomolar affinities 
isolated from a large non-immunized phage display 
library
309-314

Nature Biotechnology  14: 3 (MAR 1996)
MA Alvarez, H Fu, C Khosla, DA Hopwood, JE Bailey
Engineered biosynthesis of novel polyketides: 
Properties of the whiE aromatase/cyclase
335-338

Nature Biotechnology  14: 4 (APR 1996)
AM Wu
In vivo veritas: Live phage display panning
429-431

Nature Biotechnology  14: 4 (APR 1996)
D Neri, H Petrul, G Winter, Y Light, R Marais, KE 
Britton, AM Creighton
Radioactive labeling of recombinant antibody 
fragments by phosphorylation using human casein 
kinase II and [gamma-P-32]-ATP
485-490

Nature Biotechnology  14: 4 (APR 1996)
DM Evans, KP Williams, B Mcguinness, G Tarr, F 
Regnier, N Afeyan, S Jindal
Affinity-based screening of combinatorial libraries 
using automated, serial-column chromatography
504-507

Journal of Molecular Biology  259: 1 (MAY 31 1996)
H Zhang, MM Skinner, WS Sandberg, AHJ Wang, TC 
Terwilliger
Context dependence of mutational effects in a protein: 
The crystal structures of the V351, 147V and 
V351/147V gene V protein core mutants
148-159

Journal of Molecular Biology  258: 5 (MAY 24 1996)
LLC Bonnycastle, JS Mehroke, M Rashed, X Gong, JK 
Scott
Probing the basis of antibody reactivity with a panel 
of constrained peptide libraries displayed by 
filamentous phage
747-762

Proceedings of the National Academy of Sciences of 
the United States of America  93: 10 (MAY 14 1996)
P Kast, M Asifullah, N Jiang, D Hilvert
Exploring the active site of chorismate mutase by 
combinatorial mutagenesis and selection: The 
importance of electrostatic catalysis
5043-5048



From owner-repertoires@net.bio.net Wed Jun 19 23:00:00 1996
Path: biosci!daresbury!not-for-mail
From: Franco Felici <FELICI@irbm.it>
Newsgroups: bionet.molecules.repertoires
Subject: Methods in Enzymology - Volume 267
Date: 20 Jun 1996 09:47:07 +0100
Lines: 134
Sender: lpddist@mserv1.dl.ac.uk
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Message-ID: <4qb36b$sdh@mserv1.dl.ac.uk>
Original-To: molreps@dl.ac.uk

Some of you may find the following book interesting...

All the best,

Franco

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

Methods in Enzymology

Volume 267

Combinatorial Chemistry

EDITED BY
John N. Abelson

ACADEMIC PRESS, 1996
San Diego New York Boston London Sydney Tokyo Toronto


Table of Contents
=================


          Section I. Phage Display Libraries

1. Affinity Maturation of Phage-Displayed Peptide Ligands
                                        by J. YU and G.P. SMITH

2. Selection for Protease Inhibitors Using Bacteriophage Display
                                        by W. MARKLAND et al.

3 Phage Display of Proteases and Macromolecular Inhibitors
                                        by CHENG-I WANG et al.

4. Affinity Maturation of Proteins Displayed on Surface of M13 Bacteriophage as
Major Coat Protein Fusions
                                        by B.L. ROBERTS et al.

5. Screening of Phage Antibody Libraries
                                        by J.L. HARRISON et al.

6. Immunization with Phage-Displayed Mimotopes
                                        by G. GALFRE' et al.

7. Phage-Displayed Peptides as Tools for Characterization of Human Sera
                                        by F. FELICI et al.

8. Phage Display Methods for selecting Zinc Finger Proteins with DNA-Binding
Specificities
                                        by E.J. REBAR et al.

9. In Vitro Genetic Analysis of RNA-Binding Proteins Using Phage Display
Libraries
                                        by I.A. LAIRD-OFFRINGA and J.G. BELASCO



        Section II. lac Repressor Fusion Proteins

10. Screening of Peptide Libraries Linked to lac Repressor
                                        by P.J. SCHATZ et al.



          Section III. Libraries on Polysomes

11. Cell-Free Synthesis of Peptide Libraries Displayed on Polysomes
                                        by L.C. MATTHEAKIS et al.



