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质子化通过多个结构域的协调运动来控制 ASIC1a 的活性。

Protonation controls ASIC1a activity via coordinated movements in multiple domains.

机构信息

Department of Pharmacology and Toxicology, University of Lausanne, 1005 Lausanne, Switzerland.

出版信息

J Gen Physiol. 2014 Jan;143(1):105-18. doi: 10.1085/jgp.201311053. Epub 2013 Dec 16.

Abstract

Acid-sensing ion channels (ASICs) are neuronal Na(+)-conducting channels activated by extracellular acidification. ASICs are involved in pain sensation, expression of fear, and neurodegeneration after ischemic stroke. Functional ASICs are composed of three identical or homologous subunits, whose extracellular part has a handlike structure. Currently, it is unclear how protonation of residues in extracellular domains controls ASIC activity. Knowledge of these mechanisms would allow a rational development of drugs acting on ASICs. Protonation may induce conformational changes that control the position of the channel gate. We used voltage-clamp fluorometry with fluorophores attached to residues in different domains of ASIC1a to detect conformational changes. Comparison of the timing of fluorescence and current signals identified residues involved in movements that preceded desensitization and may therefore be associated with channel opening or early steps leading to desensitization. Other residues participated in movements intimately linked to desensitization and recovery from desensitization. Fluorescence signals of all mutants were detected at more alkaline pH than ionic currents. Their midpoint of pH dependence was close to that of steady-state desensitization, whereas the steepness of the pH fluorescence relationship was closer to that of current activation. A sequence of movements was observed upon acidification, and its backward movements during recovery from desensitization occurred in the reverse order, indicating that the individual steps are interdependent. Furthermore, the fluorescence signal of some labeled residues in the finger domain was strongly quenched by a Trp residue in the neighboring β-ball domain. Upon channel activation, their fluorescence intensity increased, indicating that the finger moved away from the β ball. This extensive analysis of activity-dependent conformational changes in ASICs sheds new light on the mechanisms by which protonation controls ASIC activity.

摘要

酸敏离子通道 (ASICs) 是一种神经元钠离子通道,可被细胞外酸化激活。ASICs 参与疼痛感知、恐惧表达以及缺血性中风后的神经退行性变。功能性 ASICs 由三个相同或同源的亚基组成,其细胞外部分具有手状结构。目前,尚不清楚细胞外结构域中残基的质子化如何控制 ASIC 活性。了解这些机制将允许合理开发作用于 ASIC 的药物。质子化可能诱导控制通道门位置的构象变化。我们使用带有附着于 ASIC1a 不同结构域残基的荧光团的电压钳荧光法来检测构象变化。荧光和电流信号的时间比较确定了参与脱敏前运动的残基,因此可能与通道开放或导致脱敏的早期步骤相关。其他残基参与与脱敏和脱敏恢复密切相关的运动。所有突变体的荧光信号都在比离子电流更碱性的 pH 值下被检测到。它们的 pH 值依赖关系的中点接近于稳态脱敏的中点,而 pH 值荧光关系的陡峭度更接近于电流激活的陡峭度。在酸化时观察到一系列运动,并且在脱敏恢复期间其反向运动以相反的顺序发生,表明各个步骤是相互依存的。此外,β 球域中相邻的色氨酸残基强烈猝灭指域中一些标记残基的荧光信号。通道激活时,它们的荧光强度增加,表明指状结构从 β 球上移开。对 ASICs 中活性依赖性构象变化的广泛分析为质子化控制 ASIC 活性的机制提供了新的认识。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65f4/3874563/9eaa7f5e0f60/JGP_201311053_Fig1.jpg

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