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磷酸化在G蛋白偶联受体网格蛋白介导的内化调控中的作用

Role of Phosphorylation in the Control of Clathrin-Mediated Internalization of GPCR.

作者信息

Delom Frederic, Fessart Delphine

机构信息

Bordeaux Cardiothoracic Research Center, Bordeaux University, 146, Léo-Saignat, 33076 Bordeaux, France.

出版信息

Int J Cell Biol. 2011;2011:246954. doi: 10.1155/2011/246954. Epub 2011 Jun 7.

Abstract

The process by which G protein-coupled receptors (GPCRs) are internalized through the clathrin-coated vesicles involves interactions of multifunctional adaptor proteins. These interactions are tightly controlled by phosphorylation and dephosphorylation mechanisms resulting in the regulation of receptor endocytosis. However, the identities of the kinases involved in this process remained largely unknown until recently. This paper discusses advances in our knowledge of the important role played by protein phosphorylation in the regulation of the endocytic machinery and how phosphorylation controls the coated vesicle cycle.

摘要

G蛋白偶联受体(GPCRs)通过网格蛋白包被小泡进行内化的过程涉及多功能衔接蛋白的相互作用。这些相互作用受到磷酸化和去磷酸化机制的严格控制,从而导致受体胞吞作用的调节。然而,直到最近,参与这一过程的激酶的身份在很大程度上仍不为人知。本文讨论了我们在蛋白质磷酸化在调节内吞机制中所起的重要作用以及磷酸化如何控制包被小泡循环方面的知识进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/816a/3132527/b939649ab3e0/IJCB2011-246954.001.jpg

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