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一种嵌合原核五聚体配体门控通道揭示了不同的激活途径。

A chimeric prokaryotic pentameric ligand-gated channel reveals distinct pathways of activation.

作者信息

Schmandt Nicolaus, Velisetty Phanindra, Chalamalasetti Sreevatsa V, Stein Richard A, Bonner Ross, Talley Lauren, Parker Mark D, Mchaourab Hassane S, Yee Vivien C, Lodowski David T, Chakrapani Sudha

机构信息

Department of Neuroscience, Department of Physiology and Biophysics, Department of Biochemistry, and Center for Proteomics and Bioinformatics, School of Medicine, Case Western Reserve University, Cleveland, OH 44106.

Department of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, TN 37232.

出版信息

J Gen Physiol. 2015 Oct;146(4):323-40. doi: 10.1085/jgp.201511478.

Abstract

Recent high resolution structures of several pentameric ligand-gated ion channels have provided unprecedented details of their molecular architecture. However, the conformational dynamics and structural rearrangements that underlie gating and allosteric modulation remain poorly understood. We used a combination of electrophysiology, double electron-electron resonance (DEER) spectroscopy, and x-ray crystallography to investigate activation mechanisms in a novel functional chimera with the extracellular domain (ECD) of amine-gated Erwinia chrysanthemi ligand-gated ion channel, which is activated by primary amines, and the transmembrane domain of Gloeobacter violaceus ligand-gated ion channel, which is activated by protons. We found that the chimera was independently gated by primary amines and by protons. The crystal structure of the chimera in its resting state, at pH 7.0 and in the absence of primary amines, revealed a closed-pore conformation and an ECD that is twisted with respect to the transmembrane region. Amine- and pH-induced conformational changes measured by DEER spectroscopy showed that the chimera exhibits a dual mode of gating that preserves the distinct conformational changes of the parent channels. Collectively, our findings shed light on both conserved and divergent features of gating mechanisms in this class of channels, and will facilitate the design of better allosteric modulators.

摘要

最近,几种五聚体配体门控离子通道的高分辨率结构为其分子结构提供了前所未有的细节。然而,门控和变构调节背后的构象动力学和结构重排仍知之甚少。我们结合电生理学、双电子-电子共振(DEER)光谱和X射线晶体学,研究了一种新型功能嵌合体的激活机制,该嵌合体具有被伯胺激活的菊欧文氏菌胺门控配体门控离子通道的细胞外结构域(ECD)和被质子激活的紫球藻配体门控离子通道的跨膜结构域。我们发现该嵌合体可被伯胺和质子独立门控。在pH 7.0且不存在伯胺的情况下,该嵌合体处于静息状态的晶体结构显示为闭孔构象,且ECD相对于跨膜区域发生扭曲。通过DEER光谱测量的胺和pH诱导的构象变化表明,该嵌合体表现出双重门控模式,保留了亲本通道独特的构象变化。总的来说,我们的研究结果揭示了这类通道门控机制的保守和不同特征,将有助于设计更好的变构调节剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3165/4586589/63a7db577eaa/JGP_201511478_Fig1.jpg

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