Institute of Medical Physics and Biophysics (CC2), Charité - Universitätsmedizin Berlin, Charitéplatz 1, 10117 Berlin, Germany; Group Protein X-ray Crystallography & Signal Transduction, Germany.
Institute of Medical Physics and Biophysics (CC2), Charité - Universitätsmedizin Berlin, Charitéplatz 1, 10117 Berlin, Germany.
Curr Opin Struct Biol. 2017 Aug;45:160-169. doi: 10.1016/j.sbi.2017.05.001. Epub 2017 Jun 7.
The large and multifunctional family of G protein-coupled receptors (GPCRs) are regulated by a small family of structurally conserved arrestin proteins. In order to bind an active GPCR, arrestin must first be activated by interaction with the phosphorylated receptor C-terminus. Recent years have witnessed major developments in high-resolution crystal structures of pre-active arrestins and arrestin or arrestin-derived peptides in complex with an active GPCR. Although each structure individually offers only a limited snapshot, taken together and interpreted in light of recent complementary functional data, they offer valuable insight into how arrestin is activated by and couples to a phosphorylated active GPCR.
G 蛋白偶联受体(GPCRs)是一个庞大而多功能的家族,由一小家族结构保守的 arrestin 蛋白调节。为了结合活性 GPCR,arrestin 必须首先通过与磷酸化受体 C 端相互作用而被激活。近年来,在预激活 arrestin 和与活性 GPCR 结合的 arrestin 或 arrestin 衍生肽的高分辨率晶体结构方面取得了重大进展。尽管每个结构单独提供的只是一个有限的快照,但结合起来并根据最近的互补功能数据进行解释,它们为了解 arrestin 如何被磷酸化的活性 GPCR 激活和偶联提供了有价值的见解。