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动力蛋白-14 HSET 和 KlpA 是具有负载依赖性动力冲程的非进行性微管马达。

Kinesin-14 HSET and KlpA are non-processive microtubule motors with load-dependent power strokes.

机构信息

Department of Biochemistry and Gruss Lipper Biophotonics Center, Albert Einstein College of Medicine, Bronx, NY, USA.

Cell Biology, Neurobiology and Biophysics, Department of Biology, Faculty of Science, Utrecht University, CH, Utrecht, The Netherlands.

出版信息

Nat Commun. 2024 Aug 3;15(1):6564. doi: 10.1038/s41467-024-50990-x.

Abstract

Accurate chromosome segregation during cell division relies on coordinated actions of microtubule (MT)-based motor proteins in the mitotic spindle. Kinesin-14 motors play vital roles in spindle assembly and maintenance by crosslinking antiparallel MTs at the spindle midzone and anchoring spindle MTs' minus ends at the poles. In this study, we investigate the force generation and motility of the Kinesin-14 motors HSET and KlpA. Our findings reveal that both motors are non-processive, producing single load-dependent power strokes per MT encounter, with estimated load-free power strokes of ~30 and ~35 nm, respectively. Each homodimeric motor generates forces of ~0.5 pN, but when assembled in teams, they cooperate to generate forces of 1 pN or more. Notably, the cooperative activity among multiple motors leads to increased MT-sliding velocities. These results quantitatively elucidate the structure-function relationship of Kinesin-14 motors and underscore the significance of cooperative behavior in their cellular functions.

摘要

在细胞分裂过程中,染色体的精确分离依赖于有丝分裂纺锤体中微管(MT)-基础动力蛋白的协调作用。驱动蛋白-14 (Kinesin-14) 马达在纺锤体组装和维持中发挥着重要作用,通过在纺锤体中间区交联成对的 MT,并将纺锤体 MT 的负端锚定在两极。在这项研究中,我们研究了 Kinesin-14 马达 HSET 和 KlpA 的力产生和运动性。我们的研究结果表明,这两种马达都是非进展性的,在与每条 MT 的每次接触中产生单负载依赖性动力冲程,估计无负载动力冲程分别约为 30 和 35nm。每个同源二聚体马达产生约 0.5pN 的力,但当组装成团队时,它们会合作产生 1pN 或更大的力。值得注意的是,多个马达之间的合作活动导致 MT 滑动速度增加。这些结果定量阐明了 Kinesin-14 马达的结构-功能关系,并强调了其在细胞功能中合作行为的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc6f/11297315/0c162697add5/41467_2024_50990_Fig1_HTML.jpg

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