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
[Cell Press]
日期:2022-11-01
卷期号:185 (24): 4560-4573.e19
被引量:121
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.
科研通智能强力驱动
Strongly Powered by AbleSci AI