From owner-7tms_r@net.bio.net Tue Apr 01 23:00:00 1997
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From: David_L._Guarraia_at_MU-HSC-PHARM-PO1@EXT.MISSOURI.EDU
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From owner-7tms_r@net.bio.net Tue Apr 01 23:00:00 1997
Path: biosci!VIOLET.INCM.U-NANCY.FR!poda
From: poda@VIOLET.INCM.U-NANCY.FR (Gennady PODA)
Newsgroups: bionet.molbio.proteins.7tms_r
Subject: 7tms_r: HIV and opiates
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Dear Netters,

It is known that morphine and other narcotics alter the function of human
T lymphocytes and monocytes and may lead to activation of HIV infection
(ex., Squinto SP, et al. AIDS Res Hum Retroviruses, 6(10):1163-1168,
1990). Moreover, potentiation of HIV growth by morphine was antagonized by
naloxone and beta-funaltrexamine (opioid antagonists) (Peterson PK, et al.
AIDS 4(9):869-873, 1990). This means that opiate systems involved somehow
in HIV pathogenesis. Did anyone investigate possible mechanisms?

One of the possibilities can be direct binding of opiates to chemokine
receptors (found to be cofactors for HIV and host cell membrane fusion).
So the question, has anyone seen (or measured) binding constants of opiate
ligands (antagonists or agonists) to the chemokine receptors such as
CXCR-4 and CCR-5, etc.? This binding may be rather non specific but even
so... 

Any hints or references would be greatly appreciated. I will summarize 
the answers.

Best wishes and many thanks for your participation,

Gennady




************************************************************
Dr. Gennady PODA

Laboratoire de Chimie theorique (UA 510 du C.N.R.S.)
Universite Henri Poincare, Nancy-I
Faculte des Sciences - Domaine scientifique Victor Grignard
B.P. 239 - 54500 Vandoeuvre-les-Nancy Cedex France

Fax : + 33 (0)3.83.91.25.30   E-mail : poda@incm.u-nancy.fr
************************************************************


From owner-7tms_r@net.bio.net Tue Apr 01 23:00:00 1997
Path: biosci!cochin.inserm.fr!petit
From: petit@cochin.inserm.fr (Laurence Petit)
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SUBSCRIBE 7TMS

____________________________________________________________________________
Jerome GROS
ICGM - UPR0415 CNRS     email : gros@cochin.inserm.fr    ***********
22, rue Mechain         Tel (33) 01 40 51 64 22/21       * BioDocs *

F-75014 PARIS           fax (33) 01 40 51 72 10          ***********

Serveur de BioDocs : http://157.136.20.60
____________________________________________________________________________



From owner-7tms_r@net.bio.net Tue Apr 01 23:00:00 1997
Path: biosci!agate!spool.mu.edu!uwm.edu!newsfeeds.sol.net!europa.clark.net!cpk-news-hub1.bbnplanet.com!news.bbnplanet.com!news-peer.gsl.net!news-paris.gsl.net!news.gsl.net!rain.fr!pressimage!news1.isdnet.net!usenet
From: "Christophe Guenin" <christophe.guenin@hol.fr>
Newsgroups: bionet.molbio.proteins.7tms_r
Subject: Antibody and G-Protein
Date: 2 Apr 1997 20:15:16 GMT
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I am looking for company which distribute antibody against the following
subunits : 
    G(alpha)q, 
    G(alpha)11, 
    G(alpha)14, 
    G(alpha)16,
    Gh

Reply on this news group or send a mail to christophe.guenin@hol.fr

Thanks
Sophie Lechevallier - SERVIER Labs.

From owner-7tms_r@net.bio.net Tue Apr 01 23:00:00 1997
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From owner-7tms_r@net.bio.net Tue Apr 01 23:00:00 1997
Path: biosci!BIOCSERVER.BIOC.CWRU.EDU!roth
From: roth@BIOCSERVER.BIOC.CWRU.EDU
Newsgroups: bionet.molbio.proteins.7tms_r
Subject: non-internalizing receptors
Date: 2 Apr 1997 08:50:02 -0800
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The following receptors were reported to *not* internalize following agonist 
exposure:

alpha2-adrenergic subtype (Kobilka lab)

somatostatin receptor subtype (J. Cell Biology 102: 878, 1986
JBC 261: 3571, 1986)

AT2 angiontensin II receptor

Someone mentioned that an antagonist causes internalization of the At1 
receptor and asked about other examples of antagonist-induced 
internalization.  We have demonstrated (Mol Pharmacol, 1996) that ketanserin 
(a 5-HT2A antagonist) causes modest internalization of the 5-HT2A receptor 
and have a manuscript in preparation demonstrating the same thing for 
clozapine (which also functions as an antagonist)








From owner-7tms_r@net.bio.net Tue Apr 01 23:00:00 1997
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From: watson_j@bms.com (John Watson)
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christophe.guenin@hol.fr (Christophe Guenin) wrote:

>I am looking for company which distribute antibody against the following
>subunits :
>    G(alpha)q,
>    G(alpha)11,
>    G(alpha)14,
>    G(alpha)16,
>    Gh

Let's see... Antisera against G(q) and G(11) you can get from Santa Cruz
Biotechnol (http://www.scbt.com/) or DuPont NEN
(http://www.nenlifesci.com/).  I haven't seen or heard of anyone selling
G(14) or G(h) antisera.  Commercial applications of G(16), including (as
far as I know) antisera,  has been licensed to Aurora Biosciences
(http://www.aurorabio.com/). For noncommercial use of G(16), you might try
Mel Simon's lab at Caltech (http://www.caltech.edu/).

Cheers,

AJW



From owner-7tms_r@net.bio.net Tue Apr 01 23:00:00 1997
Path: biosci!UMDNJ.EDU!pikielcl
From: pikielcl@UMDNJ.EDU ("Claudio Pikielny")
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Subject: post-doc
Date: 2 Apr 1997 13:28:38 -0800
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Post-doctoral position available.  We study Chemical Senses (olfaction,
taste and pheromone response) in Drosophila  at the genetic, biochemical,
cellular and behavioral levels.  Send CV and letters of recommendation to
Claudio Pikielny, Dept. of Neuroscience and Cell Biology, UMDNJ/Robert Wood
Johnson Medical School, 675 Hoes Lane, Piscataway NJ 08540.  e-mail:
pikielcl@umdnj.edu




From owner-7tms_r@net.bio.net Tue Apr 01 23:00:00 1997
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From: c680296@SHOWME.MISSOURI.EDU
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SUBSCRIBE

David M. Bourdon
Graduate Research Assistant
MU School of Medicine
Department of Pharmacology
tel:  573-882-1554
e-mail:  c680296@showme.missouri.edu
home page:  http://www.missouri.edu/~c680296/index.htm


From owner-7tms_r@net.bio.net Tue Apr 01 23:00:00 1997
Path: biosci!MED.UNR.EDU!buxton
From: buxton@MED.UNR.EDU ("Iain L. O. Buxton")
Newsgroups: bionet.molbio.proteins.7tms_r
Subject: Re: 7tms_r: HIV and opiates
Date: 2 Apr 1997 08:02:17 -0800
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Dear Dr. Poda:

I am intrigued with the question you pose.  Faced with a not so disimilar
issue with respect to muscarinic systems and NO synthase inhibitors, we
show that a not-so-high-affinity interaction can be an issue (Buxton, 
I.L.O., Cheek, D.J., Eckman, D.M., Westfall, D.P. Sanders, K.M. and  Keef,
K.D. (1993) NG-nitro-L-arginine methylester (L-NAME) and other alkyl
esters of arginine are muscarinic receptor antagonists. Circ. Res. 72:
387-395.)

We could look at this with you if you are interested?

Iain L. O. Buxton
Professor of Pharmacology/318
Associate Dean for Research
University of Nevada School of Medicine
Howard Medical Sciences Building Rm:216
Reno, NV 89557
Phone:  (702)784-1566
FAX:    (702)784-1620
buxton@med.unr.edu


On 2 Apr 1997, Gennady PODA wrote:

> Dear Netters,
> 
> It is known that morphine and other narcotics alter the function of human
> T lymphocytes and monocytes and may lead to activation of HIV infection
> (ex., Squinto SP, et al. AIDS Res Hum Retroviruses, 6(10):1163-1168,
> 1990). Moreover, potentiation of HIV growth by morphine was antagonized by
> naloxone and beta-funaltrexamine (opioid antagonists) (Peterson PK, et al.
> AIDS 4(9):869-873, 1990). This means that opiate systems involved somehow
> in HIV pathogenesis. Did anyone investigate possible mechanisms?
> 
> One of the possibilities can be direct binding of opiates to chemokine
> receptors (found to be cofactors for HIV and host cell membrane fusion).
> So the question, has anyone seen (or measured) binding constants of opiate
> ligands (antagonists or agonists) to the chemokine receptors such as
> CXCR-4 and CCR-5, etc.? This binding may be rather non specific but even
> so... 
> 
> Any hints or references would be greatly appreciated. I will summarize 
> the answers.
> 
> Best wishes and many thanks for your participation,
> 
> Gennady
> 
> 
> 
> 
> ************************************************************
> Dr. Gennady PODA
> 
> Laboratoire de Chimie theorique (UA 510 du C.N.R.S.)
> Universite Henri Poincare, Nancy-I
> Faculte des Sciences - Domaine scientifique Victor Grignard
> B.P. 239 - 54500 Vandoeuvre-les-Nancy Cedex France
> 
> Fax : + 33 (0)3.83.91.25.30   E-mail : poda@incm.u-nancy.fr
> ************************************************************
> 
> 


From owner-7tms_r@net.bio.net Wed Apr 02 23:00:00 1997
Path: biosci!rutgers.rutgers.edu!gatech!csulb.edu!hammer.uoregon.edu!news-xfer.netaxs.com!cpk-news-hub1.bbnplanet.com!news.bbnplanet.com!news-peer.gsl.net!news-paris.gsl.net!news.gsl.net!rain.fr!pressimage!news1.isdnet.net!usenet
From: "Christophe Guenin" <christophe.guenin@hol.fr>
Newsgroups: bionet.molbio.proteins.7tms_r
Subject: Receptors and G_Protein
Date: 3 Apr 1997 19:19:40 GMT
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Dear netters

I am looking for structures of the genes of the receptors coupled to G
Proteins


You can answer in this news group ou send a mail to
christophe.guenin@hol.fr
Best wishes and many thanks for your participation

Sophie-Penelope Lechevallier - SERVIER Labs

From owner-7tms_r@net.bio.net Wed Apr 02 23:00:00 1997
Path: biosci!cochin.inserm.fr!laurence.petit
From: laurence.petit@cochin.inserm.fr (Laurence Petit)
Newsgroups: bionet.molbio.proteins.7tms_r
Subject: subscribe 7tms_r
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subscribe 7tms_r

