G protein-coupled receptor interacting proteins: Emerging roles in localization and signal transduction

被引:196
作者
Brady, AE [1 ]
Limbird, LE [1 ]
机构
[1] Vanderbilt Univ, Med Ctr, Nashville, TN 37232 USA
关键词
GPCR; scaffolding protein; chaperone; GPCR dirner; G protein signalling; protein-protein interaction;
D O I
10.1016/S0898-6568(01)00239-X
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The mechanism by which G protein-coupled receptors (GPCRs) translate extracellular signals into cellular changes initially was envisioned as a simple linear model: activation of the receptor by agonist binding leads to dissociation of the heterotrimeric GTP-binding G protein into its alpha and betagamma subunits, both of which can activate or inhibit various downstream effector molecules. The plethora of recently described multidomain scaffolding proteins and accessory/chaperone molecules that interact with GPCR, including GPCR themselves as homo- or heterodimers, provides for diverse molecular mechanisms for ligand recognition, signalling specificity, and receptor trafficking, This review will summarize the recently described GPCR-interacting proteins and their individual functional roles, as understood, Implicit in the search for the functional relevance of these interactions is the expectation that enhancement or disruption of target cell-specific events could serve as highly selective therapeutic opportunities. (C) 2002 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:297 / 309
页数:13
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