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G蛋白偶联受体的膜运输

Membrane trafficking of G protein-coupled receptors.

作者信息

Tan Christopher M, Brady Ashley E, Nickols Hilary Highfield, Wang Qin, Limbird Lee E

机构信息

Department of Pharmacology, Vanderbilt University Medical Center, Nashville, Tennessee 37232, USA.

出版信息

Annu Rev Pharmacol Toxicol. 2004;44:559-609. doi: 10.1146/annurev.pharmtox.44.101802.121558.

Abstract

G protein-coupled receptors (GPCRs) modulate diverse physiological and behavioral signaling pathways by virtue of changes in receptor activation and inactivation states. Functional changes in receptor properties include dynamic interactions with regulatory molecules and trafficking to various cellular compartments at various stages of the life cycle of a GPCR. This review focuses on trafficking of GPCRs to the cell surface, stabilization there, and agonist-regulated turnover. GPCR interactions with a variety of newly revealed partners also are reviewed with the intention of provoking further analysis of the relevance of these interactions in GPCR trafficking, signaling, or both. The disease consequences of mislocalization of GPCRs also are described.

摘要

G蛋白偶联受体(GPCRs)通过受体激活和失活状态的变化来调节多种生理和行为信号通路。受体特性的功能变化包括与调节分子的动态相互作用以及在GPCR生命周期的各个阶段转运至不同的细胞区室。本综述聚焦于GPCRs向细胞表面的转运、在细胞表面的稳定以及激动剂调节的周转。还综述了GPCR与各种新发现的伴侣分子的相互作用,旨在引发对这些相互作用在GPCR转运、信号传导或两者中的相关性的进一步分析。还描述了GPCR定位错误的疾病后果。

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