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
相关论文
共 112 条
[1]   AT1-receptor heterodimers show enhanced G-protein activation and altered receptor sequestration [J].
AbdAlla, S ;
Lother, H ;
Quitterer, U .
NATURE, 2000, 407 (6800) :94-98
[2]   14-3-3 and its possible role in co-ordinating multiple signalling pathways [J].
Aitken, A .
TRENDS IN CELL BIOLOGY, 1996, 6 (09) :341-347
[3]   Spinophilin, a novel protein phosphatase 1 binding protein localized to dendritic spines [J].
Allen, PB ;
Ouimet, CC ;
Greengard, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (18) :9956-9961
[4]   Detection of β2-adrenergic receptor dimerization in living cells using bioluminescence resonance energy transfer (BRET) [J].
Angers, S ;
Salahpour, A ;
Joly, E ;
Hilairet, S ;
Chelsky, D ;
Dennis, M ;
Bouvier, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (07) :3684-3689
[5]   Agonist-independent activation of metabotropic glutamate receptors by the intracellular protein Homer [J].
Ango, F ;
Prézeau, L ;
Muller, T ;
Tu, JC ;
Xiao, B ;
Worley, PF ;
Pin, JP ;
Bockaert, J ;
Fagni, L .
NATURE, 2001, 411 (6840) :962-965
[6]   THE CYCLOPHILIN HOMOLOG NINAA FUNCTIONS AS A CHAPERONE, FORMING A STABLE COMPLEX IN-VIVO WITH ITS PROTEIN TARGET RHODOPSIN [J].
BAKER, EK ;
COLLEY, NJ ;
ZUKER, CS .
EMBO JOURNAL, 1994, 13 (20) :4886-4895
[7]   Interaction of serotonin 5-hydroxytryptamine type 2C receptors with PDZ10 of the multi-PDZ domain protein MUPP1 [J].
Bécamel, C ;
Figge, A ;
Poliak, S ;
Dumuis, A ;
Peles, E ;
Bockaert, J ;
Lübbert, H ;
Ullmer, C .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (16) :12974-12982
[8]  
Benzing T, 2000, J BIOL CHEM, V275, P28167
[9]   Mammalian RGS proteins: Barbarians at the gate [J].
Berman, DM ;
Gilman, AG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (03) :1269-1272
[10]   Oligomerization of G-protein-coupled transmitter receptors [J].
Bouvier, M .
NATURE REVIEWS NEUROSCIENCE, 2001, 2 (04) :274-286