G蛋白偶联受体
逮捕
内体
生物
细胞生物学
变构调节
磷酸化
受体
信号转导
生物物理学
生物化学
细胞内
作者
John Janetzko,Ryoji Kise,Benjamin Barsi‐Rhyne,Dirk H Siepe,Franziska M. Heydenreich,Kouki Kawakami,Matthieu Masureel,Shoji Maeda,K. Christopher García,Mark von Zastrow,Asuka Inoue,Brian K. Kobilka
出处
期刊:Cell
[Elsevier]
日期:2022-11-01
卷期号:185 (24): 4560-4573.e19
被引量:43
标识
DOI:10.1016/j.cell.2022.10.018
摘要
Binding of arrestin to phosphorylated G protein-coupled receptors (GPCRs) is crucial for modulating signaling. Once internalized, some GPCRs remain complexed with β-arrestins, while others interact only transiently; this difference affects GPCR signaling and recycling. Cell-based and in vitro biophysical assays reveal the role of membrane phosphoinositides (PIPs) in β-arrestin recruitment and GPCR-β-arrestin complex dynamics. We find that GPCRs broadly stratify into two groups, one that requires PIP binding for β-arrestin recruitment and one that does not. Plasma membrane PIPs potentiate an active conformation of β-arrestin and stabilize GPCR-β-arrestin complexes by promoting a fully engaged state of the complex. As allosteric modulators of GPCR-β-arrestin complex dynamics, membrane PIPs allow for additional conformational diversity beyond that imposed by GPCR phosphorylation alone. For GPCRs that require membrane PIP binding for β-arrestin recruitment, this provides a mechanism for β-arrestin release upon translocation of the GPCR to endosomes, allowing for its rapid recycling.
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