Pitcher J A, Freedman N J, Lefkowitz R J
Howard Hughes Medical Institute, Department of Medicine (Cardiology), Duke University Medical Center, Durham, North Carolina 27710, USA.
Annu Rev Biochem. 1998;67:653-92. doi: 10.1146/annurev.biochem.67.1.653.
G protein-coupled receptor kinases (GRKs) constitute a family of six mammalian serine/threonine protein kinases that phosphorylate agonist-bound, or activated, G protein-coupled receptors (GPCRs) as their primary substrates. GRK-mediated receptor phosphorylation rapidly initiates profound impairment of receptor signaling, or desensitization. This review focuses on the regulation of GRK activity by a variety of allosteric and other factors: agonist-stimulated GPCRs, beta gamma subunits of heterotrimeric GTP-binding proteins, phospholipid cofactors, the calcium-binding proteins calmodulin and recoverin, posttranslational isoprenylation and palmitoylation, autophosphorylation, and protein kinase C-mediated GRK phosphorylation. Studies employing recombinant, purified proteins, cell culture, and transgenic animal models attest to the general importance of GRKs in regulating a vast array of GPCRs both in vitro and in vivo.
G蛋白偶联受体激酶(GRKs)构成了一个由六种哺乳动物丝氨酸/苏氨酸蛋白激酶组成的家族,这些激酶将激动剂结合的或活化的G蛋白偶联受体(GPCRs)磷酸化作为其主要底物。GRK介导的受体磷酸化迅速引发受体信号传导的严重损伤或脱敏。本综述重点关注多种变构和其他因素对GRK活性的调节:激动剂刺激的GPCRs、异源三聚体GTP结合蛋白的βγ亚基、磷脂辅因子、钙结合蛋白钙调蛋白和恢复蛋白、翻译后异戊二烯化和棕榈酰化、自磷酸化以及蛋白激酶C介导的GRK磷酸化。使用重组、纯化蛋白、细胞培养和转基因动物模型的研究证明了GRKs在体外和体内调节大量GPCRs方面的普遍重要性。