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首页> 外文期刊>Biophysical Chemistry: An International Journal Devoted to the Physical Chemistry of Biological Phenomena >Steered molecular dynamics analysis of the role of cofilin in increasing the flexibility of actin filaments
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Steered molecular dynamics analysis of the role of cofilin in increasing the flexibility of actin filaments

机译:可控蛋白在增加肌动蛋白丝柔韧性中作用的分子动力学动力学分析

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Cofilin is one of the most essential regulatory proteins and participates in the process of disassembling actin filaments. Cofilin induces conformational changes to actin filaments, and both the bending and torsional rigidity of the filament In this study, we investigate the effects of cofilin on the mechanical properties of actin filaments using computational methods. Three models defined by their number of bound cofilin are constructed using coarse-grained MARTINI force field, and they are then extended with steered molecular dynamics simulation. After obtaining the stress-strain curves of the models, we calculate their Young's moduli and other mechanical properties that have not yet been determined for actin filaments. We analyze the cause of the different behaviors of the three models based on their atomistic geometrical differences. Finally, it is demonstrated that cofilin binding causes changes in the distances, angles, and stabilities of the residues in actin filaments. (C) 2016 Elsevier B.V. All rights reserved.
机译:Cofilin是最重要的调节蛋白之一,并参与肌动蛋白丝的拆卸过程。 Cofilin诱导肌动蛋白丝的构象变化,以及丝的弯曲和扭转刚度在这项研究中,我们使用计算方法研究了Cofilin对肌动蛋白丝力学性能的影响。使用粗糙粒状的MARTINI力场构建了三个模型,这些模型由其结合的cofilin的数量定义,然后通过操纵分子动力学模拟进行扩展。获得模型的应力-应变曲线后,我们计算尚未确定的肌动蛋白丝的杨氏模量和其他机械性能。基于它们的原子几何差异,我们分析了这三种模型行为不同的原因。最后,证明了肌动蛋白丝的结合导致肌动蛋白丝中残基的距离,角度和稳定性的改变。 (C)2016 Elsevier B.V.保留所有权利。

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