Department of Biotechnology, University of Verona, Ca' Vignal 1: strada le Grazie 15, I-37134 Verona, Italy.
Curr Protein Pept Sci. 2013 Dec;14(8):650-7. doi: 10.2174/13892037113146660085.
Phospholipases C beta (PLC-βs) are essential components of the signal transduction of metazoans. They catalyze the production of the second messengers inositol-1,4,5-trisphosphate (IP3) and diacylglycerol (DAG) from the hydrolysis of phosphatidylinositol-4,5-bisphosphate (PIP2). These enzymes are activated by G-protein-coupled receptors (GPCRs) through the interaction with the alpha subunit of heterotrimeric G-proteins belonging to the Gq family (Gαq), the Gβγ subunits released by the inhibitory G-protein (Gi) and Ca2+ ions. Here we review current structural insights on these important proteins, with a particular focus on the most structurally characterized isoform (PLC-β3) and the activation mechanism operated by Gαq. We propose, following the lead of recent studies, that a tight combination of experiments and molecular simulations are instrumental in further enlightening the structure/function understanding of PLC-βs.
磷酯酶 Cβ(PLC-βs)是后生动物信号转导的必需组成部分。它们通过磷脂酰肌醇-4,5-二磷酸(PIP2)的水解,催化第二信使肌醇-1,4,5-三磷酸(IP3)和二酰基甘油(DAG)的生成。这些酶通过与异三聚体 G 蛋白(Gαq)的α亚基的相互作用而被 G 蛋白偶联受体(GPCRs)激活,Gαq 是 G 蛋白偶联受体(GPCRs)释放的 Gβγ 亚基和抑制性 G 蛋白(Gi)释放的 Ca2+离子。在这里,我们回顾了这些重要蛋白质的当前结构见解,特别关注结构特征最明显的同工型(PLC-β3)和 Gαq 所操作的激活机制。我们建议,根据最近的研究,实验和分子模拟的紧密结合对于进一步阐明 PLC-βs 的结构/功能理解是非常重要的。