Laurence Petit
UPR 415
Institut Cochin de genetique Moleculaire
22 rue Mechain
75014 Paris

Phone : (33-1) 40-51-64-39
Fax     : (33-1) 40-51-72-10
e mail : laurence.petit@cochin.inserm.fr



From owner-7tms_r@net.bio.net Wed Apr 02 23:00:00 1997
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From: Keith_Hutchison@discovery.umeres.maine.edu (Keith Hutchison)
Newsgroups: bionet.molbio.proteins.7tms_r
Subject: Faculty Position - Protein Biochemist
Date: Thu, 3 Apr 1997 08:58:23 -0500
Organization: University of Maine
Lines: 18
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X-Gateway: NASTA Gate 1.18 for FirstClass(R)

PROTEIN BIOCHEMIST:  The Department of Biochemistry, Microbiology and
Molecular Biology at the University of Maine seeks  a biochemist with
research interests in protein-protein or protein-nucleic acid
interactions to fill a tenure track position at either the Assistant or
Associate Professor level, available September 1, 1997.  Additional
research experience in the molecular genetics or developmental biology
of aquatic organisms is desirable.  A Ph.D. and postdoctoral experience
are required.  The successful candidate will be expected to maintain a
vigorous, extramurally funded research program and contribute to
teaching of the undergraduate and graduate curricula in Biochemistry. 
Minimum salary is $40,000 per academic year. Send a cover letter, 
description of research interests, curriculum vitae and three letters
of recommendation to: Dr. Michael E. Vayda, Chair, Biochemistry Search
Committee,  5735 Hitchner-BMMB, University of Maine, Orono, ME 
04469-5735.  Review of applications will commence June 1, 1997 and
applications will be considered until a suitable candidate is located. 
Women and minorities are encouraged to apply.  The University of Maine
is an Affirmative Action/Equal Employment Opportunity Employer.

From owner-7tms_r@net.bio.net Wed Apr 02 23:00:00 1997
Path: biosci!agate!howland.erols.net!netnews.com!mr.net!newshub.tc.umn.edu!mayonews.mayo.edu!not-for-mail
From: Ram <Rao@mayo.edu>
Newsgroups: bionet.molbio.proteins.7tms_r
Subject: Re: non-internalizing receptors
Date: Thu, 03 Apr 1997 17:39:18 -0600
Organization: Mayo Foundation
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To: roth@BIOCSERVER.BIOC.CWRU.EDU

We have recently reported internalization of CCK receptor by an 
antagonist. The paper entitled" Antagonist stimulated internalization 
of the G protein coupled CCK receptor appears as a Accelerated 
Communication in the March issue of Molecular Pharmacology
Vol:51 Pg 357-362

From owner-7tms_r@net.bio.net Wed Apr 02 23:00:00 1997
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From: Ram <Rao@mayo.edu>
Newsgroups: bionet.molbio.proteins.7tms_r
Subject: Re: non-internalizing receptors
Date: Thu, 03 Apr 1997 17:40:41 -0600
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To: roth@BIOCSERVER.BIOC.CWRU.EDU

We have recently reported internalization of CCK receptor by an 
antagonist. The paper entitled" Antagonist stimulated internalization 
of the G protein coupled CCK receptor appears as a Accelerated 
Communication in the March issue of Molecular Pharmacology
Vol:51 Pg 357-362

From owner-7tms_r@net.bio.net Wed Apr 02 23:00:00 1997
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From: Ram <Rao@mayo.edu>
Newsgroups: bionet.molbio.proteins.7tms_r
Subject: Re: non-internalizing receptors
Date: Thu, 03 Apr 1997 17:40:12 -0600
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We have recently reported internalization of CCK receptor by an 
antagonist. The paper entitled" Antagonist stimulated internalization 
of the G protein coupled CCK receptor appears as a Accelerated 
Communication in the March issue of Molecular Pharmacology
Vol:51 Pg 357-362

From owner-7tms_r@net.bio.net Wed Apr 02 23:00:00 1997
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From: Ram <Rao@mayo.edu>
Newsgroups: bionet.molbio.proteins.7tms_r
Subject: Re: non-internalizing receptors
Date: Thu, 03 Apr 1997 17:39:43 -0600
Organization: Mayo Foundation
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To: roth@BIOCSERVER.BIOC.CWRU.EDU

We have recently reported internalization of CCK receptor by an 
antagonist. The paper entitled" Antagonist stimulated internalization 
of the G protein coupled CCK receptor appears as a Accelerated 
Communication in the March issue of Molecular Pharmacology
Vol:51 Pg 357-362

From owner-7tms_r@net.bio.net Thu Apr 03 23:00:00 1997
Path: biosci!mayo.edu!Rao
From: Rao@mayo.edu
Newsgroups: bionet.molbio.proteins.7tms_r
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--Boundary (ID z1VhsuqGtjtR1QQcBHpeaA)
Content-type: TEXT/PLAIN


We have recently reported internalization of CCK receptor by an
antagonist. The paper entitled" Antagonist stimulated internalization
of the G protein coupled CCK receptor appears as a Accelerated
Communication in the March issue of Molecular Pharmacology
Vol:51 Pg 357-362


--Boundary (ID z1VhsuqGtjtR1QQcBHpeaA)
Content-type: TEXT/PLAIN


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Date: Thu, 03 Apr 1997 17:39:43 -0600
From: Ram <Rao@mayo.edu>
Subject: Re: non-internalizing receptors
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From owner-7tms_r@net.bio.net Thu Apr 03 23:00:00 1997
Path: biosci!UMDNJ.EDU!howells
From: howells@UMDNJ.EDU ("Richard D. Howells, Ph.D.")
Newsgroups: bionet.molbio.proteins.7tms_r
Subject: Postdoctoral fellowship
Date: 4 Apr 1997 11:02:33 -0800
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A postdoctoral fellowship will soon become available for molecular
analysis of opioid receptor structure and function. Site-directed
mutagenesis and receptor chimeras are being used to study receptor
selectivity, activation, signal transduction coupling, and turnover (cf.
Wang et al., PNAS 92: 12436-12440, 1995; Shahrestanifar et al., J. Biol.
Chem. 271: 5505-5512, 1996; Neurochem. Res. 21: 1295-1299, 1996). Please
send CVs to Dr. Richard D. Howells, Department of Biochemistry &
Molecular Biology, UMD-New Jersey Medical School, 185 South Orange
Avenue, Newark, NJ 07103.

Richard D. Howells, Ph.D.
Associate Professor

From owner-7tms_r@net.bio.net Thu Apr 03 23:00:00 1997
Path: biosci!mayo.edu!Rao
From: Rao@mayo.edu
Newsgroups: bionet.molbio.proteins.7tms_r
Subject: Re: non-internalizing receptors
Date: 4 Apr 1997 16:58:35 -0800
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We have recently reported internalization of CCK receptor by an
antagonist. The paper entitled" Antagonist stimulated internalization
of the G protein coupled CCK receptor appears as a Accelerated
Communication in the March issue of Molecular Pharmacology
Vol:51 Pg 357-362


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From owner-7tms_r@net.bio.net Thu Apr 03 23:00:00 1997
Path: biosci!daresbury!not-for-mail
From: jpwscyto@pavilion.co.uk (Jon Waterman-Smith)
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Subject: Forthcoming Microphysiometry Symposium in Paris
Date: 4 Apr 1997 17:06:09 +0100
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Please find enclosed details regarding this forthcoming meeting in Paris.
If you wish to receive further information on this event, please call Rana
=46riend at MDL [+44 (0)1293 619579], and we will send you full registration
information.

The 1997 International Symposium on Microphysiometry and Fluorescent Cell
Analysis. Paris, France - April 28-30, 1997.

Paris in spring time...

We hope this will be a suitable location for the first International
Symposium on Microphysiometry and FLIPR.

Venue: The Hyatt Regency Paris Hotel, Charles de Gaulle, Paris.

The Hyatt is a superior hotel on the outskirts of Paris, 5 minutes from
Charles de Gaulle airport, and only 20 minutes from the heart of Paris,
with direct rail links from Charles de Gaulle.

Dates: Monday 28th to Wednesday 30th April 1997.

Registration: 5:00 p.m. to 7:00 p.m. on Sunday 27th and 8:00 a.m. to 9:00
a.m. on Monday 28th of April.

Travel: Many airlines provide direct International links to Paris, Charles
de Gaulle. The Hyatt provides a courtesy bus to the hotel from the airport.

Accomodation and registration costs: We have made a block booking at the
hotel for the period of this conference. The price for the rooms and
registration have been fixed as follows. If you wish to book rooms for the
Saturday evening as well, accomodation will be available:

Sunday 27th April - 950FF ( =A3110 or $180 ) room only.
Monday 28th April - 950FF ( =A3110 or $180 ) room only.
Tuesday 29th April - 950FF ( =A3110 or $180 ) room only.

A one-off registration fee of 850FF ( =A3100 or $165 ). Molecular Devices is
directly funding the majority of the costs associated with this conference,
but we need to charge a small registration fee to assist in contributing to
the cost of this event. All meals will be provided on the Monday, including
a gala dinner. A presentation for the most original contribution to
research presented at this Symposium will be given. All meals (except
evening meals)  on the Tuesday and Wednesday are also covered in the
registration fee. A pre-registration form will be distributed to all
members of the email list in the coming weeks, and we would ask that you
return this as soon as possible if you wish to register, to ensure
accomodation is reserved, as we are limited to the number of guarenteed
rooms.

=46inal Program:

Intl Symposium on Microphysiometry & Fluorometric Cellular Screening

Monday Morning, April 28, 1997

Opening Remarks                                                 8:40-8:50
Chairperson, Dr. Simon Pitchford,
Applications Manager, Molecular Devices, USA

G Protein-Coupled Receptors

Martyn Coldwell                                                 8:50-9:30
Smith-Kline Beecham, UK
martyn_coldwell-1@sbphrd.com
Evolution of microphysiometer screening methods for increased throughput
functional studies on cloned dopaminergic receptors. M

Natalio Vita                                                    9:30-10:10
Sanofi, France
natalio.vita@tls1.elfsanofi.fr
Neurotensin receptor pharmacology. -M

BREAK                                                           10:10-10:30

Damien O'Connell                                                10:30-11:10
Cork University, Ireland
damian@ucc.ie
Dopaminergic receptor activity in human proximal tubular cells as assessed
by microphysiometry. -M

Will Lachnit                                                    11:10-11:50
Roche Biosciences, CA, USA
wilheim.lachnit@roche.com
=46LIPR: Quantitative pharmacological characterization of
heterologously-expressed G-protein coupled receptors. - F

LUNCH                                                           11:50-1:00

Opening Remarks                                                 1:00-1:10
Chairperson, Dr.Martyn Coldwell
Smith-Kline Beecham, UK

Signal Transduction

John Raymond                                                    1:10-1:50
Med. Univ. South Carolina, USA
raymondj@musc.edu
Use of the Cytosensor Microphysiometer System to map G-protein signalling
pathways.

