Loading…

The identification of ligands at orphan G-protein coupled receptors

The completion of the human genome sequencing project has identified approximately 720 genes that belong to the G-protein coupled receptor (GPCR) superfamily. Approximately half of these genes are thought to encode sensory receptors. Of the remaining 360 receptors, the natural ligand has been identi...

Full description

Saved in:
Bibliographic Details
Published in:Annual review of pharmacology and toxicology 2004-01, Vol.44 (1), p.43-66
Main Authors: WISE, Alan, JUPE, Steven C, REES, Stephen
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c425t-7d675c189342abb42bc8b7229b213afac7331fd967a2b12969e403e9ec66a75b3
cites cdi_FETCH-LOGICAL-c425t-7d675c189342abb42bc8b7229b213afac7331fd967a2b12969e403e9ec66a75b3
container_end_page 66
container_issue 1
container_start_page 43
container_title Annual review of pharmacology and toxicology
container_volume 44
creator WISE, Alan
JUPE, Steven C
REES, Stephen
description The completion of the human genome sequencing project has identified approximately 720 genes that belong to the G-protein coupled receptor (GPCR) superfamily. Approximately half of these genes are thought to encode sensory receptors. Of the remaining 360 receptors, the natural ligand has been identified for approximately 210 receptors, leaving 150 so-called orphan GPCRs with no known ligand or function. The identification of ligands active at orphan GPCRs has been achieved through the development of a number of experimental approaches, including the screening of putative small molecule and peptide ligands, reverse pharmacology, and the use of bioinformatics to predict candidate ligands. In this review, we discuss the methodologies developed for the identification of ligands at orphan GPCRs and include examples of their successful application.
doi_str_mv 10.1146/annurev.pharmtox.44.101802.121419
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_80123212</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>80123212</sourcerecordid><originalsourceid>FETCH-LOGICAL-c425t-7d675c189342abb42bc8b7229b213afac7331fd967a2b12969e403e9ec66a75b3</originalsourceid><addsrcrecordid>eNpFkE1LxDAURYMozjj6F6QbBRetecnr13IYdBQG3IzrkKapE-kkNWlF_72VVlw83uZw7-UQcgc0AcDsXlo7eP2ZdAfpj737ShAToFBQlgADhPKELCHFNEZO8ZQsKc9YDBmyBbkI4Z1SWnKEc7IAzBEZL5Zksz_oyNTa9qYxSvbG2cg1UWvepK1DJPvI-bHORtu4867XxkbKDV2r68hrpbve-XBJzhrZBn01_xV5fXzYb57i3cv2ebPexQpZ2sd5neWpgmLcwGRVIatUUeWMlRUDLhupcs6hqcssl6wCVmalRsp1qVWWyTyt-IrcTrnjko9Bh14cTVC6baXVbgiioMA4G29F1hOovAvB60Z03hyl_xZAxa9JMZsUfyYFophMisnkmHE9lw3VUdf_CbO6EbiZARmUbBsvrTLhn0tTxmkK_Ac2f4Jf</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>80123212</pqid></control><display><type>article</type><title>The identification of ligands at orphan G-protein coupled receptors</title><source>Annual Reviews</source><creator>WISE, Alan ; JUPE, Steven C ; REES, Stephen</creator><creatorcontrib>WISE, Alan ; JUPE, Steven C ; REES, Stephen</creatorcontrib><description>The completion of the human genome sequencing project has identified approximately 720 genes that belong to the G-protein coupled receptor (GPCR) superfamily. Approximately half of these genes are thought to encode sensory receptors. Of the remaining 360 receptors, the natural ligand has been identified for approximately 210 receptors, leaving 150 so-called orphan GPCRs with no known ligand or function. The identification of ligands active at orphan GPCRs has been achieved through the development of a number of experimental approaches, including the screening of putative small molecule and peptide ligands, reverse pharmacology, and the use of bioinformatics to predict candidate ligands. In this review, we discuss the methodologies developed for the identification of ligands at orphan GPCRs and include examples of their successful application.