一种循环状态,可导致细胞内运输中的玻璃动力学

M. Scholz, S. Burov, Kimberly L. Weirich, B. Scholz, S. Tabei, M. Gardel, A. Dinner
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引用次数: 19

摘要

在活细胞中,已经观察到分子马达的幂律停留时间,但这些捕获状态的起源尚不清楚。我们介绍了在二维细丝网络上运动的电机的最小模型,其动力学模拟显示出与实验观察到的统计数据相当。对模型轨迹的分析,以及实验粒子跟踪数据,揭示了一种状态,在这种状态下,马达在三根或更多细丝的连接处无产出地循环。我们为这些结动力学制定了一个主方程,并表明从这种涡状状态中逃脱所需的时间可以解释幂律停留时间。为了进一步的实验验证,我们确定了运动价的动力学趋势。我们证明这些趋势存在于肌动蛋白网络上肌凝蛋白II的个体轨迹中。我们讨论细胞如何通过局部控制其细胞骨架网络结构来调节细胞内运输,进而调节生物功能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A cycling state that can lead to glassy dynamics in intracellular transport
Power-law dwell times have been observed for molecular motors in living cells, but the origins of these trapped states are not known. We introduce a minimal model of motors moving on a two-dimensional network of filaments, and simulations of its dynamics exhibit statistics comparable to those observed experimentally. Analysis of the model trajectories, as well as experimental particle tracking data, reveals a state in which motors cycle unproductively at junctions of three or more filaments. We formulate a master equation for these junction dynamics and show that the time required to escape from this vortex-like state can account for the power-law dwell times. We identify trends in the dynamics with the motor valency for further experimental validation. We demonstrate that these trends exist in individual trajectories of myosin II on an actin network. We discuss how cells could regulate intracellular transport and, in turn, biological function, by controlling their cytoskeletal network structures locally.
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