Norbert Fraeyman                                                1:50-2:30
Heymans Institute, Belgium
norbert.fraeyman@rug.ac.be
Involvement of protein kinase C in the signal transduction related to
M3-cholinergic receptor stimulation.

Josh Rabinowitz                                                 2:30-3:10
Stanford University, CA, USA
rabino@leland.stanford.edu
The Redox Microphysiometer: Linking Signal Transduction to Cellular Redox
Metabolism - M

BREAK                                                           3:10-3:30

Novel Target Identification

Jan Seelig
3:30-4:10
Biozentrum, Switzerland
seelig1@ubaclu.unibas.ch
New Drugs for the Na+/H+ Exchanger.  Inhibition constants and detection of
side effects.-M

Mark Parmentier                                                 4:10-4:50
Libre University, Belgium
mparment@ulb.ac.be
The identification and characterization of the chemokine receptor, CCR5.M

Dr. Yasufuni Murakami                                           4:50-5:30
RIKEN Institute, JAPAN
yasufumi@rtcmain.rtc.riken.go.jp
Towards systemic analysis of gene functions of fully sequenced genome.M

Tuesday Morning, April 29, 1997

Opening remarks                                                 8:00-8:10
Chairperson, John Raymond, M.D.
Medical University of South Carolina, USA

Ion Channels

Mark Wolfe                                                      8:10-8:50
Pharmacia-Upjohn Co., MI, USA
mark.l.wolfe@am.pnu.com
Development of Cell Based High-volume Assays Using the FLIPR System. F

David Rock                                                      8:50-9:30
Parke-Davis Research, MI, USA
rockd@aa.wl.com
Monitoring voltage- and ligand-gated ion channels in cultured neurons using
=46LIPR. - F


Immunology

Darren Smart                                                    9:30-10:10
Parke-Davis, UK
smartd@camb.wl.com
IL-1 receptor characterization.-M

BREAK                                                           10:10-10:30

Dale Carey                                                      10:30-11:10
CRC-CGF - WEHI, Australia
carey@wehi.edu.au
Analysis of Signalling Capacity of Truncation Mutants of the GM-CSF
Receptor =DF-chain using the Cytosensor Microphysiometer - M

Subhashani Arimilli                                             11:10-11:50
Anergen, Inc., CA, USA
sarimilli@anergen.com
Measurement of extracellular acdification rates in Transformed human
T-cells to evaluate structure-function correlation of antigenic epitope by
silicon microphysiometry. - M

LUNCH                                                           11:50-1:00

Opening Remarks                                                 1:00-1:10
Chairperson, Dr. Simon Pitchford
Applications Manager, Molecular Devices Corp.

Tissues & Primary Cell Lines

David Bristow                                                   1:10-1:50
Manchester University, UK
david.bristow@man.ac.uk
Measurement of GABAA receptor function in cultured cerebellar granule cells
using microphysiometry: a study of the mechanisms underlying benzodiazepine
tolerance.-M

Anthony Ford                                                    1:50-2:30
Roche Biosciences, CA, USA
anthony.ford@roche.com
Pharmacological characterization of muscarinic cholinoceptors in rat
submaxillary gland using microphysiometry.-M

Richard Pittner                                                 2:30-3:10
Amylin Pharmaceuticals, CA, USA
rpittner@amylin.com
Measurement of Acidification Rates and Hormone Secretion in Freshly
Isolated Cells in Primary Culture.-M

BREAK                                                           3:10-3:30

Diagnostic Applications

Bernard Fung                                                    3:30-4:10
Jules Stein Eye Institute, UCLA, USA
bkkfung@ucla.edu
Real-time Monitoring of Reduced =DF-Adrenergic Responses in Fibroblasts from
Patients with Pseudohypoparathyroidism.-M

Julie Bennett-Desmelik                                          4:10-4:50
Emory University, GA, USA
jbennett@gmm.gen.emory.edu
Microphysiometric Analysis of Mitochondrial Function in Intact Lymphoblasts
from Leber's Hereditary Optic Neuropathy.-M

Wednesday Morning,  April 30, 1997                               9:00-12:30

Chairperson, Dr. Simon Pitchford
Applications Manager, Molecular Devices Corp.

Open discussion on any aspects of microphysiometry and fluorometric
cellular screening.  Topics for discussion to be submitted by audience.

Poster sessions will run throughout the 3 days.

We look forward to an exciting and stimulating conference in Paris, and
hope you will have the opportunity to attend and participate.




Jon Waterman-Smith
European Biosensor Business Manager

Molecular Devices Ltd
Unit 6 Raleigh Court
Rutherford Way
Crawley
W.Sussex
RH10 2PD
UK
Tel: +44 1293 619579
=46ax: +44 1293 619586
email: jpwscyto@pavilion.co.uk



From owner-7tms_r@net.bio.net Thu Apr 03 23:00:00 1997
Path: biosci!mayo.edu!Rao
From: Rao@mayo.edu
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Subject: Re: non-internalizing receptors
Date: 4 Apr 1997 16:42:44 -0800
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We have recently reported internalization of CCK receptor by an
antagonist. The paper entitled" Antagonist stimulated internalization
of the G protein coupled CCK receptor appears as a Accelerated
Communication in the March issue of Molecular Pharmacology
Vol:51 Pg 357-362


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Date: Thu, 03 Apr 1997 17:39:18 -0600
From: Ram <Rao@mayo.edu>
Subject: Re: non-internalizing receptors
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From owner-7tms_r@net.bio.net Thu Apr 03 23:00:00 1997
Path: biosci!mayo.edu!Rao
From: Rao@mayo.edu
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Subject: Re: non-internalizing receptors
Date: 4 Apr 1997 16:53:59 -0800
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We have recently reported internalization of CCK receptor by an
antagonist. The paper entitled" Antagonist stimulated internalization
of the G protein coupled CCK receptor appears as a Accelerated
Communication in the March issue of Molecular Pharmacology
Vol:51 Pg 357-362


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Subject: Re: non-internalizing receptors
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From owner-7tms_r@net.bio.net Fri Apr 04 23:00:00 1997
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Subject: Re: non-internalizing receptors
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We have recently reported internalization of CCK receptor by an
antagonist. The paper entitled" Antagonist stimulated internalization
of the G protein coupled CCK receptor appears as a Accelerated
Communication in the March issue of Molecular Pharmacology
Vol:51 Pg 357-362


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Date: Thu, 03 Apr 1997 17:39:18 -0600
From: Ram <Rao@mayo.edu>
Subject: Re: non-internalizing receptors
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From owner-7tms_r@net.bio.net Fri Apr 04 23:00:00 1997
Path: biosci!EMBL-HEIDELBERG.DE!Gert.Vriend
From: Gert.Vriend@EMBL-HEIDELBERG.DE
Newsgroups: bionet.molbio.proteins.7tms_r
Subject: GPCR database update
Date: 5 Apr 1997 03:01:14 -0800
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Dear GPCR friends,

Many of you have look already at the GPCRDB. Some of you are very
regular users. This database can be found at:
http://swift.embl-heidelberg.de/7tm/

Now that Florence Horn has joined us, we can really start working 
on the GPCRDB. Florence has several years of experience in database
design, and it seems likely that her contribution will lead to a
much better GPCRDB. Her first contribution is that the update frequency
will now be once per two months, aiming at one update per day, a goal
that we hope to reach within two years.

On April 2-4 1997 the GPCRDB was updated. Much of this update was
now done automatically, but as many of the programs used were used
for the first time, some errors seem likely. Please report any errors
that are not yet documented in the pages themselves.

- We have added several hundred models.
- We have added several thousands of ligand binding constants
  (a kind gift from Philip Seeman, thanks).
- we have added models for the Class B receptors
- We have added viseur based snake-like plots for all Class A
  receptors, and these plots are hyperlinked to the GRAP mutation
  database (thanks to Fabien Campagne and Oyvind Edvardson)
- We have made the navigation through sequences and alignments
  more uniform.

(We means Florence, her Email address is Horn@EMBL-Heidelberg.DE)

Gert Vriend

From owner-7tms_r@net.bio.net Fri Apr 04 23:00:00 1997
Path: biosci!mayo.edu!Rao
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We have recently reported internalization of CCK receptor by an
antagonist. The paper entitled" Antagonist stimulated internalization
of the G protein coupled CCK receptor appears as a Accelerated
Communication in the March issue of Molecular Pharmacology
Vol:51 Pg 357-362


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From owner-7tms_r@net.bio.net Fri Apr 04 23:00:00 1997
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We have recently reported internalization of CCK receptor by an
antagonist. The paper entitled" Antagonist stimulated internalization
of the G protein coupled CCK receptor appears as a Accelerated
Communication in the March issue of Molecular Pharmacology
Vol:51 Pg 357-362


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From: Ram <Rao@mayo.edu>
Subject: Re: non-internalizing receptors
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We have recently reported internalization of CCK receptor by an
antagonist. The paper entitled" Antagonist stimulated internalization
of the G protein coupled CCK receptor appears as a Accelerated
Communication in the March issue of Molecular Pharmacology
Vol:51 Pg 357-362


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From: Ram <Rao@mayo.edu>
Subject: Re: non-internalizing receptors
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From owner-7tms_r@net.bio.net Fri Apr 04 23:00:00 1997
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We have recently reported internalization of CCK receptor by an
antagonist. The paper entitled" Antagonist stimulated internalization
of the G protein coupled CCK receptor appears as a Accelerated
Communication in the March issue of Molecular Pharmacology
Vol:51 Pg 357-362


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From owner-7tms_r@net.bio.net Fri Apr 04 23:00:00 1997
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We have recently reported internalization of CCK receptor by an
antagonist. The paper entitled" Antagonist stimulated internalization
of the G protein coupled CCK receptor appears as a Accelerated
Communication in the March issue of Molecular Pharmacology
Vol:51 Pg 357-362


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From owner-7tms_r@net.bio.net Fri Apr 04 23:00:00 1997
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We have recently reported internalization of CCK receptor by an
antagonist. The paper entitled" Antagonist stimulated internalization
of the G protein coupled CCK receptor appears as a Accelerated
Communication in the March issue of Molecular Pharmacology
Vol:51 Pg 357-362


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From owner-7tms_r@net.bio.net Fri Apr 04 23:00:00 1997
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We have recently reported internalization of CCK receptor by an
antagonist. The paper entitled" Antagonist stimulated internalization
of the G protein coupled CCK receptor appears as a Accelerated
Communication in the March issue of Molecular Pharmacology
Vol:51 Pg 357-362