          Section IV. Peptide Libraries

12. One Bead-One Compound Combinatorial Peptide Library: Different Types of
Screening
                                        by C.L. CHEN et al.

13. Generation and Use of Nonsupport-Bound Peptide and Peptidomimetic
Combinatorial Libraries
                                        by J.M. OSTRESH et al.

14. Combinatorial Chemistry: A Liquid-Phase Approach
                                        by K.D. JANDA and H. HAN

15. Preparation of Equimolar Mixtures of Peptides by Adjustment of Activated
Amino Acid Concentrations
                                        by K.M. IVANETICH and D.V. SANTI

16. Encoded Combinatorial Chemistry: Binary Coding Using Chemically Robust
Secondary Amine Tags 
                                        by ZHI-JIE NI et al.



          Section V. Nucleic Acid Libraries

17. A SELEX Primer
                                        by T. FITZWATER and B. POLISKY

18. Identifying Consensus Patterns and Secondary Structure in SELEX Sequence
Sets
                                        by J.P. DAVIS et al.

19. Affinity Selection-Amplification from Randomized Ribooligonucleotide Pools
                                        by J. CIESIOLKA et al.

20. In Vitro Selection of Nucleic Acid Aptamers That Bind Proteins
                                        by R.C. CONRAD et al.

21. Randomization and Selection of RNA to Identify Targets for RRM RNA-Binding
Proteins and Antibodies
                                        by J.D. KEENE

22. Selection of Aminoacylated tRNAs from RNA Libraries Having Randomized
Acceptor Stem Sequences: Using Old Dogs to Perform New Tricks
                                        by J.R. SAMPSON and M.E. SARKS

23. In Vitro Evolution of Randomized Ribozymes
                                        by J. TSANG and G.F. JOYCE

24. Peptide Nucleic Acids: A New Dimension to Peptide Libraries and Aptamers
                                        by P.E. NIELSEN



      Section VI. Other Small Molecule Libraries

25. Synthesis of N-Substituted Glycine Peptoid Libraries
                                        by G.M. FIGLIOZZI et al.

26. Synthesis and Evaluation of 1,4-Benzodiazepine Libraries
                                        by B.A. BUNIN et al.

From owner-repertoires@net.bio.net Wed Jun 19 23:00:00 1996
Path: biosci!daresbury!not-for-mail
From: Andrew Wallace <A.Wallace@Queens-Belfast.AC.UK>
Newsgroups: bionet.molecules.repertoires
Subject: Mirror Image Phage
Date: 20 Jun 1996 18:48:50 +0100
Lines: 30
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Distribution: bionet
Message-ID: <4qc2u2$an1@mserv1.dl.ac.uk>
Original-To: molreps@dl.ac.uk

      What do you think of the recent paper in Science where they
      used L-amino acid-bearing phage against a synthetic D-aa
      protein ligand, took the binding sequence, synthesised a
      retro peptide sequence of D-aas and found that it bound to
      the corresponding L-aa protein?

      Sounds confusing, doesn't it.

      They seem to be saying that the ligand

      ACDEFGH

      binding to a site on a D-aa receptor will be the mirror image
      situation to peptide 

      hgfedca 

      (using lower case for D-aas) binding to the corresponding
      site on an L-aa receptor.

      Does this make sense? What does this imply for the peptides,
      would it be true that ACDEFGH and hgfedca would adopt the
      same 3D structure but bind in opposite orientations, perhaps?

