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驱动蛋白运动的理论形式体系I. 由单个单头驱动蛋白驱动的珠子运动。

Theoretical formalism for kinesin motility I. Bead movement powered by single one-headed kinesins.

作者信息

Chen Y d

机构信息

Mathematical Research Branch, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland 20892-2690 USA.

出版信息

Biophys J. 2000 Jan;78(1):313-21. doi: 10.1016/S0006-3495(00)76594-5.

DOI:10.1016/S0006-3495(00)76594-5
PMID:10620295
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1300639/
Abstract

The directional movement on a microtubule of a plastic bead connected elastically to a single one-headed kinesin motor is studied theoretically. The kinesin motor can bind and unbind to periodic binding sites on the microtubule and undergo conformational changes while catalyzing the hydrolysis of ATP. An analytic formalism relating the dynamics of the bead and the ATP hydrolysis cycle of the motor is derived so that the calculation of the average velocity of the bead can be easily carried out. The formalism was applied to a simple three-state biochemical model to investigate how the velocity of the bead movement is affected by the external load, the diffusion coefficient of the bead, and the stiffness of the elastic element connecting the bead and the motor. The bead velocity was found to be critically dependent on the diffusion coefficient of the bead and the stiffness of the elastic element. A linear force-velocity relation was found for the model no matter whether the bead velocity was modulated by the diffusion coefficient of the bead or by the externally applied load. The formalism should be useful in modeling the mechanisms of chemimechanical coupling in kinesin motors based on in vitro motility data.

摘要

从理论上研究了与单个单头驱动蛋白马达弹性连接的塑料珠在微管上的定向运动。驱动蛋白马达能够与微管上的周期性结合位点结合和解离,并在催化ATP水解时发生构象变化。推导了一种将珠子动力学与马达ATP水解循环相关联的解析形式,以便能够轻松计算珠子的平均速度。该形式被应用于一个简单的三态生化模型,以研究珠子运动速度如何受到外部负载、珠子的扩散系数以及连接珠子与马达的弹性元件的刚度的影响。发现珠子速度严重依赖于珠子的扩散系数和弹性元件的刚度。无论珠子速度是由珠子的扩散系数还是由外部施加的负载调节,该模型都呈现出线性的力 - 速度关系。这种形式对于基于体外运动数据建立驱动蛋白马达中的化学机械偶联机制模型应该是有用的。

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本文引用的文献

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Chemically Driven Motility of Brownian Particles.
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Direction determination in the minus-end-directed kinesin motor ncd.负端定向驱动蛋白ncd中的方向确定
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Microtubule-dependent vesicle transport: modulation of channel and transporter activity in liver and kidney.微管依赖性囊泡运输:肝脏和肾脏中通道及转运体活性的调节
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One-headed kinesin derivatives move by a nonprocessive, low-duty ratio mechanism unlike that of two-headed kinesin.与双头驱动蛋白不同,单头驱动蛋白衍生物通过一种非持续性、低负载率机制移动。
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Kinetic mechanism of monomeric non-claret disjunctional protein (Ncd) ATPase.单体非红葡萄酒分离蛋白(Ncd)ATP酶的动力学机制
J Biol Chem. 1997 Dec 5;272(49):30735-40. doi: 10.1074/jbc.272.49.30735.
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Coupling of kinesin steps to ATP hydrolysis.驱动蛋白步移与ATP水解的偶联。
Nature. 1997 Jul 24;388(6640):390-3. doi: 10.1038/41118.