中间开放结构揭示了机械激活的PIEZO1通道的门控转变。

IF 14.7 1区 医学 Q1 NEUROSCIENCES
Neuron Pub Date : 2025-02-19 Epub Date: 2024-12-23 DOI:10.1016/j.neuron.2024.11.020
Sijia Liu, Xuzhong Yang, Xudong Chen, Xiaochun Zhang, Jinghui Jiang, Jingyi Yuan, Wenhao Liu, Li Wang, Heng Zhou, Kun Wu, Boxue Tian, Xueming Li, Bailong Xiao
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引用次数: 0

摘要

PIEZO1是一种机械激活的阳离子通道,经历力诱导的激活和失活。然而,其独特的结构状态仍未确定。在这里,我们使用了一个开放倾向的PIEZO1-S2472E突变体来捕获一个中间开放结构。与PIEZO1的弯曲和扁平结构相比,S2472E-Intermediate结构表现出部分扁平的叶片,上盖向下旋转运动,连接上盖与孔衬内螺旋的连接件类似弹簧的压缩。这些构象变化打开了帽门和疏水跨膜门,而细胞内侧塞门保持关闭。压电陶瓷具有上盖和闭合盖栅的扁平结构可能代表失活状态。离子传导的分子动力学(MD)模拟支持封闭、中间开放和失活的结构状态。诱变和电生理研究确定了PIEZO1机械激活的关键结构域和残基。这些研究共同定义了PIEZO1的不同结构状态和门控转变。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An intermediate open structure reveals the gating transition of the mechanically activated PIEZO1 channel.

PIEZO1 is a mechanically activated cation channel that undergoes force-induced activation and inactivation. However, its distinct structural states remain undefined. Here, we employed an open-prone PIEZO1-S2472E mutant to capture an intermediate open structure. Compared with the curved and flattened structures of PIEZO1, the S2472E-Intermediate structure displays partially flattened blades, a downward and rotational motion of the top cap, and a spring-like compression of the linker connecting the cap to the pore-lining inner helix. These conformational changes open the cap gate and the hydrophobic transmembrane gate, whereas the intracellular lateral plug gate remains closed. The flattened structure of PIEZO1 with an up-state cap and closed cap gate might represent an inactivated state. Molecular dynamics (MD) simulations of ion conduction support the closed, intermediate open, and inactivated structural states. Mutagenesis and electrophysiological studies identified key domains and residues critical for the mechanical activation of PIEZO1. These studies collectively define the distinct structural states and gating transitions of PIEZO1.

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来源期刊
Neuron
Neuron 医学-神经科学
CiteScore
24.50
自引率
3.10%
发文量
382
审稿时长
1 months
期刊介绍: Established as a highly influential journal in neuroscience, Neuron is widely relied upon in the field. The editors adopt interdisciplinary strategies, integrating biophysical, cellular, developmental, and molecular approaches alongside a systems approach to sensory, motor, and higher-order cognitive functions. Serving as a premier intellectual forum, Neuron holds a prominent position in the entire neuroscience community.
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