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Gating Mechanisms of Mechanosensitive Channels of Large Conductance II: Systematic Study of Conformational Transitions

机译:大电导的机械敏感通道的门控机制II:构象转变的系统研究

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摘要

Part II of this study is based on the continuum mechanics-based molecular dynamics-decorated finite element method (MDeFEM) framework established in Part I. In Part II, the gating pathways of Escherichia coli-MscL channels under various basic deformation modes are simulated. Upon equibiaxial tension (which is verified to be the most effective mode for gating), the MDeFEM results agree well with both experiments and all-atom simulations in literature, as well as the analytical continuum models and elastic network models developed in Part I. Different levels of model sophistication and effects of structural motifs are explored in detail, where the importance of mechanical roles of transmembrane helices, cytoplasmic helices, and loops are discussed. The conformation transitions under complex membrane deformations are predicted, including bending, torsion, cooperativity, patch clamp, and indentation. Compared to atom-based molecular dynamics simulations and elastic network models, the MDeFEM framework is unusually well-suited for simulating complex deformations at large length scales. The versatile hierarchical framework can be further applied to simulate the gating transition of other mechanosensitive channels and other biological processes where mechanical perturbation is important.
机译:本研究的第二部分基于在第一部分中建立的基于连续力学的分子动力学修饰有限元方法(MDeFEM)框架。在第二部分中,模拟了各种基本变形模式下大肠杆菌MscL通道的门控路径。在等双轴拉力下(经证实是最有效的门控方式),MDeFEM结果与文献中的实验和全原子模拟以及在第一部分中开发的分析连续体模型和弹性网络模型都非常吻合。详细探讨了模型的复杂程度和结构基序的影响,并讨论了跨膜螺旋,胞质螺旋和环的机械作用的重要性。可以预测复杂膜变形下的构象转变,包括弯曲,扭转,协同作用,膜片钳和压痕。与基于原子的分子动力学模拟和弹性网络模型相比,MDeFEM框架非常适合于模拟大尺寸的复杂变形。通用的分层框架可以进一步应用于模拟其他机械敏感通道和其他生物过程的门控转换,其中机械干扰很重要。

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