Catterall William A, Zheng Ning
Department of Pharmacology, Box 357280, University of Washington, Seattle, WA 98195, USA.
Department of Pharmacology, Box 357280, University of Washington, Seattle, WA 98195, USA; Howard Hughes Medical Institute, Box 357280, University of Washington, Seattle, WA 98195, USA.
Trends Biochem Sci. 2015 Sep;40(9):526-34. doi: 10.1016/j.tibs.2015.07.002. Epub 2015 Aug 5.
Voltage-gated sodium channels (NaVs) and calcium channels (CaVs) are involved in electrical signaling, contraction, secretion, synaptic transmission, and other physiological processes activated in response to depolarization. Despite their physiological importance, the structures of these closely related proteins have remained elusive because of their size and complexity. Bacterial NaVs have structures analogous to a single domain of eukaryotic NaVs and CaVs and are their likely evolutionary ancestor. Here we review recent work that has led to new understanding of NaVs and CaVs through high-resolution structural studies of their prokaryotic ancestors. New insights into their voltage-dependent activation and inactivation, ion conductance, and ion selectivity provide realistic structural models for the function of these complex membrane proteins at the atomic level.
电压门控钠通道(NaV)和钙通道(CaV)参与电信号传导、收缩、分泌、突触传递以及其他响应去极化而激活的生理过程。尽管它们在生理上具有重要意义,但由于其大小和复杂性,这些密切相关蛋白质的结构一直难以捉摸。细菌NaV的结构类似于真核生物NaV和CaV的单个结构域,并且可能是它们的进化祖先。在此,我们回顾了最近的研究工作,这些工作通过对其原核祖先进行高分辨率结构研究,使我们对NaV和CaV有了新的认识。对它们的电压依赖性激活和失活、离子传导以及离子选择性的新见解,为这些复杂膜蛋白在原子水平上的功能提供了逼真的结构模型。