</description><identifier>ISSN: 0362-1642</identifier><identifier>EISSN: 1545-4304</identifier><identifier>DOI: 10.1146/annurev.pharmtox.44.101802.121419</identifier><identifier>PMID: 14744238</identifier><language>eng</language><publisher>Palo Alto, CA: Annual Reviews</publisher><subject>Biological and medical sciences ; Cell receptors ; Cell structures and functions ; Fundamental and applied biological sciences. Psychology ; Humans ; Ligands ; Miscellaneous ; Molecular and cellular biology ; Receptors, G-Protein-Coupled - biosynthesis ; Receptors, G-Protein-Coupled - physiology ; Receptors, Nicotinic - metabolism ; Sequence Homology, Amino Acid ; Transfection</subject><ispartof>Annual review of pharmacology and toxicology, 2004-01, Vol.44 (1), p.43-66</ispartof><rights>2004 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c425t-7d675c189342abb42bc8b7229b213afac7331fd967a2b12969e403e9ec66a75b3</citedby><cites>FETCH-LOGICAL-c425t-7d675c189342abb42bc8b7229b213afac7331fd967a2b12969e403e9ec66a75b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,4182,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=15523051$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/14744238$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>WISE, Alan</creatorcontrib><creatorcontrib>JUPE, Steven C</creatorcontrib><creatorcontrib>REES, Stephen</creatorcontrib><title>The identification of ligands at orphan G-protein coupled receptors</title><title>Annual review of pharmacology and toxicology</title><addtitle>Annu Rev Pharmacol Toxicol</addtitle><description>The completion of the human genome sequencing project has identified approximately 720 genes that belong to the G-protein coupled receptor (GPCR) superfamily. Approximately half of these genes are thought to encode sensory receptors. Of the remaining 360 receptors, the natural ligand has been identified for approximately 210 receptors, leaving 150 so-called orphan GPCRs with no known ligand or function. The identification of ligands active at orphan GPCRs has been achieved through the development of a number of experimental approaches, including the screening of putative small molecule and peptide ligands, reverse pharmacology, and the use of bioinformatics to predict candidate ligands. In this review, we discuss the methodologies developed for the identification of ligands at orphan GPCRs and include examples of their successful application.</description><subject>Biological and medical sciences</subject><subject>Cell receptors</subject><subject>Cell structures and functions</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Humans</subject><subject>Ligands</subject><subject>Miscellaneous</subject><subject>Molecular and cellular biology</subject><subject>Receptors, G-Protein-Coupled - biosynthesis</subject><subject>Receptors, G-Protein-Coupled - physiology</subject><subject>Receptors, Nicotinic - metabolism</subject><subject>Sequence Homology, Amino Acid</subject><subject>Transfection</subject><issn>0362-1642</issn><issn>1545-4304</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><recordid>eNpFkE1LxDAURYMozjj6F6QbBRetecnr13IYdBQG3IzrkKapE-kkNWlF_72VVlw83uZw7-UQcgc0AcDsXlo7eP2ZdAfpj737ShAToFBQlgADhPKELCHFNEZO8ZQsKc9YDBmyBbkI4Z1SWnKEc7IAzBEZL5Zksz_oyNTa9qYxSvbG2cg1UWvepK1DJPvI-bHORtu4867XxkbKDV2r68hrpbve-XBJzhrZBn01_xV5fXzYb57i3cv2ebPexQpZ2sd5neWpgmLcwGRVIatUUeWMlRUDLhupcs6hqcssl6wCVmalRsp1qVWWyTyt-IrcTrnjko9Bh14cTVC6baXVbgiioMA4G29F1hOovAvB60Z03hyl_xZAxa9JMZsUfyYFophMisnkmHE9lw3VUdf_CbO6EbiZARmUbBsvrTLhn0tTxmkK_Ac2f4Jf</recordid><startdate>20040101</startdate><enddate>20040101</enddate><creator>WISE, Alan</creator><creator>JUPE, Steven C</creator><creator>REES, Stephen</creator><general>Annual Reviews</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20040101</creationdate><title>The identification of ligands at orphan G-protein coupled receptors</title><author>WISE, Alan ; JUPE, Steven C ; REES, Stephen</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c425t-7d675c189342abb42bc8b7229b213afac7331fd967a2b12969e403e9ec66a75b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Biological and medical sciences</topic><topic>Cell receptors</topic><topic>Cell structures and functions</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Humans</topic><topic>Ligands</topic><topic>Miscellaneous</topic><topic>Molecular and cellular biology</topic><topic>Receptors, G-Protein-Coupled - biosynthesis</topic><topic>Receptors, G-Protein-Coupled - physiology</topic><topic>Receptors, Nicotinic - metabolism</topic><topic>Sequence Homology, Amino Acid</topic><topic>Transfection</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>WISE, Alan</creatorcontrib><creatorcontrib>JUPE, Steven C</creatorcontrib><creatorcontrib>REES, Stephen</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Annual review of pharmacology and toxicology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>WISE, Alan</au><au>JUPE, Steven C</au><au>REES, Stephen</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The identification of ligands at orphan G-protein coupled receptors</atitle><jtitle>Annual review of pharmacology and toxicology</jtitle><addtitle>Annu Rev Pharmacol Toxicol</addtitle><date>2004-01-01</date><risdate>2004</risdate><volume>44</volume><issue>1</issue><spage>43</spage><epage>66</epage><pages>43-66</pages><issn>0362-1642</issn><eissn>1545-4304</eissn><abstract>The completion of the human genome sequencing project has identified approximately 720 genes that belong to the G-protein coupled receptor (GPCR) superfamily. Approximately half of these genes are thought to encode sensory receptors. Of the remaining 360 receptors, the natural ligand has been identified for approximately 210 receptors, leaving 150 so-called orphan GPCRs with no known ligand or function. The identification of ligands active at orphan GPCRs has been achieved through the development of a number of experimental approaches, including the screening of putative small molecule and peptide ligands, reverse pharmacology, and the use of bioinformatics to predict candidate ligands. In this review, we discuss the methodologies developed for the identification of ligands at orphan GPCRs and include examples of their successful application.</abstract><cop>Palo Alto, CA</cop><pub>Annual Reviews</pub><pmid>14744238</pmid><doi>10.1146/annurev.pharmtox.44.101802.121419</doi><tpages>24</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0362-1642
ispartof Annual review of pharmacology and toxicology, 2004-01, Vol.44 (1), p.43-66
issn 0362-1642
1545-4304
language eng
recordid cdi_proquest_miscellaneous_80123212
source Annual Reviews
subjects Biological and medical sciences
Cell receptors
Cell structures and functions
Fundamental and applied biological sciences. Psychology
Humans
Ligands
Miscellaneous
Molecular and cellular biology
Receptors, G-Protein-Coupled - biosynthesis
Receptors, G-Protein-Coupled - physiology
Receptors, Nicotinic - metabolism
Sequence Homology, Amino Acid
Transfection
title The identification of ligands at orphan G-protein coupled receptors
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-20T10%3A02%3A55IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=The%20identification%20of%20ligands%20at%20orphan%20G-protein%20coupled%20receptors&rft.jtitle=Annual%20review%20of%20pharmacology%20and%20toxicology&rft.au=WISE,%20Alan&rft.date=2004-01-01&rft.volume=44&rft.issue=1&rft.spage=43&rft.epage=66&rft.pages=43-66&rft.issn=0362-1642&rft.eissn=1545-4304&rft_id=info:doi/10.1146/annurev.pharmtox.44.101802.121419&rft_dat=%3Cproquest_cross%3E80123212%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c425t-7d675c189342abb42bc8b7229b213afac7331fd967a2b12969e403e9ec66a75b3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=80123212&rft_id=info:pmid/14744238&rfr_iscdi=true