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Molecular modeling of membrane curvature driven by epsin

机译:epsin驱动的膜曲率分子模型

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摘要

A molecular description of membrane curvature induction by the ENTH domain of the protein epsin has the potential to shed light on clathrin mediated endocytosis and its effect on pathological cell signaling processes. To that end, we are performing coarse-grained and all-atom molecular dynamics simulations of membrane remodeling by epsin. Coarse-grained simulations are used to characterize the local stress distribution throughout the membrane, yielding a microscopic picture of the induced curvature field, the additive effects of multiple epsins, and the role of surface tension in mediating epsin-membrane interactions.
机译:由蛋白epsin的ENTH域诱导的膜曲率的分子描述具有揭示网格蛋白介导的内吞作用及其对病理细胞信号转导过程的影响的潜力。为此,我们正在通过epsin进行膜重塑的粗粒度和全原子分子动力学模拟。粗粒度模拟用于表征整个膜的局部应力分布,从而产生诱导曲率场的微观图像,多种epsin的累加效应以及表面张力在介导epsin-膜相互作用中的作用。

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