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From owner-7tms_r@net.bio.net Fri Apr 04 23:00:00 1997
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We have recently reported internalization of CCK receptor by an
antagonist. The paper entitled" Antagonist stimulated internalization
of the G protein coupled CCK receptor appears as a Accelerated
Communication in the March issue of Molecular Pharmacology
Vol:51 Pg 357-362


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From owner-7tms_r@net.bio.net Fri Apr 04 23:00:00 1997
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We have recently reported internalization of CCK receptor by an
antagonist. The paper entitled" Antagonist stimulated internalization
of the G protein coupled CCK receptor appears as a Accelerated
Communication in the March issue of Molecular Pharmacology
Vol:51 Pg 357-362


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From owner-7tms_r@net.bio.net Fri Apr 04 23:00:00 1997
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We have recently reported internalization of CCK receptor by an
antagonist. The paper entitled" Antagonist stimulated internalization
of the G protein coupled CCK receptor appears as a Accelerated
Communication in the March issue of Molecular Pharmacology
Vol:51 Pg 357-362


--Boundary (ID SzO0nY8sL/TmZuBxspWS/w)
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From owner-7tms_r@net.bio.net Fri Apr 04 23:00:00 1997
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We have recently reported internalization of CCK receptor by an
antagonist. The paper entitled" Antagonist stimulated internalization
of the G protein coupled CCK receptor appears as a Accelerated
Communication in the March issue of Molecular Pharmacology
Vol:51 Pg 357-362


--Boundary (ID VeowBp7xXIeKo0RK/Fz2Jg)
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From owner-7tms_r@net.bio.net Fri Apr 04 23:00:00 1997
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We have recently reported internalization of CCK receptor by an
antagonist. The paper entitled" Antagonist stimulated internalization
of the G protein coupled CCK receptor appears as a Accelerated
Communication in the March issue of Molecular Pharmacology
Vol:51 Pg 357-362


--Boundary (ID DADVjBRKjXa+wJPIaDSP+Q)
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From owner-7tms_r@net.bio.net Mon Apr 07 23:00:00 1997
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We have recently reported internalization of CCK receptor by an
antagonist. The paper entitled" Antagonist stimulated internalization
of the G protein coupled CCK receptor appears as a Accelerated
Communication in the March issue of Molecular Pharmacology
Vol:51 Pg 357-362


--Boundary (ID pdsZ+gVB93PcZiBN+/2Z3Q)
Content-type: TEXT/PLAIN


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From owner-7tms_r@net.bio.net Mon Apr 07 23:00:00 1997
Path: biosci!mayo.edu!Rao.Rammohan
From: Rao.Rammohan@mayo.edu (R Rao)
Newsgroups: bionet.molbio.proteins.7tms_r
Subject: Sincere apologies
Date: 8 Apr 1997 16:06:59 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 35
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NNTP-Posting-Host: net.bio.net


Dear 7tms_r netters/subscribers,

With a right and sincere scientific earnest, I posted a mail to the above=
=20
newsgroup regarding =D2Antagonist mediated internalization  of a G protein=
=20
coupled receptor=D3. Unfortunately the message has been repeating  itself=
=20
over and over, resulting  in a flurry of the same message and cluttering=20
the e-mail of all subscribers.=20

I realize it is annoying, receiving  similar messages over 20 times but=20
honestly, it is not a deliberate  attempt in glorifying our publication=20
or our work.=20

I notified our institution=D5s Computing facility and after a thorough=20
check, I was informed that the problem is not from our side. I am told=20
that somewhere down the line the network went haywire resulting in these=20
erroneous repeat messages.

I have informed repeatedly the 7tm newsgroup=D5s help desk and I hope they=
=20
are rectifying the problem. Until then, kindly tolerate this barrage of=20
recurrent  messages.=20

I also appeal to one and all to desist from sending me abusive letters.=20
It is unbecoming of Lecturers/Asst Professors/Professors, who write=20
disdainful letters that carry  crude and raw language.=20

Finally I hope that this message does not travel the same way as my last on=
e

Rao.


From owner-7tms_r@net.bio.net Mon Apr 07 23:00:00 1997
Path: biosci!mayo.edu!Rao
From: Rao@mayo.edu
Newsgroups: bionet.molbio.proteins.7tms_r
Subject: Re: non-internalizing receptors
Date: 8 Apr 1997 15:08:35 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 40
Sender: daemon@net.bio.net
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NNTP-Posting-Host: net.bio.net


--Boundary (ID nO9jnDjzMcyKY/+YHc2E5Q)
Content-type: TEXT/PLAIN


We have recently reported internalization of CCK receptor by an
antagonist. The paper entitled" Antagonist stimulated internalization
of the G protein coupled CCK receptor appears as a Accelerated
Communication in the March issue of Molecular Pharmacology
Vol:51 Pg 357-362


--Boundary (ID nO9jnDjzMcyKY/+YHc2E5Q)
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Date: Thu, 03 Apr 1997 17:40:41 -0600
From: Ram <Rao@mayo.edu>
Subject: Re: non-internalizing receptors
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From owner-7tms_r@net.bio.net Mon Apr 07 23:00:00 1997
Path: biosci!mayo.edu!Rao
From: Rao@mayo.edu
Newsgroups: bionet.molbio.proteins.7tms_r
Subject: Re: non-internalizing receptors
Date: 8 Apr 1997 06:48:24 -0700
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--Boundary (ID 1fZrM1JK/L3ySjsQ3JgKpg)
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We have recently reported internalization of CCK receptor by an
antagonist. The paper entitled" Antagonist stimulated internalization
of the G protein coupled CCK receptor appears as a Accelerated
Communication in the March issue of Molecular Pharmacology
Vol:51 Pg 357-362


--Boundary (ID 1fZrM1JK/L3ySjsQ3JgKpg)
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Date: Thu, 03 Apr 1997 17:39:43 -0600
From: Ram <Rao@mayo.edu>
Subject: Re: non-internalizing receptors
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From owner-7tms_r@net.bio.net Mon Apr 07 23:00:00 1997
Path: biosci!mayo.edu!Rao
From: Rao@mayo.edu
Newsgroups: bionet.molbio.proteins.7tms_r
Subject: Re: non-internalizing receptors
Date: 8 Apr 1997 06:01:22 -0700
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--Boundary (ID H70BLRDwMJPZKBMXAbqYCw)
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We have recently reported internalization of CCK receptor by an
antagonist. The paper entitled" Antagonist stimulated internalization
of the G protein coupled CCK receptor appears as a Accelerated
Communication in the March issue of Molecular Pharmacology
Vol:51 Pg 357-362


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Date: Thu, 03 Apr 1997 17:39:18 -0600
From: Ram <Rao@mayo.edu>
Subject: Re: non-internalizing receptors
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From owner-7tms_r@net.bio.net Tue Apr 08 23:00:00 1997
Path: biosci!EMBL-HEIDELBERG.DE!Gert.Vriend
From: Gert.Vriend@EMBL-HEIDELBERG.DE
Newsgroups: bionet.molbio.proteins.7tms_r
Subject: flaming
Date: 9 Apr 1997 08:59:50 -0700
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I suggest this is the last message send to the list about Rao's mail
problem. He apologised for something that probably wasn't even his fault.
That is enough. If not, mail to him, or to me PRIVATELY.
Don't cluther this list. I spend a lot of time chasing people from outside
the GPCR community who deposite garbage (this last set of four porno
adds from last week we traced down to Finland, and the manager of the
system where the dirt came from apologised and promised that repeats
will not happen), and don't want to now also have to get our own
people to look after.

So DONT use 'reply' when you are angry, but send a directed Email.

Gert Vriend

From owner-7tms_r@net.bio.net Tue Apr 08 23:00:00 1997
Path: biosci!bcm.tmc.edu!news.msfc.nasa.gov!news.maxwell.syr.edu!mindspring!cssun.mathcs.emory.edu!news.service.emory.edu!news
From: Kelly Hartline <khartli@emory.edu>
Newsgroups: bionet.molbio.proteins.7tms_r
Subject: Advice on class debate topics
Date: Wed, 09 Apr 1997 10:35:09 -0400
Organization: Emory University School of Medicine
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Hi!

I'm a second year grad student in the neuroscience program at Emory
University, and in my Cell Surface Receptors class, we have two topics
to debate over the next two weeks.

1.  The structure of bacteriorhodopsin is a good model for G
protein-linked receptors.
2.  Transgenic knockouts of receptors do not give more information than
can be obtained 
with selective antagonists.

Specifically, I've been assigned to the 'pro' side for the first topic,
and the 'con' side for the second topic.

I've begun scanning Medline for relevant editorials, reviews, etc., but
I would appreciate any thoughts/opinions that any of you have to offer
on the above subjects.  I would also love to hear of any particular
aspects of the two above issues that you feel would be interesting for
me to examine/focus in on.

Thanks in advance,
Kelly Hartline
(khartli@emory.edu)

From owner-7tms_r@net.bio.net Tue Apr 08 23:00:00 1997
Path: biosci!MED.UNR.EDU!buxton
From: buxton@MED.UNR.EDU ("Iain L. O. Buxton")
Newsgroups: bionet.molbio.proteins.7tms_r
Subject: Re: Sincere apologies
Date: 9 Apr 1997 07:27:24 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
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So Rao, thought you would like to know that in addition to this missive
from you today, I got another, yet different appology copied to me along
with another four of the original banal messages that you keep telling us
you are not responsible for........have a nice day will you, after all,
reading all this RAO RAMMOHAN mail is a great pleasure for us.

PS:  How's the weather in Rochester...?