      Andrew


 ==================================================================
 Andrew Wallace, Ph.D., Queen's University Belfast, N. Ireland (UK)
 a.wallace@qub.ac.uk      http://www.qub.ac.uk/b&bchem/rbiochem.htm

From owner-repertoires@net.bio.net Wed Jun 19 23:00:00 1996
Path: biosci!daresbury!not-for-mail
From: Andrew Wallace <A.Wallace@Queens-Belfast.AC.UK>
Newsgroups: bionet.molecules.repertoires
Subject: Re: Methods in Enzymology - Volume 267
Date: 20 Jun 1996 18:19:00 +0100
Lines: 27
Sender: lpddist@mserv1.dl.ac.uk
Distribution: bionet
Message-ID: <4qc164$8f3@mserv1.dl.ac.uk>
Original-To: molreps@dl.ac.uk

>-----------------------------------------------------------
>
>Methods in Enzymology
>
>Volume 267
>
>Combinatorial Chemistry
>
>EDITED BY
>John N. Abelson
>
>ACADEMIC PRESS, 1996
>San Diego New York Boston London Sydney Tokyo Toronto
>

      Looks good, does anyone know if it is possible to order
      individual titles from the Methods in Enzymology series?
      I would have thought it is but the library/bookshop here at
      QUB told me that Academic Press wouldn't allow it! (seems odd
      to me).

      Andrew


 ==================================================================
 Andrew Wallace, Ph.D., Queen's University Belfast, N. Ireland (UK)
 a.wallace@qub.ac.uk      http://www.qub.ac.uk/b&bchem/rbiochem.htm

From owner-repertoires@net.bio.net Thu Jun 20 23:00:00 1996
Path: biosci!rutgers!sgigate.sgi.com!esiee.fr!jussieu.fr!news.sri.ucl.ac.be!news.belnet.be!swsbe6.switch.ch!scsing.switch.ch!rzunews.unizh.ch!newsadm
From: simone@erdw.ethz.ch
Newsgroups: bionet.molecules.repertoires
Subject: Re: Methods in Enzymology - Volume 267
Date: Fri, 21 Jun 1996 10:52:10 +0200
Organization: University of Zurich, Switzerland
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Does anybody know when volume 267 is going to be out?
(Our library has only got up to volume 264)

From owner-repertoires@net.bio.net Thu Jun 20 23:00:00 1996
Path: biosci!daresbury!not-for-mail
From: Franco Felici <FELICI@irbm.it>
Newsgroups: bionet.molecules.repertoires
Subject: Re: Methods in Enzymology - Volume 267
Date: 21 Jun 1996 10:46:18 +0100
Lines: 17
Sender: lpddist@mserv1.dl.ac.uk
Distribution: bionet
Message-ID: <4qdr1a$efv@mserv1.dl.ac.uk>
Original-To: molreps@dl.ac.uk

Well, I have a copy of the above Volume in my hands... We have received
few days ago a complimentary copy from the publisher. I guess that it
should be very soon available (if not already).

You could ask directly:

Academic Press, Inc. 6277 Sea Harbor Drive, Orlando, FL 32887 USA
Tel. 407-345-2000   Fax: 407-345-4058
or 
Academic Press, Inc. 525 B Street, Suite 1900, San Diego CA 92101-4495 USA
or 
Academic Press Limited, 24-28 Oval Road, London NW1 7DX England


Best wishes,

Franco Felici

From owner-repertoires@net.bio.net Sun Jun 23 23:00:00 1996
Path: biosci!daresbury!not-for-mail
From: Andrew Wallace <A.Wallace@Queens-Belfast.AC.UK>
Newsgroups: bionet.molecules.repertoires
Subject: RE: Mirror Image Phage
Date: 24 Jun 1996 17:05:02 +0100
Lines: 29
Sender: lpddist@mserv1.dl.ac.uk
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Message-ID: <4qmebe$q25@mserv1.dl.ac.uk>
Original-To: molreps@dl.ac.uk

      Hmmm....Yes, I think AndrewB is right, the authors of the
      Science paper said that 

      ACDEF bound to D-aa receptor

      so

      acdef will bind to L-aa receptor, not fedca as I said.

      This makes sense, as ACDEF and acdef will be mirror images of
      each other. I think I was getting mixed up with a paper in
      Nature Structural Biology on IgE receptor antagonists, where
      they seemed to be saying that

      cyclo-(ACEDF)

      has the same structure as

      cyclo-(fedca)

      which looks reasonable to me, but this is another story...

