James S R, Downes C P
Department of Biochemistry, Medical Sciences Institute, University of Dundee, Scotland, UK.
Cell Signal. 1997 Aug;9(5):329-36. doi: 10.1016/s0898-6568(96)00175-1.
The production of the intracellular second messengers inositol (1,4,5)-trisphosphate (InsP3) and sn 1,2-diacylglycerol (DG) in response to a wide variety of extracellular primary messengers is achieved by an extended family of inositol phospholipid phosphodiesterases termed phospholipases C (PLC, E.C. 3.1.4.11). This family has been the subject of extensive research and it is clear that the different isoenzymes exhibit some common characteristics (e.g., interactions with substrates) and other distinctive features (e.g., modes of regulation). The recent description of the X-ray crystal structure of a mammalian PLC has served to clarify much about the behaviour of the PLCs, emphasising the "modular" structure of these enzymes. The main focus of this review will concern the specific adaptations of PLC molecules which make them efficient lipid-metabolising enzymes. We also describe what is known about how these enzymes interact with their lipid substrates, which will serve as a basis for considering how PLCs may be activated.
细胞内第二信使肌醇(1,4,5)-三磷酸(InsP3)和sn-1,2-二酰甘油(DG)对多种细胞外初级信使作出反应,这是由一个称为磷脂酶C(PLC,E.C. 3.1.4.11)的肌醇磷脂磷酸二酯酶大家族实现的。这个家族一直是广泛研究的对象,很明显,不同的同工酶表现出一些共同特征(例如,与底物的相互作用)和其他独特特征(例如,调节方式)。最近对一种哺乳动物PLC的X射线晶体结构的描述有助于阐明许多关于PLC行为的问题,强调了这些酶的“模块化”结构。本综述的主要重点将是PLC分子的特定适应性,这些适应性使它们成为高效的脂质代谢酶。我们还描述了关于这些酶如何与其脂质底物相互作用的已知信息,这将作为考虑PLC如何被激活的基础。