Department of Biological Sciences and Bioengineering, Indian Institute of Technology, Kanpur 208016, India.
Department of Biological Sciences and Bioengineering, Indian Institute of Technology, Kanpur 208016, India.
Trends Cell Biol. 2017 Nov;27(11):851-862. doi: 10.1016/j.tcb.2017.05.008. Epub 2017 Jun 23.
G protein-coupled receptors (GPCRs) are major signal recognition and transmission units in the plasma membrane. The interaction of activated and phosphorylated GPCRs with the multifunctional adaptor proteins β-arrestins (βarrs) is crucial for regulation of their signaling and functional outcomes. Over the past few years, a range of structural, biochemical, and cellular studies have revealed novel insights into GPCR-βarr interaction and signaling. Some of these findings have come as a surprise and therefore have the potential to significantly refine the conceptual framework of the GPCR-βarr system. Here we discuss these recent advances with particular emphasis on biphasic GPCR-βarr interaction, the formation of GPCR-G-protein-βarr supercomplexes, and receptor-specific conformational signatures in βarrs. We also underline the emerging research areas that are likely to be at the center stage of investigations in the coming years.
G 蛋白偶联受体(GPCRs)是质膜中主要的信号识别和转导单元。激活和磷酸化的 GPCR 与多功能衔接蛋白β-arrestins(βarrs)的相互作用对于调节它们的信号转导和功能结果至关重要。在过去的几年中,一系列结构、生化和细胞研究揭示了 GPCR-βarr 相互作用和信号转导的新见解。其中一些发现令人惊讶,因此有可能显著完善 GPCR-βarr 系统的概念框架。在这里,我们特别强调双相 GPCR-βarr 相互作用、GPCR- G 蛋白-βarr 超复合物的形成以及βarrs 中受体特异性构象特征,讨论这些最新进展。我们还强调了可能成为未来几年研究中心的新兴研究领域。
Trends Cell Biol. 2017-6-23
Nat Commun. 2016-11-9
Curr Opin Struct Biol. 2022-8
Signal Transduct Target Ther. 2024-4-10
Front Pharmacol. 2023-5-30
Pharmacol Rev. 2023-9
Front Cell Dev Biol. 2023-3-10
Curr Opin Struct Biol. 2023-6
Antioxidants (Basel). 2022-8-18