Iain L. O. Buxton
Professor of Pharmacology/318
Associate Dean for Research
University of Nevada School of Medicine
Howard Medical Sciences Building Rm:216
Reno, NV 89557
Phone:  (702)784-1566
FAX:    (702)784-1620
buxton@med.unr.edu


On 8 Apr 1997, R Rao wrote:

> 
> Dear 7tms_r netters/subscribers,
> 
> With a right and sincere scientific earnest, I posted a mail to the above=
> =20
> newsgroup regarding =D2Antagonist mediated internalization  of a G protein=
> =20
> coupled receptor=D3. Unfortunately the message has been repeating  itself=
> =20
> over and over, resulting  in a flurry of the same message and cluttering=20
> the e-mail of all subscribers.=20
> 
> I realize it is annoying, receiving  similar messages over 20 times but=20
> honestly, it is not a deliberate  attempt in glorifying our publication=20
> or our work.=20
> 
> I notified our institution=D5s Computing facility and after a thorough=20
> check, I was informed that the problem is not from our side. I am told=20
> that somewhere down the line the network went haywire resulting in these=20
> erroneous repeat messages.
> 
> I have informed repeatedly the 7tm newsgroup=D5s help desk and I hope they=
> =20
> are rectifying the problem. Until then, kindly tolerate this barrage of=20
> recurrent  messages.=20
> 
> I also appeal to one and all to desist from sending me abusive letters.=20
> It is unbecoming of Lecturers/Asst Professors/Professors, who write=20
> disdainful letters that carry  crude and raw language.=20
> 
> Finally I hope that this message does not travel the same way as my last on=
> e
> 
> Rao.
> 
> 


From owner-7tms_r@net.bio.net Tue Apr 08 23:00:00 1997
Path: biosci!MED.UNR.EDU!buxton
From: buxton@MED.UNR.EDU ("Iain L. O. Buxton")
Newsgroups: bionet.molbio.proteins.7tms_r
Subject: Re: Sincere apologies
Date: 9 Apr 1997 07:22:52 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 54
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <Pine.WNT.3.95.970409072522.93B-100000@micron.med.unr.edu>
References: <Pine.SOL.3.91.970408160300.18959B-100000@feynman>
NNTP-Posting-Host: net.bio.net

Hey Rao, if you cann't take the heat get out of the kitchen.  You do bot
get to harrass us with your uncontrollable e-mail, blame it on others and
then cry when you're called on it.  Get it!

Iain L. O. Buxton
Professor of Pharmacology/318
Associate Dean for Research
University of Nevada School of Medicine
Howard Medical Sciences Building Rm:216
Reno, NV 89557
Phone:  (702)784-1566
FAX:    (702)784-1620
buxton@med.unr.edu


On 8 Apr 1997, R Rao wrote:

> 
> Dear 7tms_r netters/subscribers,
> 
> With a right and sincere scientific earnest, I posted a mail to the above=
> =20
> newsgroup regarding =D2Antagonist mediated internalization  of a G protein=
> =20
> coupled receptor=D3. Unfortunately the message has been repeating  itself=
> =20
> over and over, resulting  in a flurry of the same message and cluttering=20
> the e-mail of all subscribers.=20
> 
> I realize it is annoying, receiving  similar messages over 20 times but=20
> honestly, it is not a deliberate  attempt in glorifying our publication=20
> or our work.=20
> 
> I notified our institution=D5s Computing facility and after a thorough=20
> check, I was informed that the problem is not from our side. I am told=20
> that somewhere down the line the network went haywire resulting in these=20
> erroneous repeat messages.
> 
> I have informed repeatedly the 7tm newsgroup=D5s help desk and I hope they=
> =20
> are rectifying the problem. Until then, kindly tolerate this barrage of=20
> recurrent  messages.=20
> 
> I also appeal to one and all to desist from sending me abusive letters.=20
> It is unbecoming of Lecturers/Asst Professors/Professors, who write=20
> disdainful letters that carry  crude and raw language.=20
> 
> Finally I hope that this message does not travel the same way as my last on=
> e
> 
> Rao.
> 
> 


From owner-7tms_r@net.bio.net Tue Apr 08 23:00:00 1997
Path: biosci!VIOLET.INCM.U-NANCY.FR!poda
From: poda@VIOLET.INCM.U-NANCY.FR (Gennady PODA)
Newsgroups: bionet.molbio.proteins.7tms_r
Subject: 7tms_r: HIV and opiates, summary
Date: 9 Apr 1997 01:41:08 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 115
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <Pine.SGI.3.91.970409104034.29149A-100000@violet.incm.u-nancy.fr>
NNTP-Posting-Host: net.bio.net



Dear Netters,

One week back, I posted a question about possible interaction of opiates
with chemokine receptor proteins and possible mechanisms of activation of
HIV infection by morphine and other narcotics. 

Here it is the answers. It seems that nobody measured direct binding of 
opiates to chemokine receptors and nobody knows if such kind of interaction 
may or may not take place... 

One of the possible mechanisms could be the influence of opiates on cellular 
immune responses through opioid receptors and cellular signaling systems...

Many thanks for everyone who answered.

Gennady



1 ----------------------------------------------------------------------
Dear Dr. Poda:

I am intrigued with the question you pose.  Faced with a not so disimilar
issue with respect to muscarinic systems and NO synthase inhibitors, we
show that a not-so-high-affinity interaction can be an issue (Buxton, 
I.L.O., Cheek, D.J., Eckman, D.M., Westfall, D.P. Sanders, K.M. and  Keef,
K.D. (1993) NG-nitro-L-arginine methylester (L-NAME) and other alkyl
esters of arginine are muscarinic receptor antagonists. Circ. Res. 72:
387-395.)

We could look at this with you if you are interested?

Iain L. O. Buxton
Professor of Pharmacology/318
Associate Dean for Research
University of Nevada School of Medicine
Howard Medical Sciences Building Rm:216
Reno, NV 89557
Phone:  (702)784-1566
FAX:    (702)784-1620
buxton@med.unr.edu

2 -----------------------------------------------------------------------

One thought I have is effects down-stream of the opiate receptor, and
their influence on cellular immune responses. I wouldn't bet the house
on interactions with CC receptor proteins. An interesting paper to look
at follows, if for any reason because it can serve as an extensively
referenced entry into the literature of how GPCR's linked to adenylyl
cyclase can influence lymphocyte function.

Condie, R., A. Herring, W. S. Koh, M. Lee, and N. E. Kaminski.
Cannabinoid inhibition of adenylate cyclase-mediated signal transduction
and interleukin-2 (IL-2) expression in the murine T-cell line, EL4.IL-2.
J. Biol. Chem. 271(22):13175-13183 (1996).
-- 
T.J. Murphy				404-727-2467
Assistant Professor			404-727-0365 (fax)
Emory University School of Medicine	medtjm@bimcore.emory.edu
Department of Pharmacology		http://www.emory.edu/PHARMACOLOGY/MURPHY/
1510 Clifton Road
Atlanta, GA 30322

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

The question is here:



From poda@violet.incm.u-nancy.frWed Apr  9 10:38:20 1997
Date: 2 Apr 1997 02:00:38 -0800
From: Gennady PODA <poda@violet.incm.u-nancy.fr>
To: 7tms_r@net.bio.net
Subject: 7tms_r: HIV and opiates

Dear Netters,

It is known that morphine and other narcotics alter the function of human
T lymphocytes and monocytes and may lead to activation of HIV infection
(ex., Squinto SP, et al. AIDS Res Hum Retroviruses, 6(10):1163-1168,
1990). Moreover, potentiation of HIV growth by morphine was antagonized by
naloxone and beta-funaltrexamine (opioid antagonists) (Peterson PK, et al.
AIDS 4(9):869-873, 1990). This means that opiate systems involved somehow
in HIV pathogenesis. Did anyone investigate possible mechanisms?

One of the possibilities can be direct binding of opiates to chemokine
receptors (found to be cofactors for HIV and host cell membrane fusion).
So the question, has anyone seen (or measured) binding constants of opiate
ligands (antagonists or agonists) to the chemokine receptors such as
CXCR-4 and CCR-5, etc.? This binding may be rather non specific but even
so... 

Any hints or references would be greatly appreciated. I will summarize 
the answers.

Best wishes and many thanks for your participation,

Gennady




************************************************************
Dr. Gennady PODA

Laboratoire de Chimie theorique (UA 510 du C.N.R.S.)
Universite Henri Poincare, Nancy-I
Faculte des Sciences - Domaine scientifique Victor Grignard
B.P. 239 - 54500 Vandoeuvre-les-Nancy Cedex France

Fax : + 33 (0)3.83.91.25.30   E-mail : poda@incm.u-nancy.fr
************************************************************


From owner-7tms_r@net.bio.net Tue Apr 08 23:00:00 1997
Path: biosci!biochem.umass.edu!bscott
From: bscott@biochem.umass.edu (Brian Scott)
Newsgroups: bionet.molbio.proteins.7tms_r
Subject: Free molecular visualization workshops for profs
Date: 9 Apr 1997 17:49:08 -0700
Organization: University of Massachusetts
Lines: 53
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <334C38C5.37FA@biochem.umass.edu>
Reply-To: bscott@biochem.umass.edu
NNTP-Posting-Host: net.bio.net

Free Workshops on Molecular Visualization
for Undergraduate Bioscience Teaching
Amherst MA -- Summer, 1997-8

Understanding the three-dimensional structures of proteins, DNA,
RNA, and their interactions is difficult from flat pictures, yet
grasping structure is important to understanding function.  Free
software is now available which displays attention-grabbing 3D
animated images of biological molecules in depth-cued spacefilling
color. RasMol (http://www.umass.edu/microbio/rasmol), which
works on Windows or Macs, encourages self-directed exploration.
Chime (http://www.umass.edu/microbio/chime) allows annotated
preset views of molecules to be delivered as web tutorials.

Free, hands-on workshops will be held this summer at the University
of Massachusetts in Amherst to prepare college faculty with no prior
experience to use molecular visualization in their classes.
Participants will travel to the Amherst campus on three separate
days (two this summer, one the following summer), and are
responsible for their own travel expenses (and therefore are
expected primarily from the Northeastern USA). Overnight
accomodations will be provided free to those needing them (based on
distance traveled).  Participants will be expected to incorporate
molecular visualization into their teaching, and to mentor two
faculty colleagues at their home institution.

The workshops will be led by Eric Martz, a Professor in the
Department of Microbiology.  Martz has innovated molecular structure
tutorials which are in use throughout the USA and in dozens of other
countries.  The web site he created (see above) was visited by
40,000 people in 1996.

1997 dates are June 17 and 30 (workshop A), or June 19 and July 2
(workshop B).  Workshops A and B also meet for one day in late June
1998.  To obtain more detailed information and a REGISTRATION
FORM, visit

http://www.umass.edu/microbio/rasmol/workshop.htm

or FAX a request to 413-545-1578,
or email a request to emartz@microbio.umass.edu.

Supported by the National Science Foundation (Undergraduate Faculty
Enhancement, Division of Undergraduate Education) and the University
of Massachusetts.
/* - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - -
Eric Martz, Professor (Immunology), Dept Microbiology, Univ
Massachusetts,
Amherst MA US 01003-5720 413-545-2325 FAX:545-1578.
RasMol Home Page, http://www.umass.edu/microbio/rasmol
Other web projects listed at
http://www.umass.edu/microbio/rasmol/em-web.htm
- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - -*/

From owner-7tms_r@net.bio.net Tue Apr 08 23:00:00 1997
Path: biosci!bcm.tmc.edu!news.msfc.nasa.gov!news.maxwell.syr.edu!news.apfel.de!fu-berlin.de!wuff.mayn.de!wuff.franken.de!winx03!wpxx02!not-for-mail
From: krasel@wpxx02.toxi.uni-wuerzburg.de (Cornelius Krasel)
Newsgroups: bionet.molbio.proteins.7tms_r
Subject: Re: Advice on class debate topics
Date: Wed, 9 Apr 1997 21:20:22 +0200
Organization: University of Wuerzburg, Germany
Lines: 67
Message-ID: <m5qgi5.crs.ln@wpxx02.toxi.uni-wuerzburg.de>
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Kelly Hartline (khartli@emory.edu) wrote:
> Hi!
> 
> I'm a second year grad student in the neuroscience program at Emory
> University, and in my Cell Surface Receptors class, we have two topics
> to debate over the next two weeks.
> 
> 1.  The structure of bacteriorhodopsin is a good model for G
> protein-linked receptors.

