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测量和模拟微管产生的力。

Measuring and modeling forces generated by microtubules.

作者信息

Gudimchuk Nikita B, Alexandrova Veronika V

机构信息

Department of Physics, Lomonosov Moscow State University, Moscow, Russia.

Department of Biology, Lomonosov Moscow State University, Moscow, Russia.

出版信息

Biophys Rev. 2023 Oct 13;15(5):1095-1110. doi: 10.1007/s12551-023-01161-7. eCollection 2023 Oct.

DOI:10.1007/s12551-023-01161-7
PMID:37974983
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10643784/
Abstract

Tubulins are essential proteins, which are conserved across all eukaryotic species. They polymerize to form microtubules, cytoskeletal components of paramount importance for cellular mechanics. The microtubules combine an extraordinarily high flexural rigidity and a non-equilibrium behavior, manifested in their intermittent assembly and disassembly. These chemically fueled dynamics allow microtubules to generate significant pushing and pulling forces at their ends to reposition intracellular organelles, remodel membranes, bear compressive forces, and transport chromosomes during cell division. In this article, we review classical and recent studies, which have allowed the quantification of microtubule-generated forces. The measurements, to which we owe most of the quantitative information about microtubule forces, were carried out in biochemically reconstituted systems We also discuss how mathematical and computational modeling has contributed to the interpretations of these results and shaped our understanding of the mechanisms of force production by tubulin polymerization and depolymerization.

摘要

微管蛋白是所有真核生物物种中都保守的必需蛋白质。它们聚合形成微管,微管是细胞力学中至关重要的细胞骨架成分。微管兼具极高的抗弯刚度和非平衡行为,表现为其间歇性的组装和拆卸。这些由化学能驱动的动力学特性使微管能够在其末端产生显著的推拉力,以重新定位细胞内的细胞器、重塑膜结构、承受压力并在细胞分裂期间运输染色体。在本文中,我们回顾了经典研究和近期研究,这些研究使得对微管产生的力进行量化成为可能。我们所掌握的关于微管力的大部分定量信息都源自于在生化重构系统中所进行的测量。我们还将讨论数学和计算建模如何有助于对这些结果的解释,并塑造了我们对微管蛋白聚合和解聚产生力的机制的理解。

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Measuring and modeling forces generated by microtubules.测量和模拟微管产生的力。
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本文引用的文献

1
Compressive forces stabilize microtubules in living cells.压缩力使活细胞中的微管稳定。
Nat Mater. 2023 Jul;22(7):913-924. doi: 10.1038/s41563-023-01578-1. Epub 2023 Jun 29.
2
Unveiling the catalytic mechanism of GTP hydrolysis in microtubules.揭示微管中 GTP 水解的催化机制。
Proc Natl Acad Sci U S A. 2023 Jul 4;120(27):e2305899120. doi: 10.1073/pnas.2305899120. Epub 2023 Jun 26.
3
Stable kinetochore-microtubule attachment requires loop-dependent Ndc80-Ndc80 binding.稳定的动粒-微管连接需要环依赖的 Ndc80-Ndc80 结合。
EMBO J. 2023 Jul 3;42(13):e112504. doi: 10.15252/embj.2022112504. Epub 2023 May 19.
4
Working strokes produced by curling protofilaments at disassembling microtubule tips can be biochemically tuned and vary with species.在微管末端解聚时,原纤维卷曲产生的工作冲程可以在生化层面上进行调节,并且因物种而异。
Elife. 2022 Dec 29;11:e83225. doi: 10.7554/eLife.83225.
5
Beyond the GTP-cap: Elucidating the molecular mechanisms of microtubule catastrophe.超越 GTP 帽:阐明微管崩溃的分子机制。
Bioessays. 2023 Jan;45(1):e2200081. doi: 10.1002/bies.202200081. Epub 2022 Nov 18.
6
Theory of tip structure-dependent microtubule catastrophes and damage-induced microtubule rescues.尖端结构依赖性微管崩解理论和损伤诱导的微管拯救。
Proc Natl Acad Sci U S A. 2022 Nov 16;119(46):e2208294119. doi: 10.1073/pnas.2208294119. Epub 2022 Nov 7.
7
Strain stiffening of Ndc80 complexes attached to microtubule plus ends.Ndc80 复合物在微管正极端的应变硬化。
Biophys J. 2022 Nov 1;121(21):4048-4062. doi: 10.1016/j.bpj.2022.09.039. Epub 2022 Oct 4.
8
Estimation of microtubule-generated forces using a DNA origami nanospring.使用 DNA 折纸纳米弹簧估算微管产生的力。
J Cell Sci. 2023 Mar 1;136(5). doi: 10.1242/jcs.260154. Epub 2022 Oct 5.
9
Reconstitution of kinetochore motility and microtubule dynamics reveals a role for a kinesin-8 in establishing end-on attachments.重建动粒运动和微管动力学揭示了驱动蛋白-8 在建立端对端连接中的作用。
Elife. 2022 Jul 5;11:e78450. doi: 10.7554/eLife.78450.
10
Cross-linkers at growing microtubule ends generate forces that drive actin transport.生长中的微管末端的交联蛋白会产生力,从而驱动肌动蛋白运输。
Proc Natl Acad Sci U S A. 2022 Mar 15;119(11):e2112799119. doi: 10.1073/pnas.2112799119. Epub 2022 Mar 10.