Roberts Jonathan A, Vial Catherine, Digby Helen R, Agboh Kelvin C, Wen Hairuo, Atterbury-Thomas Amelia, Evans Richard J
Department of Cell Physiology & Pharmacology, Medical Sciences Building, University of Leicester, Leicester, LE1 9HN, UK.
Pflugers Arch. 2006 Aug;452(5):486-500. doi: 10.1007/s00424-006-0073-6. Epub 2006 Apr 11.
P2X receptors for adenosine tri-phosphate (ATP) are a distinct family of ligand-gated cation channels with two transmembrane domains, intracellular amino and carboxy termini and a large extracellular ligand binding loop. Seven genes (P2X(1-7)) have been cloned and the channels form as either homo or heterotrimeric channels giving rise to a wide range of phenotypes. This review aims to give an account of recent work on the molecular basis of the properties of P2X receptors. In particular, to consider emerging information on the assembly of P2X receptor subunits, channel regulation and desensitisation, targeting, the molecular basis of drug action and the functional contribution of P2X receptors to physiological processes.
三磷酸腺苷(ATP)的P2X受体是一类独特的配体门控阳离子通道家族,具有两个跨膜结构域、细胞内氨基和羧基末端以及一个大的细胞外配体结合环。已克隆出七个基因(P2X(1 - 7)),这些通道可形成同三聚体或异三聚体通道,产生多种表型。本综述旨在阐述P2X受体特性分子基础的近期研究工作。特别是要探讨有关P2X受体亚基组装、通道调节与脱敏、靶向作用、药物作用分子基础以及P2X受体对生理过程功能贡献的新信息。