Since you have been assigned the "pro" side for this topic, you
should check out articles by Harel Weinstein. I have a few
references for you (there are more, of course):

@article{pardo:92,
        author  = {Leonardo Pardo and Juan Antonio Ballesteros and Roman
                Osman and Harel Weinstein},
        title   = {On the use of the transmembrane domain of bacteriorhodopsin
                as a template for modeling the three-dimensional structure of
                guanine nucleotide-binding regulatory protein-coupled
                receptors.},
        journal = PNAS,
        volume  = 89,
        pages   = {4009--4012},
        year    = 1992
}

@article{dzhang:94,
        author  = {Daqun Zhang and Harel Weinstein},
        title   = {Polarity conserved positions in transmembrane domains
                of {G}-protein coupled receptors and bacteriorhodopsin.},
        journal = FEBS,
        volume  = 337,
        pages   = {207--212},
        year    = 1994
}

Unfortunately it seems that the projection structure of frog rhodopsin
is dissimilar to bacteriorhodopsin. At least that is what Gebhardt
Schertler (who did all these rhodopsin structures) claims. This has
been debated in

@article{hoflack:94,
        author  = {Jan Hoflack and Suzanne Trumpp-Kallmeyer and Marcel
                Hibert},
        title   = {Re-evaluation of bacteriorhodopsin as a model for
                {G} protein-coupled receptors.},
        journal = TIPS,
        volume  = 15,
        pages   = {7--9},
        year    = 1994
}

> 2.  Transgenic knockouts of receptors do not give more information than
> can be obtained with selective antagonists.

The obvious problem is that you have to have selective antagonists,
which you often don't have.

Hope that helps a little,

--Cornelius.

-- 
/* Cornelius Krasel, U Wuerzburg, Dept. of Pharmacology, Versbacher Str. 9 */
/* D-97078 Wuerzburg, Germany   email: phak004@rzbox.uni-wuerzburg.de  SP3 */
/* "Science is the game we play with God to find out what His rules are."  */

From owner-7tms_r@net.bio.net Tue Apr 08 23:00:00 1997
Path: biosci!EMORY.EDU!" smitc04"
From: " smitc04"@EMORY.EDU (stephanie mitchell)
Newsgroups: bionet.molbio.proteins.7tms_r
Subject: Please Help Me
Date: 9 Apr 1997 12:50:45 -0700
Organization: Emory
Lines: 21
Sender: daemon@net.bio.net
Distribution: world
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Hello,

I am a first year graduate student in the pharmacology program at Emory
University  and I have to debate Kelly on the same topics next week.

Topics:

1. The structure of bacteriorhodopsin is not a good model for G- protein
linked receptors.

2. Transgenic knockouts of receptors do give more information than can
be obtained with selective antagonists.

If you agree with the above topics and can send me any information to
support them I would appreciate it.

I have started a net  search and have found very  little information to
support topic #1.

Thanks in advance,
Stephanie Mitchell

From owner-7tms_r@net.bio.net Wed Apr 09 23:00:00 1997
Path: biosci!agate!howland.erols.net!europa.clark.net!newsfeed.nacamar.de!wuff.mayn.de!wuff.franken.de!winx03!wpxx02!not-for-mail
From: krasel@wpxx02.toxi.uni-wuerzburg.de (Cornelius Krasel)
Newsgroups: bionet.molbio.proteins.7tms_r
Subject: Re: Advice on class debate topics
Date: Thu, 10 Apr 1997 09:56:26 +0200
Organization: University of Wuerzburg, Germany
Lines: 21
Message-ID: <af6ii5.73u.ln@wpxx02.toxi.uni-wuerzburg.de>
References: <334BA91D.7099@emory.edu> <m5qgi5.crs.ln@wpxx02.toxi.uni-wuerzburg.de>
NNTP-Posting-Host: wpxx02.toxi.uni-wuerzburg.de
X-Newsreader: TIN [UNIX 1.3 950824BETA PL0]

Dan Strahs has alerted me that the second Weinstein paper I quoted,

> @article{dzhang:94,
>         author  = {Daqun Zhang and Harel Weinstein},
>         title   = {Polarity conserved positions in transmembrane domains
>                 of {G}-protein coupled receptors and bacteriorhodopsin.},
>         journal = FEBS,
>         volume  = 337,
>         pages   = {207--212},
>         year    = 1994
> }

actually argues against a similarity between bacteriorhodopsin and
the GPCRs. I apologize. (Never quote a paper from memory...)

--Cornelius.

-- 
/* Cornelius Krasel, U Wuerzburg, Dept. of Pharmacology, Versbacher Str. 9 */
/* D-97078 Wuerzburg, Germany   email: phak004@rzbox.uni-wuerzburg.de  SP3 */
/* "Science is the game we play with God to find out what His rules are."  */

From owner-7tms_r@net.bio.net Thu Apr 10 23:00:00 1997
Path: biosci!INKA.MSSM.EDU!hweinstein
From: hweinstein@INKA.MSSM.EDU (Dr. Harel Weinstein)
Newsgroups: bionet.molbio.proteins.7tms_r
Subject: (none)
Date: 11 Apr 1997 21:45:27 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 64
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <v01540b03af74bc3b2226@[146.203.3.14]>
NNTP-Posting-Host: net.bio.net

Dear Colleagues,
There seems to have been some confusion about the treatment given in our
publications to the use of Bacteriorhodopsin as a template for GPCRs. I
would like to offer a clarification of our current understanding, as it
continue to be consistent with all the previous considerations.
The two articles mentioned in recent correspondence here, i.e., Pardo et
al, PNAS 1992, and Zhang & Weinsten, FEBS Letters, 1994 provide different
types of data to support the same clear, and by now unassailable assertion
that bacteriorhodopsin IS NOT a suitable structural model for  the assembly
of the 7 TMH bundle of GPCRs. The main, and conceptually quite
straightforward reason is that the important differences in the amino acid
sequences of BR and the GPCRs preclude a similarity in the bundling of the
seven transmembrane helices in a pattern that could be similar in the two
DIFFERENT families of membrane proteins (not that low homology per se is
not a definitive criterion for lack of structural similarity, as many
examples now exist of such cases, but if clearly defined differences can be
shown to be responsible for divergent properties, then the lack of sequence
homology can be expected safely to be accompanied by lack of structural
homology). The main elements of the dissimilar sequence that are
responsible for the difference in bundling center on the distribution of
Proline residues among the TMHs in the two families, and the effect of the
significant difference in the positions of the Pro even in the helices in
which they appear in both Families. These issues are discussed in depth,
with explicit and quantitative detail in the comprehensive review chapter
we published (Ballesteros & Weinstein, Methods in Neurosciences Vol 25,
(Ed. S.C. Sealfon) pp. 366-428, 1995.). The capital importance of the Pro
for the structure of the TMHs, and their ability to interact in the bundle
has been demonstrated experimentally in relation to the rhodopsin-based
models, in a recent publication (Fu et al, Biochemistry,   35:11278-11285,
1996). The effect of the Pro-kink (or the more complex distortion produced
by an Asn-Pro or Asp/Pro sequence) on a TMH, which is clearly demonstrated
by the experimental results, also clarifies the often encountered confusion
produced by the use of ideal alpha-helices in models of GPCR TMH bundles
(e.g., the erroneous "inability" of such inadequate ideal models to account
for a number of experimentally observed helix-helix interactions, such as
the TMH2-TMH7 interaction described in Zhou et al, Mol. Pharmacol.
45:165-170,1994 and Sealfon et al, J. Biol. Chem. 270:16683-16688,  1995).
The inappropriate use of ideal alpha-helices in Pro-containing helices of
models of the TMH bundle, regardless of the manner in which the individual
helices and their orientations (i.e., lipid face vs. interior face) were
determined, seems to have lead to strange and misleading conclusions. Given
the conceptual inadequacy of such simplistic helix constructs, and the
clear experimental evidence against them, it seems to us in this Lab, that
their continued use is unadvisable.
I hope this is useful and that it may generate some good discussion.
Best regards to all,
HW



----------------------------------------------------------------------------
----------------------------------
Dr. Harel Weinstein
Professor and Chairman
Department of Physiology and Biophysics
Box 1218
Mount Sinai School of Medicine
New York, NY 10029-6574
(212) 241-7018
Fax 212 860 3369

WW Web Page   http://www.mssm.edu/physbio/local/primfac/weinstein.html



From owner-7tms_r@net.bio.net Fri Apr 11 23:00:00 1997
Path: biosci!internet!biosci!not-for-mail
From: biohelp (BIOSCI Administrator)
Newsgroups: bionet.molbio.proteins.7tms_r
Subject: BIOSCI/bionet miniFAQ & Fundraiser
Date: 12 Apr 1997 02:00:12 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 239
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <199704120900.CAA09644@net.bio.net>
NNTP-Posting-Host: net.bio.net

(LAST REVISION: 30-JUL-95)

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

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

		       biosci-help@net.bio.net

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


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

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

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

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

	4) The BIOSCI user address and research interest directory.


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

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

First, please use our WWW system at http://www.bio.net/ to access the
archives.  You can post or reply to messages via your Web browser as
described in item #1 below.  Your usage helps attract sponsors. If you
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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
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tech support address, biosci-help@net.bio.net.


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


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

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

What can BIOSCI/bionet do to protect its newsgroups?
----------------------------------------------------
The only solution currently available is to moderate the newsgroup.
If this newsgroup is already moderated, then you are in good shape.
Moderation protects the USENET distribution from about 95% of the
spams that are being sent to date and protects the mailing lists
completely.  Moderation means, however, that someone has to take the
time to review each message before it goes out.  We have set up
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This takes no more time than that needed to read the message and pass
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Most newsgroups currently have a discussion leader who is responsible
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hit with too many junk postings, please contact the discussion leader
for that group and see if there is interest in moderating the group.
Please do not assume that by simply posting a complaint to the
newsgroup itself, anyone on the BIOSCI staff will act on your
complaint.  With close to 100 newsgroups to run, the BIOSCI staff has
to rely on the discussion leaders of each newsgroup to report problems
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We will moderate any of our newsgroups if the discussion leader tells
us that the readership of the group wishes to do so and if a moderator
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entails only a few minutes of work each day.

