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慢速和快速分子马达系统中的协同行为机制。

Mechanism of cooperative behaviour in systems of slow and fast molecular motors.

作者信息

Larson Adam G, Landahl Eric C, Rice Sarah E

机构信息

Department of Cell and Molecular Biology, Northwestern University, Chicago, IL 60611, USA.

出版信息

Phys Chem Chem Phys. 2009 Jun 28;11(24):4890-8. doi: 10.1039/b900968j. Epub 2009 May 11.

DOI:10.1039/b900968j
PMID:19506764
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2745065/
Abstract

Two recent theoretical advances have described cargo transport by multiple identical motors and by multiple oppositely directed, but otherwise identical motors [M. J. Muller, S. Klumpp and R. Lipowsky, Proc. Natl. Acad. Sci. U. S. A., 2008, 105(12), 4609-4614; S. Klumpp and R. Lipowsky, Proc. Natl. Acad. Sci. U. S. A., 2005, 102(48), 17284-17289]. Here, we combine a similar theoretical approach with a simple experiment to describe the behaviour of a system comprised of slow and fast molecular motors having the same directionality. We observed the movement of microtubules by mixtures of slow and fast kinesin motors attached to a glass coverslip in a classic sliding filament assay. The motors are identical, except that the slow ones contain five point mutations that collectively reduce their velocity approximately 15-fold without compromising maximal ATPase activity. Our results indicate that a small fraction of fast motors are able to accelerate the dissociation of slow motors from microtubules. Because of this, a sharp, highly cooperative transition occurs from slow to fast microtubule movement as the relative number of fast motors in the assay is increased. Microtubules move at half-maximal velocity when only 15% of the motors in the assay are fast. Our model indicates that this behaviour depends primarily on the relative motor velocities and the asymmetry between their forward and backward dissociation forces. It weakly depends on the number of motors and their processivity. We predict that movement of cargoes bound to two types of motors having very different velocities will be dominated by one or the other motor. Therefore, cargoes can potentially undergo abrupt changes in movement in response to regulatory mechanisms acting on only a small fraction of motors.

摘要

最近的两项理论进展描述了由多个相同的马达以及多个方向相反但其他方面相同的马达进行的货物运输[M. J. 米勒、S. 克伦普和R. 利波夫斯基,《美国国家科学院院刊》,2008年,105(12),4609 - 4614;S. 克伦普和R. 利波夫斯基,《美国国家科学院院刊》,2005年,102(48),17284 - 17289]。在此,我们将一种类似的理论方法与一个简单实验相结合,以描述由具有相同方向性的慢速和快速分子马达组成的系统的行为。我们在经典的滑动丝实验中,观察了附着在玻璃盖玻片上的慢速和快速驱动蛋白马达混合物对微管的运动。这些马达是相同的,只是慢速马达含有五个点突变,这些突变共同使它们的速度降低了约15倍,而不影响最大ATP酶活性。我们的结果表明,一小部分快速马达能够加速慢速马达从微管上的解离。因此,随着实验中快速马达相对数量的增加,微管运动从慢速到快速会发生急剧的、高度协同的转变。当实验中只有15%的马达是快速马达时,微管以半最大速度移动。我们的模型表明,这种行为主要取决于马达的相对速度以及它们向前和向后解离力之间的不对称性。它对马达数量及其持续性的依赖性较弱。我们预测,与两种速度差异很大的马达结合的货物的运动将由其中一种或另一种马达主导。因此,货物可能会因仅作用于一小部分马达的调节机制而在运动中发生突然变化。

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Heterogeneity in kinesin function.驱动蛋白功能的异质性。
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本文引用的文献

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Negative interference dominates collective transport of kinesin motors in the absence of load.在无负载情况下,负干扰主导驱动蛋白分子马达的集体运输。
Phys Chem Chem Phys. 2009 Jun 28;11(24):4882-9. doi: 10.1039/b900964g. Epub 2009 Apr 20.
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Transport by populations of fast and slow kinesins uncovers novel family-dependent motor characteristics important for in vivo function.快速和慢速驱动蛋白群体的运输揭示了对体内功能很重要的新的家族依赖性运动特征。
Biophys J. 2014 Oct 21;107(8):1896-1904. doi: 10.1016/j.bpj.2014.09.009.
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Multimotor transport in a system of active and inactive kinesin-1 motors.在由活性和非活性驱动蛋白-1 马达组成的系统中的多马达运输。
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Motor mutants bring wild-type motors to a halt stochastically.运动突变体随机使野生型运动停止。
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Backsteps induced by nucleotide analogs suggest the front head of kinesin is gated by strain.核苷酸类似物诱导的向后步移表明驱动蛋白的前端头部受应变门控。
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