      Sorry about the confusion caused.

      Andrew

 ==================================================================
 Andrew Wallace, Ph.D., Queen's University Belfast, N. Ireland (UK)
 a.wallace@qub.ac.uk      http://www.qub.ac.uk/b&bchem/rbiochem.htm

From owner-repertoires@net.bio.net Tue Jun 25 23:00:00 1996
Path: biosci!daresbury!yama.mcc.ac.uk!zippy.dct.ac.uk!str-ccsun!strath-cs!queens-belfast.ac.uk!queens-belfast.ac.uk!nntp
Newsgroups: bionet.molecules.repertoires
Subject: Re: Methods in Enzymology - Volume 267
Message-ID: <1996Jun25.123115.6719@queens-belfast.ac.uk>
From: Andrew Wallace <a.wallace@queens-belfast.ac.uk>
Date: 25 Jun 96 12:31:14 GMT
References: <4qdr1a$efv@mserv1.dl.ac.uk>
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For those in the UK, you can contact Academic Press at Harcourt, Brace 
and Jovanovich, the publishers on 0171-267-4466

The ISBN for Methods in Enzymology - Volume 267 is

0121-821-684

|======================================================================|
| Andrew Wallace,Ph.D., Queen's University Belfast,  N. Ireland (UK)   |
| a.wallace@qub.ac.uk      http://www.qub.ac.uk/b&bchem/rbiochem.htm   |
|======================================================================|



From owner-repertoires@net.bio.net Thu Jun 27 23:00:00 1996
Path: biosci!daresbury!not-for-mail
From: Andrew Wallace <a.wallace@qub.ac.uk>
Newsgroups: bionet.molecules.repertoires
Subject: Molreps FAQ for July 1996
Date: 28 Jun 1996 19:00:21 +0100
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Original-To: molreps@dl.ac.uk


      M O L R E P S   F R E Q U E N T L Y   A S K E D   Q U E S T I O N S
      *************   *******************   *********   *****************


      **1 Where can I obtain libraries?**

      1.1 _Phage Libraries_
       	   You can try approaching the following people and
           organisations:

      1.1.1 pIII/6-mer, pIII/15-mer, pVIII-4/15-mer libraries:
            George Smith, University of Missouri, FAX +1-573-882-0123

      1.1.2 pVIII/9-mer, pVIII/9-merCys and pVIII/zinc-finger
            phagemid libraries:
            Alessandra Luzzago, IRBM P. Angeletti, luzzago@irbm.it
            Franco Felici, IRBM P. Angeletti, felici@irbm.it
            (NON-COMMERCIAL USERS ONLY)

      1.1.3 Antibody scFvs with synthetic CDRs:
            Greg Winter, MRC-LMB Cambridge, gw@mrc-lmb.cam.ac.uk
            (NON-COMMERCIAL USERS ONLY)

      1.1.4 Commercial Sources:
            Stratagene (Fab fragments in phage lambda)
            Affymax
            Pharmacia
            Cambridge Antibody Technology
            New England Biolabs (pIII/7-mer). (NEB catalog, p.166).
             see also this URL -> http://vent.neb.com/neb/phd/phd.html




      1.2 _Synthetic Peptide Libraries_

      1.2.1 Commercial Sources:
            Affymax
            Selectide
            Chiron Corporation

            Most of the major peptide companies will custom-synthesise a
            library to your requirements.



      1.3 _Nucleic Acid Libraries_ (Aptamers)

      1.3.1 Jack Szostak at Harvard medical school?
      1.3.2 NEXUS corporation (Larry Gold)?




      1.4 _Organic Chemical Libraries_

      1.4.1 Affymax?
      1.4.2 Parke-Davis (DIVERSOMERS)?







      **2) Where can I get anti-phage antibodies?**

      2.1 anti-pIII MAb from Michael Tesar
          mte@venus.gbf-braunschweig.d400.de

      2.2 anti-pIII polyclonals from GATC, a German company,
          FAX +49-7531-57313   TEL +49-7531-57204

      2.3 rabbit anti-M13 from Stratagene.