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


3) Examples of subscribing and unsubscribing to the mailing lists.
------------------------------------------------------------------
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Gory details are in the BIOSCI Information sheets on the Web at
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METHODS-AND-REAGENTS list at both of our two BIOSCI sites:

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

A) Determine the "listname" which is the <=8 character mail address
                                         ^^^^^^^^^^^^^
   for the group.  These can be found in the BIOSCI Info. Sheet.  For
   the METHODS-AND-REAGENTS group the mailing address is
   methods@net.bio.net.  The listname is the portion of the address to
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Users in Europe, Africa, and Central Asia who use the BIOSCI node at
--------------------------------------------------------------------
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-------------------------------------------------

To subscribe and unsubscribe to/from the BIOSCI lists, you need to
specify the full USENET newsgroup name with "bionet-news." prepended.
The USENET newsgroup names are listed in the BIOSCI Information sheet
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These commands are included in a message addressed to mxt@dl.ac.uk,
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To unsubscribe from all the lists at the UK node, use

    unsub bionet-news

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

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

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

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

				Sincerely,

				Dave Kristofferson
				BIOSCI/bionet Manager

				biosci-help@net.bio.net

From owner-7tms_r@net.bio.net Fri Apr 11 23:00:00 1997
Path: biosci!BIOCSERVER.BIOC.CWRU.EDU!roth
From: roth@BIOCSERVER.BIOC.CWRU.EDU
Newsgroups: bionet.molbio.proteins.7tms_r
Subject: Re: proline kinks
Date: 12 Apr 1997 07:14:28 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 52
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <199704121415.OAA13811@biocserver.BIOC.CWRU.Edu>
NNTP-Posting-Host: net.bio.net

Harel Weinstein recently stated that:

"The capital importance of the Pro for the structure of the TMHs, and their 
ability to interact in the bundle
has been demonstrated experimentally in relation to the rhodopsin-based
models, in a recent publication (Fu et al, Biochemistry,   35:11278-11285,
1996)."

>From the outset, I'd like to say that I do agree with the general 
conclusions of the Fu et al article and that we have data (submitted) that 
agrees with the general orientation of residues in Helix VII and that this 
new insight certainly clarifies some important experimental findings which 
were confusing.  

Thus said, it should be emphasized that the Fu article, although elegant in 
design and interpretation, really gives no direct evidence for the model 
proposed.  The study is essentially a cys-substitution accessibility study 
in which hydrophilic cysteine reagents are used to inhibit ligand binding. 
This study proposes, based on unexpected findings, that there is a 
pronounced 'kink' introduced by a Pro in Helix VII.  

A rather trivial interpretation for  the results is that cys-substitution 
non-specifically alters helical packing and/or accessibility. Without 
detailed structural studies of the type which are currently unavailable it 
will be difficult to rule out many of these types of artifacts which can 
confound the interpretation of the data.

What is important about the Fu et al study is that it gives a plausible 
model to account for some unexpected findings.  I think its a bit premature, 
however, to argue that these results *directly* support the notion that Pro 
kinks actually occur in 7-TM receptors.  

What I believe all of this reinforces, though, is the necessity for 
structural studies of 7-TM receptors.

Bryan Roth
=============================================================

Bryan L.Roth MD, PhD
Associate Professor                 
Departments of Psychiatry, Biochemistry and Neurosciences    
Room W438
Case Western Reserve University Medical School
10900 Euclid Avenue
Cleveland, OH 44106-4935

216-368-4544 (Fax)
216-368-2730 (Office)
roth@biocserver.cwru.edu

web page:  http://www.cwru.edu/CWRU/Dept/Med/biochemistry/faculty/roth.html


From owner-7tms_r@net.bio.net Mon Apr 14 23:00:00 1997
Path: biosci!SHOWME.MISSOURI.EDU!c680296
From: c680296@SHOWME.MISSOURI.EDU
Newsgroups: bionet.molbio.proteins.7tms_r
Subject: (none)
Date: 15 Apr 1997 09:28:53 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 2
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <Pine.A41.3.95q.970415112752.146804A-100000@sp2n09.missouri.edu>
NNTP-Posting-Host: net.bio.net

SUBSCRIBE


From owner-7tms_r@net.bio.net Mon Apr 14 23:00:00 1997
Path: biosci!SHOWME.MISSOURI.EDU!c680296
From: c680296@SHOWME.MISSOURI.EDU ("David M. Bourdon")
Newsgroups: bionet.molbio.proteins.7tms_r
Subject: serotonin receptor newsgroup?
Date: 15 Apr 1997 20:02:45 -0700
Organization: Dept. of Pharmacology - MU School of Medicine
Lines: 11
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <33545EC6.257A@showme.missouri.edu>
NNTP-Posting-Host: net.bio.net

Does anyone know of a serotonin receptor newsgroup on the internet?  I'm studying 5-HT 
GPCR subtypes in peripheral tissues of the rat.      
-- 
DAVID M. BOURDON -- Contact Information

Graduate Research Assistant
Department of Pharmacology, M517B Med.Sci.Bldg.
MU School of Medicine, Columbia, MO  65212 USA
phone:  573-882-1554
fax:  573-884-4558
home page: http://www.missouri.edu/~c680296/index.html

From owner-7tms_r@net.bio.net Tue Apr 15 23:00:00 1997
Path: biosci!news.ohsu.edu!NewsWatcher!user
From: forte@ohsu.edu (Michael Forte)
Newsgroups: bionet.molbio.proteins.7tms_r
Subject: CHO Cells
Date: 16 Apr 1997 21:43:33 GMT
Organization: Vollum Institute
Lines: 7
Message-ID: <forte-1604971439380001@137.53.98.58>
NNTP-Posting-Host: 137.53.98.58

Hi,

I know this issue has been raised in this group before, but of course I
didn't care then.  Can anyone tell me or point me to a reference
concerning the spectrum of Galpha proteins expressed in CHO cells. Thanks.

Mike Forte

From owner-7tms_r@net.bio.net Wed Apr 16 23:00:00 1997
Path: biosci!daresbury!uninett.no!news-feed.inet.tele.dk!newsfeed.nacamar.de!fu-berlin.de!news-ber1.dfn.de!news-ham1.dfn.de!news-han1.dfn.de!news-koe1.dfn.de!news.ruhr-uni-bochum.de!news.rhrz.uni-bonn.de!usenet
From: R.B.Jansen@Uni-Bonn.de (Raymond "ElRay" B. Jansen)
Newsgroups: bionet.molbio.proteins.7tms_r
Subject: preotein sequencing..............urgent!
Date: Thu, 17 Apr 1997 11:16:09 GMT
Organization: Universitaet Bonn, Botanisches Institut
Lines: 17
Message-ID: <33560666.11731026@news.rhrz.uni-bonn.de>
NNTP-Posting-Host: rhrz-ts1-p12.rhrz.uni-bonn.de
X-Newsreader: Forte Free Agent 1.1/32.230

Dear colleagues,

I am desperately looking for a quick and reasonable opportunity to
sequence my purified proteins.
These proteins are bound to a PVDF-membrane, so, that they can 
cut off easily  for sequencing.

What I want to know exactly is, who (maybe a company) is able to do
the job for me and what will be the price for this.

If there is someone out and know the answers please contact me by
e-mail.My address is: unb13c@ibm.rhrz.uni-bonn.de.

I appreciate every help.

Thanks in advance,
  Mechthild

From owner-7tms_r@net.bio.net Wed Apr 16 23:00:00 1997
Path: biosci!daresbury!uninett.no!news-feed.inet.tele.dk!cpk-news-hub1.bbnplanet.com!news.bbnplanet.com!ais.net!uunet!in3.uu.net!192.108.254.3!news.teleport.com!not-for-mail
From: nevek@teleport.com (Kim Neve)
Newsgroups: bionet.molbio.proteins.7tms_r
Subject: how to subscribe/unsubscribe
Date: Thu, 17 Apr 1997 15:21:48 GMT
Organization: Oregon Health Sciences University
Lines: 163
Message-ID: <33563f63.257251928@news.teleport.com>
NNTP-Posting-Host: ip-pdx10-12.teleport.com
X-Newsreader: Forte Free Agent 1.1/32.230

I have seen a number of futile subscribe/unsubscribe messages in this
newsgroup recently, so perhaps it is time to re-post the instructions.
The following is a message posted by Rick Neubig a year ago.
_______________________________________________

You need to unsubscribe yourself. Here's some info about the 
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_________________________________________________________
Rick Neubig                             RNeubig@umich.edu
University of Michigan               Phone (313) 763-3650
http://www.umich.edu/~rneubig        FAX   (313) 763-4450


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From owner-7tms_r@net.bio.net Thu Apr 17 23:00:00 1997
Path: biosci!bcm.tmc.edu!news.msfc.nasa.gov!europa.clark.net!cpk-news-hub1.bbnplanet.com!news.bbnplanet.com!news-peer.sprintlink.net!news.sprintlink.net!sprint!howland.erols.net!newsxfer.itd.umich.edu!news.mtu.edu!msunews!netnews.upenn.edu!brass6.med.upenn.edu!user
From: obrien@pharm.med.upenn.edu (:-Peter)
Newsgroups: bionet.molbio.proteins.7tms_r
Subject: Re: CHO Cells
Date: 18 Apr 1997 14:59:03 GMT
Organization: U. of Pennsylvania
Lines: 26
Message-ID: <obrien-1804971106380001@brass6.med.upenn.edu>
References: <forte-1604971439380001@137.53.98.58>
NNTP-Posting-Host: brass6.med.upenn.edu

In article <forte-1604971439380001@137.53.98.58>, forte@ohsu.edu (Michael
Forte) wrote:

@ Hi,
@ 
@ I know this issue has been raised in this group before, but of course I
@ didn't care then.  Can anyone tell me or point me to a reference
@ concerning the spectrum of Galpha proteins expressed in CHO cells. Thanks.
@ 
@ Mike Forte

Mike, 

A useful tool for looking up old usenet posts is called Dejanews.  Point
your web browser to http://www.dejanews.com/

One can search for previously posted articles using keywords, group names
etc.  It cuts down on the reiteration of topics that have been covered in
the past, thus saving a bit of that mythical, precious "bandwidth."

:-Peter  






From owner-7tms_r@net.bio.net Fri Apr 18 23:00:00 1997
Path: biosci!EMORY.EDU!hawad
From: hawad@EMORY.EDU (Hazar  Awad)
Newsgroups: bionet.molbio.proteins.7tms_r
Subject: Transgenic KO's vs. selective antagonists.
Date: 19 Apr 1997 08:34:46 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 13
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <Pine.GSO.3.95.970419112856.4209A-100000@curly.cc.emory.edu>
NNTP-Posting-Host: net.bio.net


Hi.  I am a first year graduate student in the pharmacology program at
Emory University.  I have been assigned the following debate topic for my
Cell Surface Receptors class:

-Transgenic knockouts of receptors do not give more information than can
be obtained with selective antagonists.

