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Force production by depolymerizing microtubules: load-velocity curves and run-pause statistics.

机译:通过微管解聚产生力:载荷-速度曲线和运行暂停统计。

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摘要

Experiments indicate that depolymerization of microtubules generates sufficient force to produce the minus-end-directed transport of chromosomes during mitosis (Koshland et al., 1988). In vitro, analogous transport of kinesin-coated microspheres exhibits a paradoxical effect. Minus-end-directed transport of the microspheres driven by depolymerization is enhanced by the presence of ATP, which fuels the motor action of kinesin driving the microspheres in the opposite direction, toward the plus end of the microtubule. Here we present a mathematical model to explain this behavior. We postulate that a microsphere at the plus end of the microtubule facilitates depolymerization and hence enhances minus-end-directed transport. The force-velocity curve of the model is derived; it has the peculiar feature that velocity is maximal at some positive load (opposing the motion) rather than at zero load. The model is used to simulate the stochastic process of microsphere-facilitated depolymerization-driven transport. Simulated trajectories at low load show distinctive runs and pauses, the statistics of which are calculated from the model. The statistics of the process provide sufficient information to determine all of the model's parameters.
机译:实验表明,在有丝分裂期间,微管的解聚产生足够的力以产生染色体的负端定向转运(Koshland等,1988)。在体外,驱动蛋白包被的微球的类似运输表现出自相矛盾的作用。由解聚作用驱动的微球的负端定向运输通过ATP的存在而得到增强,ATP促进了驱动蛋白的微球朝相反方向驱动微球正端的运动。在这里,我们提出一个数学模型来解释这种行为。我们假设在微管正端的微球有助于解聚,从而增强负端定向的运输。推导了模型的力-速度曲线。它具有独特的功能,即在某些正向负载(与运动相对)下,速度最大,而不是零负载。该模型用于模拟微球促进解聚驱动运输的随机过程。低负载下的模拟轨迹显示出独特的运行和暂停,其统计信息是根据模型计算得出的。过程的统计信息提供了足够的信息来确定模型的所有参数。

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