      **3) How can I make my own libraries?**


      3.1 _Phage Libraries_
           You can obtain suitable vectors and strains from most of 
           the sources in 1).

           For phagemid work you can get XL-1 Blue cells from
           Stratagene and M13K07 helper phage from Pharmacia.



      3.2 _Synthetic Peptide Libraries_


      3.2.1 Manual synthesis

            Houghten's "Tea Bag" method
            Geysen's "Pin" method

            Both of these can be adapted to produce either
            support-bound or soluble libraries.



      3.2.2 Automated synthesis

            Chiron Corporation (Zuckermann)
            Advanced Chemtech (Commercial robot for 75K sterling)




      3.3 _Nucleic Acid Libraries_

      3.3.1 PCR methods





      3.4 _Organic Chemical Libraries_

      3.4.1 Manual synthesis

      3.4.2 Automated synthesis (Advanced Chemtech)







      **4) How can I analyse the results of my selection?**



      4.1 Insert sequencing (phage libraries)

      4.2 Micropanning 
                (Smith and Scott, Methods Enzymol. (1993) 217:228-257)

      4.3 Dot-blotting
                (Felici et al., J. Mol. Biol. (1991) 222:301-310)

      4.4 ELISA 
                (Smith and Scott, Methods Enzymol. (1993) 217:228-257)
                (Dente et al. Gene (1994) 148:7-13)

      4.5 Colony immunoscreening 
                (Christian et al. J. Mol. Biol. (1992) 227, 711-718)
                (Felici et al. Gene (1993) 128, 21-27)

      4.5 Plaque immunoscreening
                (Luzzago et al., Gene (1993) 128:51-57)
                (Felici et al., Methods Enzymol. (1996) 267:116-129)







      **5) Are there any World Wide Web (WWW) sites about molreps?



      5.1  http://www.bio.net/
		- The BIOSCI web site itself (MOLREPS message archive)

	
      5.2  http://bionmr1.rug.ac.be/chemistry/overview.html
		- A useful chemistry site


      5.3  http://vesta.pd.com/
		- Site for the journal MOLECULAR DIVERSITY

 
      5.4  http://www.mrc-cpe.cam.ac.uk/imt-doc/vbase-home-page.html
          	- Immunoglobulin v-gene database


      5.5  http://molbio.info.nih.gov/molbio/desk.html
		- Molecular biologists desk reference


      5.6  http://www.Kairos-scientific.com/
		- Kairos scientific home page


      5.7  http://www-lmmb.ncifcrf.gov/~toms/
		- Tom Schneider's Theory of Molecular Machines


      5.8  http://www.ebi.ac.uk/
                    - The European Bioinformatics Institute (EBI)

 
      5.9  http://www.ebi.ac.uk/primers_home.html
                    - PCR primers database at EBI


      5.10 http://aminoacid.bri.nrc.ca:1125/
                    - Database of building blocks for library
                      synthesis


      5.11 http://vent.neb.com/neb/phd/phd.html
                    - PHD commercial phage library at 
                      New England Biolabs


      5.12 ftp://ftp.netcom.com/pub/qu/quincicc/maxim.html
                    - Another commercial library source



------------------------------------------------------------------
Andrew Wallace, Ph.D,  Queen's University Belfast, N. Ireland (UK)
a.wallace@qub.ac.uk      http://www.qub.ac.uk/b&bchem/rbiochem.htm



From owner-repertoires@net.bio.net Thu Jun 27 23:00:00 1996
Path: biosci!internet!biosci!not-for-mail
From: biohelp (BIOSCI Administrator)
Newsgroups: bionet.molecules.repertoires
Subject: IMPORTANT - BIOSCI Fundraising Update!
Date: 28 Jun 1996 02:01:02 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 154
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <199606280900.CAA21861@net.bio.net>
NNTP-Posting-Host: net.bio.net

	    BIOSCI is about halfway to its funding goal!!

I'm interrupting the usual monthly posting of the BIOSCI miniFAQ to
bring you up to date on BIOSCI fundraising progress, a topic of
concern to your future use of this resource.  Thank you in advance for
taking the time to read this message carefully.

