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Phenomenology based multiscale models as tools to understand cell membrane and organelle morphologies

机译:基于现象学的多尺度模型作为了解细胞膜和细胞器形态的工具

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摘要

An intriguing question in cell biology is “how do cells regulate their shape?” It is commonly believed that the observed cellular morphologies are a result of the complex interaction among the lipid molecules (constituting the cell membrane), and with a number of other macromolecules, such as proteins. It is also believed that the common biophysical processes essential for the functioning of a cell also play an important role in cellular morphogenesis. At the cellular scale—where typical dimensions are in the order of micrometers—the effects arising from the molecular scale can either be modeled as equilibrium or non-equilibrium processes. In this chapter, we discuss the dynamically triangulated Monte Carlo technique to model and simulate membrane morphologies at the cellular scale, which in turn can be used to investigate several questions related to shape regulation in cells. In particular, we focus on two specific problems within the framework of isotropic and anisotropic elasticity theories: namely, (i) the origin of complex, physiologically relevant, membrane shapes due to the interaction of the membrane with curvature remodeling proteins, and (ii) the genesis of steady state cellular shapes due to the action of non-equilibrium forces that are generated by the fission and fusion of transport vesicles and by the binding and unbinding of proteins from the parent membrane.
机译:细胞生物学中一个有趣的问题是“细胞如何调节其形状?”通常认为,观察到的细胞形态是脂质分子(构成细胞膜)与许多其他大分子(例如蛋白质)之间复杂相互作用的结果。人们还认为,对于细胞功能至关重要的常见生物物理过程在细胞形态发生中也起着重要作用。在细胞尺度上(典型尺寸约为微米级),可以将分子尺度产生的效应建模为平衡或非平衡过程。在本章中,我们讨论了动态三角测量的蒙特卡洛技术,以在细胞尺度上建模和模拟膜的形态,进而可以用来研究与细胞形状调节有关的几个问题。特别是,我们关注各向同性和各向异性弹性理论框架内的两个具体问题:(i)由于膜与曲率重塑蛋白相互作用而产生的复杂的,生理相关的膜形状的起源,以及(ii)稳态细胞形状的发生是由于运输小泡的裂变和融合以及蛋白质与母膜的结合和解离所产生的非平衡力的作用。

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