Department of Biochemistry and Molecular Biology, Sidney Kimmel Medical College, Thomas Jefferson University, Philadelphia, PA 19107, USA.
Cells. 2021 Mar 4;10(3):555. doi: 10.3390/cells10030555.
Agonist activation of G protein-coupled receptors promotes sequential interaction of the receptor with heterotrimeric G proteins, G protein-coupled receptor kinases (GRKs), and arrestins. GRKs play a central role in mediating the switch from G protein to arrestin interaction and thereby control processes such as receptor desensitization and trafficking and arrestin-mediated signaling. In this review, I provide a historical perspective on some of the early studies that identified the family of GRKs with a primary focus on the non-visual GRKs. These studies included identification, purification, and cloning of the β-adrenergic receptor kinase in the mid- to late-1980s and subsequent cloning and characterization of additional members of the GRK family. This helped to lay the groundwork for ensuing work focused on understanding the structure and function of these important enzymes.
激动剂激活 G 蛋白偶联受体促进受体与异三聚体 G 蛋白、G 蛋白偶联受体激酶 (GRK) 和阻滞蛋白的顺序相互作用。GRK 在介导 G 蛋白与阻滞蛋白相互作用的转换中发挥核心作用,从而控制受体脱敏、转运以及阻滞蛋白介导的信号等过程。在这篇综述中,我提供了一些早期研究的历史视角,这些研究主要集中在非视觉 GRK 上。这些研究包括在 80 年代中后期鉴定β-肾上腺素能受体激酶家族,随后克隆并鉴定了 GRK 家族的其他成员。这为后续研究这些重要酶的结构和功能奠定了基础。