Last year we announced that BIOSCI was going to adopt the U.S. Public
Broadcasting System model to fund its operations after our DOE/NSF
grant runs out later this year.  Unlike PBS, we are not soliciting
contributions from users; we are only selling ads on our Web pages
solely to cover our operating costs.  Our goal is to seek sponsorships
until we build up an operating reserve of about $100,000 and then
cease further promotions until we need to build the reserve back up.
(The accountants among our readership will be familiar with the
problem of deferred revenue which we can not safely utilize until ads
have been displayed for a period of time.)  We are only about halfway
to our funding goal and need to raise further funds to avoid having to
curtail services at net.bio.net.  Fundraising is time-consuming,
however, and we need your help as explained further below.

Our operating costs consist of our network connection, phone lines,
hardware maintenance (we will be getting newer and faster hardware
soon!), plus 0.7 FTE of salaries covering UNIX systems admin,
technical support, quality assurance, i.e., testing, of our system,
and administrative costs (such as the time it takes to actually
find/write/call potential sponsors and raise money!).  Although the
BIOSCI staff does get compensated for a portion of the work that they
do, this project has always received a lot of free after-hours and
"vacation" time labor, so we hope that no one will begrudge the time
that we do charge to the project to serve you.  All of the three
part-time staff members, Dave Mack, Julie Lawrence, and myself, have
full time day jobs and families in addition to working hard to keep
this service running for all of you.  Julie and Dave Mack are
subcontractors for BIOSCI; my time that is charged to the project
defrays a portion of my regular salary instead of adding to my income.

Besides having to relocate the project, we were very busy this last
year building new infrastructure such as our WWW hypermail interface
to the system.  This was released last December along with scores of
WAIS indices for the newsgroups.  Virtually everything is complete,
although we do continue to find and fix bugs (many through your
helpful feedback!).  We are still having some problems with our WAIS
indexing.  The archives continue to grow rapidly.  We are running over
100 indexes now versus three previously and any systems crashes cause
greater havoc with the indexing than before!  We are still working to
fix this as fast as our resources permit and appreciate your patience,
but we have been able to automate a lot of the infrastructure to
reduce labor as compared to past requirements.

We have also implemented new software to make moderation of
BIOSCI/bionet newsgroups much easier and combat the growing problem of
Internet junk mail and USENET "spamming."  About 20% of our groups are
now moderated, many of them by the BIOSCI staff!  This, for example,
made a major difference last year in the quality of content in our
EMPLOYMENT/bionet.jobs.offered newsgroup which many commercial
concerns and recruiting firms are using **without charge** to recruit
candidates for positions in the biological sciences.

We are also now in a position to have sponsors for individual
newsgroups as you will have noticed if you have visited
http://www.bio.net/ and clicked on "Access the BIOSCI/bionet
newsgroups" recently.

So, how can you help??
----------------------

As noted above it can take a lot of time to contact potential sponsors
if I have to do it all myself.  Our request is quite simple.  You can
do two important things which will take very little time for you
individually.  

First, please use our WWW system at http://www.bio.net/ to access the
archives.  You can now post or reply to messages via your Web browser.
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.

Our hope is to quickly raise several large corporate/institutional
sponsors on our heavily-used WWW locations (some stats appended
below), and then end this sponsorship campaign so that our resources
can continue to be used for service provision, not fundraising.  Many
of our specialty newsgroup WWW archives are still used by small
communities of scientists (and they haven't been heavily promoted
yet).  While these may be valuable niche markets to some advertisers,
it will generate more labor and overhead having to find these
sponsors, fairly price the locations, and deal with lots of smaller
sponsorships than fewer mid-to large sponsors.  We are striving to
keep our operation as lean and efficient as possible since we are not
trying to make careers out of running BIOSCI.  We are trying if at all
possible to avoid the administrative overhead entailed with processing
lots of small payments to reach our fundraising goals.

