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机械应力会降低肌动蛋白丝扭转和弯曲波动的幅度。

Mechanical Stress Decreases the Amplitude of Twisting and Bending Fluctuations of Actin Filaments.

机构信息

Department of Applied Bioscience, Kanazawa Institute of Technology, Ishikawa, Japan.

Department of Biological Science, Graduate School of Sciences, Nagoya University, 464-8601 Nagoya, Japan.

出版信息

J Mol Biol. 2023 Nov 15;435(22):168295. doi: 10.1016/j.jmb.2023.168295. Epub 2023 Oct 11.

Abstract

A variety of biological roles of mechanical forces have been proposed in cell biology, such as cell signaling pathways for survival, development, growth, and differentiation. Mechanical forces alter the mechanical conditions within cells and their environment, which strongly influences the reorganization of the actin cytoskeleton. Single-molecule imaging studies of actin filaments have led to the hypothesis that the actin filament acts as a mechanosensor; e.g., increases in actin filament tension alter their conformation and affinity for regulatory proteins. However, our understanding of the molecular mechanisms underlying how tension modulates the mechanical behavior of a single actin filament is still incomplete. In this study, a direct measurement of the twisting and bending of a fluorescently labeled single actin filament under different tension levels by force application (0.8-3.4 pN) was performed using single-molecule fluorescence polarization (SMFP) microscopy. The results showed that the amplitude of twisting and bending fluctuations of a single actin filament decreased with increasing tension. Electron micrograph analysis of tensed filaments also revealed that the fluctuations in the crossover length of actin filaments decreased with increasing filament tension. Possible molecular mechanisms underlying these results involving the binding of actin-binding proteins, such as cofilin, to the filament are discussed.

摘要

力学在细胞生物学中具有多种生物学作用,例如细胞存活、发育、生长和分化的信号通路。力学改变细胞及其环境内的力学条件,这强烈影响肌动蛋白细胞骨架的重组。肌动蛋白丝的单分子成像研究提出了肌动蛋白丝作为机械感受器的假说;例如,肌动蛋白丝张力的增加会改变其构象和与调节蛋白的亲和力。然而,我们对于张力如何调节单个肌动蛋白丝的力学行为的分子机制的理解仍不完整。在这项研究中,通过力施加(0.8-3.4 pN),使用单分子荧光偏振(SMFP)显微镜直接测量了在不同张力水平下荧光标记的单个肌动蛋白丝的扭曲和弯曲。结果表明,随着张力的增加,单个肌动蛋白丝的扭曲和弯曲波动幅度减小。拉紧丝的电子显微镜分析还表明,肌动蛋白丝交叉长度的波动随着丝张力的增加而减小。讨论了这些结果涉及的可能的分子机制,包括肌动蛋白结合蛋白(如胞质分裂蛋白)与丝的结合。

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