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从细胞角度看 G 蛋白偶联受体的偏倚。

A cellular perspective of bias at G protein-coupled receptors.

机构信息

Department of Chemical Physiology and Biochemistry, Oregon Health and Sciences University, Portland, Oregon, USA.

出版信息

Protein Sci. 2020 Jun;29(6):1345-1354. doi: 10.1002/pro.3872. Epub 2020 Apr 27.

Abstract

G protein-coupled receptors (GPCRs) modulate cell function over short- and long-term timescales. GPCR signaling depends on biochemical parameters that define the what, when, and where of receptor function: what proteins mediate and regulate receptor signaling, where within the cell these interactions occur, and how long these interactions persist. These parameters can vary significantly depending on the activating ligand. Collectivity, differential agonist activity at a GPCR is called bias or functional selectivity. Here we review agonist bias at GPCRs with a focus on ligands that show dramatically different cellular responses from their unbiased counterparts.

摘要

G 蛋白偶联受体 (GPCRs) 在短时间和长时间尺度上调节细胞功能。GPCR 信号取决于定义受体功能的“何时、何地、何物”的生化参数:介导和调节受体信号的蛋白、这些相互作用发生在细胞内的何处,以及这些相互作用持续多长时间。这些参数可能因激活配体而异。总的来说,GPCR 上的不同激动剂活性被称为偏倚或功能选择性。本文综述了 GPCR 激动剂偏倚,重点介绍了与其无偏激动剂相比显示出明显不同细胞反应的配体。

相似文献

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A cellular perspective of bias at G protein-coupled receptors.从细胞角度看 G 蛋白偶联受体的偏倚。
Protein Sci. 2020 Jun;29(6):1345-1354. doi: 10.1002/pro.3872. Epub 2020 Apr 27.
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Conformational Basis of G Protein-Coupled Receptor Signaling Versatility.G 蛋白偶联受体信号转导多功能性的构象基础。
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