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动粒处微管末端偶联的生物物理学

Biophysics of Microtubule End Coupling at the Kinetochore.

作者信息

Grishchuk Ekaterina L

机构信息

Department of Physiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, 19104, USA.

出版信息

Prog Mol Subcell Biol. 2017;56:397-428. doi: 10.1007/978-3-319-58592-5_17.

Abstract

The main physiological function of mitotic kinetochores is to provide durable attachment to spindle microtubules, which segregate chromosomes in order to partition them equally between the two daughter cells. Numerous kinetochore components that can bind directly to microtubules have been identified, including ATP-dependent motors and various microtubule-associated proteins with no motor activity. A major challenge facing the field is to explain chromosome motions based on the biochemical and structural properties of these individual kinetochore components and their assemblies. This chapter reviews the molecular mechanisms responsible for the motions associated with dynamic microtubule tips at the single-molecule level, as well as the activities of multimolecular ensembles called couplers. These couplers enable persistent kinetochore motion even under load, but their exact composition and structure remain unknown. Because no natural or artificial macro-machines function in an analogous manner to these molecular nano-devices, understanding their underlying biophysical mechanisms will require conceptual advances.

摘要

有丝分裂动粒的主要生理功能是与纺锤体微管形成持久连接,纺锤体微管分离染色体以便将其均等地分配到两个子细胞中。已鉴定出许多能直接与微管结合的动粒成分,包括ATP依赖型马达蛋白和各种无马达活性的微管相关蛋白。该领域面临的一个主要挑战是基于这些单个动粒成分及其组装体的生化和结构特性来解释染色体运动。本章回顾了在单分子水平上与动态微管末端相关运动的分子机制,以及被称为偶联器的多分子集合体的活性。这些偶联器即使在负载下也能使动粒持续运动,但其确切组成和结构仍不清楚。由于没有天然或人工的宏观机器以类似于这些分子纳米装置的方式发挥作用,理解其潜在的生物物理机制将需要概念上的进展。

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