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G蛋白偶联受体的非磷酸化依赖性脱敏作用?

Phosphorylation-independent desensitization of G protein-coupled receptors?

作者信息

Pao Christina S, Benovic Jeffrey L

机构信息

The Kimmel Cancer Center, Department of Microbiology and Immunology, Thomas Jefferson University, 233 South 10th Street, Philadelphia, PA 19107, USA.

出版信息

Sci STKE. 2002 Oct 8;2002(153):pe42. doi: 10.1126/stke.2002.153.pe42.

Abstract

G protein-coupled receptors (GPCRs) are involved in a multitude of signaling processes and respond to a wide range of ligands. The activity of GPCRs is subject to three principal modes of regulation: desensitization, trafficking, and down-regulation. Desensitization is defined as a loss in the responsiveness of a signaling system. The generally established paradigm for GPCR desensitization involves receptor phosphorylation by GPCR kinases (GRKs), initiated by agonist-induced conformational changes in the receptor or by kinases activated by specific signaling pathways. GRKs have several interaction domains and may be able to contribute to receptor desensitization through mechanisms that do not involve the kinase activity of GRK. Pao and Benovic discuss some of these interactions and their relevance for the regulation of GPCR signaling.

摘要

G蛋白偶联受体(GPCRs)参与多种信号传导过程,并对多种配体作出反应。GPCRs的活性受到三种主要调节模式的影响:脱敏、转运和下调。脱敏被定义为信号系统反应性的丧失。GPCR脱敏的普遍确立的范式涉及GPCR激酶(GRKs)介导的受体磷酸化,这是由激动剂诱导的受体构象变化或由特定信号通路激活的激酶引发的。GRKs具有多个相互作用结构域,并且可能能够通过不涉及GRK激酶活性的机制促进受体脱敏。Pao和Benovic讨论了其中一些相互作用及其与GPCR信号调节的相关性。

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