G蛋白偶联受体
G蛋白偶联受体激酶
逮捕
细胞生物学
信号转导
视紫红质样受体
生物
磷酸化
受体
β肾上腺素能受体激酶
G蛋白
生物化学
兴奋剂
代谢受体
作者
Vsevolod V. Gurevich,Eugenia V. Gurevich
标识
DOI:10.3389/fphar.2019.00125
摘要
Every animal species expresses hundreds of different G protein-coupled receptors (GPCRs) that respond to a wide variety of external stimuli. GPCRs-driven signaling pathways are involved in pretty much every physiological function and in many pathologies. Therefore, GPCRs are targeted by about a third of clinically used drugs. The signaling of most GPCRs via G proteins is terminated by the phosphorylation of active receptor by specific kinases (GPCR kinases, or GRKs) and subsequent binding of arrestin proteins, that selectively recognize active phosphorylated receptors. In addition, GRKs and arrestins play a role in multiple signaling pathways in the cell, both GPCR-initiated and receptor-independent. Here we focus on the mechanisms of GRK- and arrestin-mediated regulation of GPCR signaling, which includes homologous desensitization and redirection of signaling to additional pathways by bound arrestins.
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