Any thoughts on this topic would be greatly appreciated.

Hazar Awad.
hawad@emory.edu


From owner-7tms_r@net.bio.net Sat Apr 19 23:00:00 1997
Path: biosci!ihnp4.ucsd.edu!munnari.OZ.AU!news.ecn.uoknor.edu!feed1.news.erols.com!news-xfer.netaxs.com!cronkite.ocis.temple.edu!astro.temple.edu!not-for-mail
From: driska@astro.temple.edu (Stephen P. Driska PhD)
Newsgroups: bionet.molbio.proteins.7tms_r
Subject: Re: non-internalizing receptors
Date: 17 Apr 1997 19:48:54 GMT
Organization: Temple University, Academic Computer Services
Lines: 32
Distribution: world
Message-ID: <5j5ur6$j7f@cronkite.ocis.temple.edu>
References: <01IHEZBSS1XM000042@mc.duke.edu>
NNTP-Posting-Host: astro.ocis.temple.edu
NNTP-Posting-User: 536870664
X-Newsreader: TIN [UNIX 1.3 950824BETA PL0]


Rao@mayo.edu wrote:

	16 times! that ....

: We have recently reported internalization of CCK receptor by an
: antagonist. The paper entitled" Antagonist stimulated internalization
: of the G protein coupled CCK receptor appears as a Accelerated
: Communication in the March issue of Molecular Pharmacology
: Vol:51 Pg 357-362
: 


	What causes these repeat messages?  Is it someone posting from a 
newsreader like tin, not seeing the posting immediately, and repeatedly 
trying to post again?

	Some advice if this is the problem:  

	If you're using tin to read the news, you may need to leave the 
newsgroup and then re-enter it before your post will be shown....

	Just an idea......

		Steve



-- 
Steve Driska, Physiology Department, Temple University Medical School
Philadelphia, PA 19140 USA                  (215) 707-3283 
driska@astro.ocis.temple.edu  


From owner-7tms_r@net.bio.net Sat Apr 19 23:00:00 1997
Path: biosci!daresbury!not-for-mail
From: Alessandro Giolitti <lns@dada.it>
Newsgroups: bionet.molbio.proteins.7tms_r
Subject: Paper on Bradykinin receptor purification
Date: 21 Apr 1997 06:39:19 +0100
Lines: 27
Sender: lpddist@mserv1.dl.ac.uk
Distribution: bionet
Message-ID: <5jeui8$q2l@mserv1.dl.ac.uk>
X-Sender: lns@mail.dada.it
Original-To: 7tms_r@dl.ac.uk

Dear netters,

 I have only recently  found the paper by M. Yaqoo and C.R.Snell
"Purification and Characterization of B2 Bradykinin Receptor from Rat
Uterus", on J. Neurochem. 1994, 62(1), 17-26. I was wondering what is the
opinion other people has about this work. Since it seems that the
solubilized receptor mantains most of the binding ability for bradykinin
and antagonists, and a high specificity, it looks like it is also
mantaining its tertiary structure. What do the 7tm community thinks about?

Thanks,


Alessandro Giolitti

____________________________________________________________

   Dr. Alessandro Giolitti
   Drug Design Dept.                  Ph.   : +39-55-5680240
   Menarini Ricerche S.p.A.           FAX   : +39-55-5680419
   Via Sette Santi, 3		                 e-mail: lns@dada.it
   50131 Firenze
   Italy

____________________________________________________________



From owner-7tms_r@net.bio.net Tue Apr 22 23:00:00 1997
Path: biosci!bcm.tmc.edu!news.msfc.nasa.gov!news-spur1.maxwell.syr.edu!news.maxwell.syr.edu!newsxfer3.itd.umich.edu!newsxfer.itd.umich.edu!nntp.cs.ubc.ca!psgrain!news.rain.net!atheria.europa.com!isdn4.europa.com!user
From: paulw@nwneuro.com
Newsgroups: bionet.molbio.proteins.7tms_r
Subject: Combinatorial library determination
Date: 23 Apr 97 20:00:13 GMT
Organization: Europa Communications Inc. [Portland, OR]
Lines: 3
Message-ID: <paulw-2304971302070001@isdn4.europa.com>
NNTP-Posting-Host: atheria.europa.com

Does anyone have a source of information to determine which types of
combinatorial libraries are more likely to interact with g-protein linked
receptors?

From owner-7tms_r@net.bio.net Wed Apr 23 23:00:00 1997
Path: biosci!pr.cyanamid.com!ramaswam
From: ramaswam@pr.cyanamid.com (Ramaswamy Nilakantam)
Newsgroups: bionet.molbio.proteins.7tms_r
Subject: combinatorial library
Date: 24 Apr 1997 08:56:20 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 13
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <199704241555.AA149707308@primail.pr.cyanamid.com>
NNTP-Posting-Host: net.bio.net

paulw wrote:
Does anyone have a source of information to determine which types of
combinatorial libraries are more likely to interact with g-protein linked
receptors?

You might try a small company called Pharmacopeia, in Princeton, NJ. They are
in the business of designing combinatorial libraries. You might be able to
get the info' you are looking for from someone there without actually buying
anything. Worth a try anyway. 

Ramaswamy Nilakantan
Wyeth-Ayerst Research
Pearl River, NY

From owner-7tms_r@net.bio.net Sun Apr 27 23:00:00 1997
Path: biosci!FARMR1.MED.UTH.TMC.EDU!aschonb
From: aschonb@FARMR1.MED.UTH.TMC.EDU ("A. Schonbrunn")
Newsgroups: bionet.molbio.proteins.7tms_r
Subject: endogenous receptors
Date: 28 Apr 1997 15:32:32 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 24
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <v03007802af8ad6539436@[129.106.28.19]>
NNTP-Posting-Host: net.bio.net

I periodically continue to receive requests for the list of receptors
expressed in cells commonly used in transfection studies and have now
posted my most recent compillation at:

http://www.biomedcomp.com/GPCR.html

I will continue to update this list, so please send additions & corrections
directly to me and I will make the necessary modifications.

Thanks to everyone who provided input - your name should be listed on the
web page:  again let me know if I've inadvertantly omitted someone.

as



**************************************************************************
Agnes Schonbrunn, Ph.D.            e-mail: aschonb@farmr1.med.uth.tmc.edu
Professor                          FAX:  713-500-7456
Dept of Integrative Biology, Pharmacology & Physiology
Univ. of Texas Medical School
P.O.Box 20708, Houston,TX 77225



From owner-7tms_r@net.bio.net Mon Apr 28 23:00:00 1997
Path: biosci!niob.knaw.nl!domain
From: domain@niob.knaw.nl
Newsgroups: bionet.molbio.proteins.7tms_r
Subject: changed domain
Date: 29 Apr 1997 00:22:26 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 21
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <199704290722.AAA10839@net.bio.net>
NNTP-Posting-Host: net.bio.net

This is an automatic generated message !

Our email and WWW address has changed from :

                xxxxx@hubrecht.nl      and     www.hubrecht.nl

to
                xxxxx@niob.knaw.nl     and     www.niob.knaw.nl


e.g.            jane@hubrecht.nl 
    is  now     jane@niob.knaw.nl


don't use hubrecht.nl or hl99.hubrecht.nl anymore


--------------------------------------------------------------------------------
NIOB uppsalalaan 8, 3584CT Utrecht The Netherlands, ( Hubrecht laboratory )
EMAIL postmaster@niob.knaw.nl 
--------------------------------------------------------------------------------

From owner-7tms_r@net.bio.net Tue Apr 29 23:00:00 1997
Path: biosci!NEWSSUN.MED.MIAMI.EDU!idickers
From: idickers@NEWSSUN.MED.MIAMI.EDU (Ian Dickerson)
Newsgroups: bionet.molbio.proteins.7tms_r
Subject: subscribe
Date: 30 Apr 1997 13:09:48 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 7
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <v01540b04af8d662b97d5@[129.171.129.155]>
NNTP-Posting-Host: net.bio.net

How do I subscribe?

Thanks,

ian Dickerson



From owner-7tms_r@net.bio.net Wed Apr 30 23:00:00 1997
Path: biosci!BIOCSERVER.BIOC.CWRU.EDU!roth
From: roth@BIOCSERVER.BIOC.CWRU.EDU
Newsgroups: bionet.molbio.proteins.7tms_r
Subject: Position available
Date: 1 May 1997 06:26:16 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 31
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <199705011327.NAA09462@biocserver.BIOC.CWRU.Edu>
NNTP-Posting-Host: net.bio.net

A postdoctoral fellow position will be available in September in the 
Department of Biochemistry at Case Western Reserve University Medical School 
to study structure-activity relationships with 5-HT2-family receptors, 
Gq-like proteins and RGS proteins.  Experience with protein purification is 
essential and expertise with baculovirus expression systems is desirable.  

The position is for two years with a posibility of a one- or two-year 
extension. Salary is negotiable and dependent upon qualifications.

For further information contact Dr. Bryan Roth at the address below.  More 
information may be obtained at the Web page: 

http://www.cwru.edu/CWRU/Dept/Med/biochemistry/faculty/roth.html

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

Bryan L.Roth MD, PhD
Associate Professor                 
Departments of Psychiatry, Biochemistry and Neurosciences    
Room W438
Case Western Reserve University Medical School
10900 Euclid Avenue
Cleveland, OH 44106-4935

216-368-4544 (Fax)
216-368-2730 (Office)
roth@biocserver.cwru.edu

web page:  http://www.cwru.edu/CWRU/Dept/Med/biochemistry/faculty/roth.html


From owner-7tms_r@net.bio.net Wed Apr 30 23:00:00 1997
Path: biosci!UCHICAGO.EDU!g-bell
From: g-bell@UCHICAGO.EDU (Graeme Bell)
Newsgroups: bionet.molbio.proteins.7tms_r
Subject: (none)
Date: 1 May 1997 06:42:59 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 3
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <v01530504af8e5cd293de@[128.135.170.57]>
NNTP-Posting-Host: net.bio.net

unsubscribe



From owner-7tms_r@net.bio.net Wed Apr 30 23:00:00 1997
Path: biosci!WPMAIL.PAISLEY.AC.UK!samb-bs0
From: samb-bs0@WPMAIL.PAISLEY.AC.UK (Balwinder Sambi)
Newsgroups: bionet.molbio.proteins.7tms_r
Subject: GPCRs
Date: 1 May 1997 02:27:15 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 7
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <s36870f6.084@wpmail.paisley.ac.uk>
NNTP-Posting-Host: net.bio.net

Does anyone know what endogenous