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:辛苷在提高肌动蛋白长丝的灵活性中的作用转向分子动力学分析

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摘要

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:甲毛蛋白是最重要的调节蛋白之一,并参与拆卸肌动蛋白长丝的过程。甲氯蛋白诱导肌动蛋白长丝的构象变化,以及该研究中长丝的弯曲和扭转刚性,我们研究了辛苷的作用对使用计算方法的肌动蛋白长丝的机械性能的影响。由其结合的钴素数定义的三种模型使用粗粒粒子的马蒂尼灭柱构成,然后用转向分子动力学模拟延伸。在获得模型的应力 - 应变曲线之后,我们计算尚未确定肌动蛋白丝的杨氏的模数和其他机械性能。我们根据原子的几何差异分析了三种模型的不同行为的原因。最后,证明Cofilin结合导致肌动蛋白长丝中残留物的距离,角度和稳定性的变化。 (c)2016年Elsevier B.v.保留所有权利。

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