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模拟微管在解聚驱动运输中的作用:一种蒙特卡洛方法。

Simulating the role of microtubules in depolymerization-driven transport: a Monte Carlo approach.

作者信息

Tao Y C, Peskin C S

机构信息

Department of Physics, New York University, New York 10003, USA.

出版信息

Biophys J. 1998 Sep;75(3):1529-40. doi: 10.1016/S0006-3495(98)74072-X.

DOI:10.1016/S0006-3495(98)74072-X
PMID:9726955
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1299828/
Abstract

In this paper we present a model that simulates the role of microtubules in depolymerization-driven transport. The model simulates a system that consists of a 13-protofilament microtubule with "five-start" helical structure and a motor protein-coated bead that moves along one of the protofilaments of the microtubule, as in in vitro experiments. The microtubule is simulated using the lateral cap model, with substantial generalizations. For the new terminal configurations in the presence of the bead, rate constants for association and dissociation events of tubulin molecules are calculated by exploring the geometric similarities between different patterns of terminal configurations and by decomposing complex patterns into simpler patterns whose corresponding rate constants are known. In comparison with a previous model, in which simplifications are made about the structure of the microtubule and in which the microtubule can only depolymerize, the detailed structure of the microtubule is taken into account in the present model. Furthermore, the microtubule can be either polymerizing or depolymerizing. Force-velocity curves are obtained for both zero and non-zero tubulin guanosine 5'-triphosphate (GTP) concentrations. By analyzing the trajectory of the bead under different parameters, the condition for "run and pause" is analyzed, and the time scale of "run" and "pause" is found to be different for different motor proteins. We also suggest experiments that can be used to examine the results predicted by the model.

摘要

在本文中,我们提出了一个模拟微管在解聚驱动运输中作用的模型。该模型模拟了一个系统,该系统由具有“五起始”螺旋结构的13原纤维微管和一个沿微管的其中一条原纤维移动的、涂有运动蛋白的珠子组成,如同体外实验那样。微管是使用侧向帽模型进行模拟的,并做了大量推广。对于存在珠子时的新末端构型,通过探索不同末端构型模式之间的几何相似性,并将复杂模式分解为已知相应速率常数的更简单模式,来计算微管蛋白分子结合和解离事件的速率常数。与之前的模型相比,之前的模型对微管结构进行了简化,且微管只能解聚,而本模型考虑了微管的详细结构。此外,微管既可以聚合也可以解聚。在微管蛋白鸟苷5'-三磷酸(GTP)浓度为零和非零的情况下都获得了力-速度曲线。通过分析不同参数下珠子的轨迹,分析了“运行和暂停”的条件,并且发现不同运动蛋白的“运行”和“暂停”时间尺度不同。我们还提出了可用于检验该模型预测结果的实验。

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引用本文的文献

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In vitro assays to study the tracking of shortening microtubule ends and to measure associated forces.用于研究缩短的微管末端追踪及测量相关力的体外测定。
Methods Cell Biol. 2010;95:657-76. doi: 10.1016/S0091-679X(10)95033-4.
2
Different assemblies of the DAM1 complex follow shortening microtubules by distinct mechanisms.DAM1复合体的不同组装体通过不同机制追踪缩短的微管。
Proc Natl Acad Sci U S A. 2008 May 13;105(19):6918-23. doi: 10.1073/pnas.0801811105. Epub 2008 May 6.
3
In search of an optimal ring to couple microtubule depolymerization to processive chromosome motions.寻找一种最佳环,以将微管解聚与进行性染色体运动相耦合。
Proc Natl Acad Sci U S A. 2007 Nov 27;104(48):19017-22. doi: 10.1073/pnas.0709524104. Epub 2007 Nov 20.
4
Force production by depolymerizing microtubules: a theoretical study.微管解聚产生的力:一项理论研究。
Proc Natl Acad Sci U S A. 2005 Mar 22;102(12):4353-8. doi: 10.1073/pnas.0501142102. Epub 2005 Mar 14.

本文引用的文献

1
Physical aspects of the growth and regulation of microtubule structures.微管结构生长与调控的物理方面。
Phys Rev Lett. 1993 Mar 1;70(9):1347-1350. doi: 10.1103/PhysRevLett.70.1347.
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The load dependence of kinesin's mechanical cycle.驱动蛋白机械循环的负载依赖性。
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Dynamic instability of microtubules: Monte Carlo simulation and application to different types of microtubule lattice.微管的动态不稳定性:蒙特卡罗模拟及其在不同类型微管晶格中的应用
Biophys J. 1993 Aug;65(2):578-96. doi: 10.1016/S0006-3495(93)81091-9.
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A new role for motor proteins as couplers to depolymerizing microtubules.运动蛋白作为与解聚微管耦合器的新角色。
J Cell Biol. 1995 Jan;128(1-2):1-4. doi: 10.1083/jcb.128.1.1.
10
Minus-end-directed motion of kinesin-coated microspheres driven by microtubule depolymerization.由微管解聚驱动的驱动蛋白包被微球的负端定向运动。
Nature. 1995 Jan 12;373(6510):161-4. doi: 10.1038/373161a0.