I'd like to thank all of you for your help in advance. In helping us,
you are also helping yourselves, not only in keeping this resource
available for all of the both large and small research communities
that we serve, but also by alleviating the need for us to go back and
compete with researchers for tight grant dollars!  We promised NSF
when we were awarded the BIOSCI grant that we would carry out this
mission to make the service self-supporting.  With your help, we will
succeed in continuing BIOSCI's work into its second decade.  Thank you
very much!

				Sincerely,

				Dave Kristofferson
				BIOSCI/bionet Manager

				biosci-help@net.bio.net


A list of our prime WWW sponsorship locations follow.  Please contact
us for further details.
----------------------------------------------------------------------

The overall BIOSCI WWW pages are currently visited by users from close
to 5500 unique computer hosts per week.  Web servers only log the
Internet computer/host name and frequently more than one individual
can connect to us from a particular host.

Main home page, http://www.bio.net, visited recently by about 2100
unique hosts per week

Main Newsgroups archives page, http://www.bio.net/archives.html,
visited recently by about 1200 Unique hosts per week

BIO-JOURNALS archive page, http://www.bio.net/BIO-JOURNALS.html,
visited recently by about 1000 unique hosts per week.

EMPLOYMENT archive pages: http://www.bio.net:80/hypermail/EMPLOYMENT/ 
and monthly header pages, visited recently by about 800 unique hosts
per week.

Address database search page, http://www.bio.net/addrsearch.html,
visited recently by about 450 unique hosts per week.

Methods newsgroup archive pages, http://www.bio.net:80/hypermail/METHDS-
REAGNTS/ and monthly header pages, visited recently by about 350
unique hosts per week.

Ads can also be displayed on various combinations of other
BIOSCI/bionet newsgroups.  Please contact us at
biosci-help@net.bio.net for details.
----------------------------------------------------------------------

From owner-repertoires@net.bio.net Sun Jun 30 23:00:00 1996
Path: biosci!daresbury!not-for-mail
From: Andrew Wallace <a.wallace@qub.ac.uk>
Newsgroups: bionet.molecules.repertoires
Subject: Molreps FAQ for July 1996
Date: 1 Jul 1996 11:04:50 +0100
Lines: 229
Sender: lpddist@mserv1.dl.ac.uk
Distribution: bionet
Message-ID: <4r87s2$7lo@mserv1.dl.ac.uk>
MIME-Version: 1.0
X-Authentication: none
Original-To: molreps@dl.ac.uk

      M O L R E P S   F R E Q U E N T L Y   A S K E D   Q U E S T I O N S
      *************   *******************   *********   *****************


      **1 Where can I obtain libraries?**

      1.1 _Phage Libraries_
       	   You can try approaching the following people and
           organisations:


      1.1.1 pIII/6-mer, pIII/15-mer, pVIII-4/15-mer libraries:
            George Smith, University of Missouri, FAX +1-573-882-0123


      1.1.2 pVIII/9-mer, pVIII/9-merCys and pVIII/zinc-finger
            phagemid libraries:
            Alessandra Luzzago, IRBM P. Angeletti, luzzago@irbm.it
            Franco Felici, IRBM P. Angeletti, felici@irbm.it
            (NON-COMMERCIAL USERS ONLY)


      1.1.3 Antibody scFvs with synthetic CDRs:
            Greg Winter, MRC-LMB Cambridge, gw@mrc-lmb.cam.ac.uk
            (NON-COMMERCIAL USERS ONLY)


      1.1.4 Commercial Sources:
            Stratagene (Fab fragments in phage lambda)
            Affymax
            Pharmacia
            Cambridge Antibody Technology
            New England Biolabs (pIII/7-mer). (NEB catalog, p.166).
             see also this URL -> http://vent.neb.com/neb/phd/phd.html




      1.2 _Synthetic Peptide Libraries_

      1.2.1 Commercial Sources:
            Affymax
            Selectide
            Chiron Corporation

            Most of the major peptide companies will custom-synthesise a
            library to your requirements.



