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冷冻电镜在缝隙连接通道高分辨率结构分析中的潜力。

Potential of cryo-EM for high-resolution structural analysis of gap junction channels.

机构信息

Cellular and Structural Physiology Institute (CeSPI), Nagoya University, Furo-cho, Chikusa-ku, Nagoya 464-8601, Japan; Department of Basic Medicinal Sciences, Graduate School of Pharmaceutical Sciences, Nagoya University, Furo-cho, Chikusa-ku, Nagoya 464-8601, Japan.

出版信息

Curr Opin Struct Biol. 2019 Feb;54:78-85. doi: 10.1016/j.sbi.2019.01.005. Epub 2019 Feb 21.

Abstract

Gap junction family proteins form conduits connecting the cytoplasm of adjacent cells, thereby enabling electrical and chemical coupling to maintain physiological homeostasis. Gap junction proteins comprise two gene families, connexins in chordates and innexins in pre-chordates. Their channel structures have been analyzed by electron or X-ray crystallography, but only a few atomic structures have been reported. Recent advances in single-particle cryo-electron microscopy (cryo-EM) will help to elucidate these structures further. Here the structural biology of gap junction channels utilizing crystallography and single-particle cryo-EM is overviewed to shed light on the functional mechanisms of cell-cell communication that are essential for multicellular organisms.

摘要

缝隙连接家族蛋白形成连接相邻细胞质的管道,从而能够实现电和化学偶联,以维持生理内稳态。缝隙连接家族蛋白由两个基因家族组成:脊椎动物中的连接蛋白和原索动物中的连接小体蛋白。它们的通道结构已经通过电子或 X 射线晶体学进行了分析,但仅报道了少数原子结构。单颗粒冷冻电子显微镜(cryo-EM)的最新进展将有助于进一步阐明这些结构。本文综述了利用晶体学和单颗粒 cryo-EM 研究缝隙连接通道的结构生物学,以阐明细胞间通讯的功能机制,这对多细胞生物至关重要。

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