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谷氨酸受体离子通道组装、激活和调节的结构和机制。

Structure and mechanism of glutamate receptor ion channel assembly, activation and modulation.

机构信息

Laboratory of Cellular and Molecular Neurophysiology, Porter Neuroscience Research Center, NICHD, NIH, DHHS, Bethesda, MD 20892, United States.

出版信息

Curr Opin Neurobiol. 2011 Apr;21(2):283-90. doi: 10.1016/j.conb.2011.02.001. Epub 2011 Feb 23.

Abstract

Ionotropic glutamate receptors (iGluRs) are ligand gated ion channels that mediate excitatory synaptic transmission in the brain of vertebrates. A rapidly growing body of crystal structures for isolated iGluR extracellular domains, and more recently a full length AMPA receptor, combined with data from electrophysiological experiments and MD simulations, provides a framework that makes it possible to investigate the molecular basis for assembly, gating and modulation. These unprecedented advances in structural biology are constantly challenged by novel functional properties that emerge despite decades of functional analysis, and by a growing family of auxiliary proteins that modulate iGluR activity and assembly.

摘要

离子型谷氨酸受体 (iGluRs) 是配体门控离子通道,在脊椎动物的大脑中介导兴奋性突触传递。越来越多的分离的 iGluR 细胞外结构域的晶体结构,以及最近的全长 AMPA 受体的晶体结构,结合来自电生理实验和 MD 模拟的数据,为研究组装、门控和调节的分子基础提供了一个框架。尽管经过几十年的功能分析,这些结构生物学的空前进展仍然不断受到新的功能特性的挑战,而且辅助蛋白家族的不断增加也调节 iGluR 的活性和组装。

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