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Numerical Simulation of Nanoindentation and Patch Clamp Experiments on Mechanosensitive Channels of Large Conductance in Escherichia coli

机译:大肠杆菌中大电导率机械敏感通道的纳米压痕和膜片钳实验的数值模拟

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摘要

A hierarchical simulation framework that integrates information from all-atom simulations into a finite element model at the continuum level is established to study the mechanical response of a mechanosensitive channel of large conductance (MscL) in bacteria Escherichia coli (E. coli) embedded in a vesicle formed by the dipalmitoylphosphatidycholine (DPPC) lipid bilayer. Sufficient structural details of the protein are built into the continuum model, with key parameters and material properties derived from molecular mechanics simulations. The multi-scale framework is used to analyze the gating of MscL when the lipid vesicle is subjective to nanoindentation and patch clamp experiments, and the detailed structural transitions of the protein are obtained explicitly as a function of external load; it is currently impossible to derive such information based solely on all-atom simulations. The gating pathways of E. coli-MscL qualitatively agree with results from previous patch clamp experiments. The gating mechanisms under complex indentation-induced deformation are also predicted. This versatile hierarchical multi-scale framework may be further extended to study the mechanical behaviors of cells and biomolecules, as well as to guide and stimulate biomechanics experiments.
机译:建立了一个层次化的模拟框架,该框架将来自所有原子模拟的信息集成到连续水平的有限元模型中,以研究嵌入在细菌中的大肠杆菌(E. coli)中大电导(MscL)的机械敏感通道的机械响应。由二棕榈酰磷脂酰胆碱(DPPC)脂质双层形成的囊泡。蛋白质的足够结构细节已内置到连续模型中,其关键参数和材料特性均来自分子力学模拟。当脂质囊泡经受纳米压痕和膜片钳实验时,使用多尺度框架分析MscL的门控,并明确获得蛋白质的详细结构转变,这是外部负载的函数。目前不可能仅基于全原子模拟来得出此类信息。大肠杆菌-MscL的门控途径在质量上与以前的膜片钳实验结果一致。还预测了在复杂压痕引起的变形下的浇口机理。这种通用的分层多尺度框架可以进一步扩展以研究细胞和生物分子的机械行为,并指导和刺激生物力学实验。

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