GPCR-interacting proteins (GIPs):: nature and functions

被引:78
作者
Bockaert, J [1 ]
Roussignol, G [1 ]
Bécamel, C [1 ]
Gavarini, S [1 ]
Joubert, L [1 ]
Dumuis, A [1 ]
Fagni, L [1 ]
Marin, P [1 ]
机构
[1] LGF, UPR CNRS 2580, F-34094 Montpellier 5, France
关键词
dendritic spine; G-protein-coupled receptor interacting protein; metabotropic; glutamate receptor; proteomics; serotonin receptor;
D O I
10.1042/BST0320851
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The simplistic idea that seven transmembrane receptors are single monomeric proteins that interact with heterotrimeric G-proteins after agonist binding is definitively out of date. Indeed, GPCRs (G-protein-coupled receptors) are part of multiprotein networks organized around scaffolding proteins. These GIN (GPCR-interacting proteins) are either transmembrane or cytosolic proteins. Proteomic approaches can be used to get global pictures of these 'receptosomes'. This approach allowed us to identify direct but also indirect binding partners of serotonin receptors. GIN are involved in a wide range of functions including control of the targeting, trafficking and signalling of GPCRs. One of them, Shank, which is a secondary and tertiary partner of metabotropic and ionotropic glutamate receptors, respectively, can induce the formation of a whole functional glutamate 'receptosome' and the structure to which it is associated, the dendritic spine.
引用
收藏
页码:851 / 855
页数:5
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