      1.3 _Nucleic Acid Libraries_ (Aptamers)

      1.3.1 Jack Szostak at Harvard medical school?
      1.3.2 NEXUS corporation (Larry Gold)?




      1.4 _Organic Chemical Libraries_

      1.4.1 Affymax?
      1.4.2 Parke-Davis (DIVERSOMERS)?







      **2) Where can I get anti-phage antibodies?**

      2.1 anti-pIII MAb from Michael Tesar
          mte@venus.gbf-braunschweig.d400.de

      2.2 anti-pIII polyclonals from GATC, a German company,
          FAX +49-7531-57313   TEL +49-7531-57204

      2.3 rabbit anti-M13 from Stratagene.






      **3) How can I make my own libraries?**


      3.1 _Phage Libraries_
           You can obtain suitable vectors and strains from most of 
           the sources in 1).

           For phagemid work you can get XL-1 Blue cells from
           Stratagene and M13K07 helper phage from Pharmacia.



      3.2 _Synthetic Peptide Libraries_


      3.2.1 Manual synthesis

            Houghten's "Tea Bag" method
            Geysen's "Pin" method

            Both of these can be adapted to produce either
            support-bound or soluble libraries.



      3.2.2 Automated synthesis

            Chiron Corporation (Zuckermann)
            Advanced Chemtech (Commercial robot for 75K sterling)




      3.3 _Nucleic Acid Libraries_

      3.3.1 PCR methods





      3.4 _Organic Chemical Libraries_

      3.4.1 Manual synthesis

      3.4.2 Automated synthesis (Advanced Chemtech)







      **4) How can I analyse the results of my selection?**



      4.1 Insert sequencing (phage libraries)

      4.2 Micropanning 
                (Smith and Scott, Methods Enzymol. (1993) 217:228-257)

      4.3 Dot-blotting
                (Felici et al., J. Mol. Biol. (1991) 222:301-310)

      4.4 ELISA 
                (Smith and Scott, Methods Enzymol. (1993) 217:228-257)
                (Dente et al. Gene (1994) 148:7-13)

      4.5 Colony immunoscreening 
                (Christian et al. J. Mol. Biol. (1992) 227, 711-718)
                (Felici et al. Gene (1993) 128, 21-27)

      4.5 Plaque immunoscreening
                (Luzzago et al., Gene (1993) 128:51-57)
                (Felici et al., Methods Enzymol. (1996) 267:116-129)







      **5) Are there any World Wide Web (WWW) sites about molreps?**



      5.1  http://www.bio.net/
		- The BIOSCI web site itself (MOLREPS message archive)

	
      5.2  http://bionmr1.rug.ac.be/chemistry/overview.html
		- A useful chemistry site


      5.3  http://vesta.pd.com/
		- Site for the journal MOLECULAR DIVERSITY

 
      5.4  http://www.mrc-cpe.cam.ac.uk/imt-doc/vbase-home-page.html
          	- Immunoglobulin v-gene database


      5.5  http://molbio.info.nih.gov/molbio/desk.html
		- Molecular biologists desk reference


      5.6  http://www.Kairos-scientific.com/
		- Kairos scientific home page


      5.7  http://www-lmmb.ncifcrf.gov/~toms/
		- Tom Schneider's Theory of Molecular Machines


      5.8  http://www.ebi.ac.uk/
                    - The European Bioinformatics Institute (EBI)

 
      5.9  http://www.ebi.ac.uk/primers_home.html
                    - PCR primers database at EBI


      5.10 http://aminoacid.bri.nrc.ca:1125/
                    - Database of building blocks for library
                      synthesis


      5.11 http://vent.neb.com/neb/phd/phd.html
                    - PHD commercial phage library at 
                      New England Biolabs


>      5.12 ftp://ftp.netcom.com/pub/qu/quincicc/maxim.html
>                    - Another commercial library source
>      This link seems to be broken.


As usual, all comments and suggestions or corrections are welcome.
Andrew
------------------------------------------------------------------
Andrew Wallace, Ph.D,  Queen's University Belfast, N. Ireland (UK)
a.wallace@qub.ac.uk      http://www.qub.ac.uk/b&bchem/rbiochem.htm



