Orphan G-protein-coupled receptors and natural ligand discovery

被引:230
作者
Howard, AD
McAllister, G
Feighner, SD
Liu, QY
Nargund, RP
Van der Ploeg, LHT
Patchett, AA
机构
[1] Merck Res Labs, Dept Metab Disorders, Rahway, NJ 07065 USA
[2] Merck Sharp & Dohme Ltd, Neurosci Res Ctr, Res Labs, Dept Biochem, Harlow CM20 2QR, Essex, England
[3] Merck Res Labs, Dept Pharmacol, W Point, PA 19486 USA
[4] Merck Res Labs, Dept Med Chem, Rahway, NJ 07065 USA
关键词
D O I
10.1016/S0165-6147(00)01636-9
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The superfamily of seven-transmembrane-domain G-protein-coupled receptors (GPCRs) is the largest and most diverse group of transmembrane proteins involved in signal transduction, Each of the similar to 1000 family members found in vertebrates responds to stimuli as diverse as hormones, neurotransmitters, odorants and light, which selectively activate intracellular signaling events mediated by heterotrimeric G proteins. Because GPCRs are centrally positioned in the plasma membrane to initiate a cascade of cellular responses by diverse extracellular mediators, it is not surprising that modulation of GPCR function has been successful in the development of many marketed therapeutic agents. It has become clear that GPCRs far which a natural activating ligand has not yet been identified (orphan GPCRs) might provide a path to discovering new cellular substances that are important in human physiology The process of'de-orphanizing' these novel proteins has accelerated significantly and opened up new avenues for research in human physiology and pharmacology.
引用
收藏
页码:132 / 140
页数:9
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