Molecular basis of receptor/G-protein-coupling selectivity

被引:347
作者
Wess, J [1 ]
机构
[1] NIDDKD, Bioorgan Chem Lab, NIH, Bethesda, MD 20892 USA
关键词
G-protein-coupled receptors; G-proteins; receptor activation; G-protein activation; receptor/G-protein interactions; receptor/G-protein coupling selectivity;
D O I
10.1016/S0163-7258(98)00030-8
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Molecular cloning studies have shown that G-protein coupled receptors form one of the largest protein families found in nature, and it is estimated that approximately 1000 different such receptors exist in mammals. Characteristically, when activated by the appropriate ligand, an individual receptor can recognize and activate only a limited set of the many structurally closely related heterotrimeric G-proteins expressed within a cell. To understand how this selectivity is achieved at a molecular level has become the focus of an ever increasing number of laboratories. This review provides an overview of recent structural, molecular genetic, biochemical, and biophysical studies that have led to novel insights into the molecular mechanisms governing receptor-mediated G-protein activation and receptor/G protein coupling selectivity. PHARMACOL. THER. 80(3):231-264, 1998. (C) 1998 Elsevier Science Inc.
引用
收藏
页码:231 / 264
页数:34
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