驱动蛋白-13 MCAK 微管解聚酶的模型研究。

IF 2.2 4区 生物学 Q3 BIOPHYSICS
Ping Xie
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引用次数: 0

摘要

有丝分裂中心粒相关驱动蛋白(MCAK)马达蛋白是驱动蛋白-13 家族的典型成员,可以从正负两端解聚微管。MCAK马达的一个关键问题是它如何进行解聚酶活动。为了解决这个问题,本文介绍了MCAK马达在微管上移动并解聚微管的途径。在此基础上,理论研究了野生型和突变型MCAK马达的动力学,包括全长MCAK、马达结构域α4-螺旋发生突变的全长MCAK、颈部中和的突变全长MCAK、单体MCAK和颈部中和的突变单体MCAK。研究表明,单个二聚体 MCAK 马达能以进程方式解聚微管,每次可移除一个微管蛋白或两个微管蛋白。理论结果与现有的实验数据一致。此外,还提供了预测结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Modeling study of kinesin-13 MCAK microtubule depolymerase

Modeling study of kinesin-13 MCAK microtubule depolymerase

Modeling study of kinesin-13 MCAK microtubule depolymerase

Mitotic centromere-associated kinesin (MCAK) motor protein is a typical member of the kinesin-13 family, which can depolymerize microtubules from both plus and minus ends. A critical issue for the MCAK motor is how it performs the depolymerase activity. To address the issue, the pathway of the MCAK motor moving on microtubules and depolymerizing the microtubules is presented here. On the basis of the pathway, the dynamics of both the wild-type and mutant MCAK motors is studied theoretically, which include the full-length MCAK, the full-length MCAK with mutations in the α4-helix of the motor domain, the mutant full-length MCAK with a neutralized neck, the monomeric MCAK and the mutant monomeric MCAK with a neutralized neck. The studies show that a single dimeric MCAK motor can depolymerize microtubules in a processive manner, with either one tubulin or two tubulins being removed per times. The theoretical results are in agreement with the available experimental data. Moreover, predicted results are provided.

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来源期刊
European Biophysics Journal
European Biophysics Journal 生物-生物物理
CiteScore
4.30
自引率
0.00%
发文量
43
审稿时长
6-12 weeks
期刊介绍: The journal publishes papers in the field of biophysics, which is defined as the study of biological phenomena by using physical methods and concepts. Original papers, reviews and Biophysics letters are published. The primary goal of this journal is to advance the understanding of biological structure and function by application of the principles of physical science, and by presenting the work in a biophysical context. Papers employing a distinctively biophysical approach at all levels of biological organisation will be considered, as will both experimental and theoretical studies. The criteria for acceptance are scientific content, originality and relevance to biological systems of current interest and importance. Principal areas of interest include: - Structure and dynamics of biological macromolecules - Membrane biophysics and ion channels - Cell biophysics and organisation - Macromolecular assemblies - Biophysical methods and instrumentation - Advanced microscopics - System dynamics.
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