Suppr超能文献

动力蛋白利用微管的主动涨落实现更快移动。

Dynein Harnesses Active Fluctuations of Microtubules for Faster Movement.

作者信息

Ezber Yasin, Belyy Vladislav, Can Sinan, Yildiz Ahmet

机构信息

Physics Department, University of California, Berkeley CA 94720 USA.

Biophysics Graduate Group, University of California, Berkeley CA 94720 USA.

出版信息

Nat Phys. 2020;16:312-316. doi: 10.1038/s41567-019-0757-4. Epub 2020 Jan 20.

Abstract

The cytoskeleton forms a dynamic network that generates fluctuations larger than thermal agitation of the cytoplasm. Here, we tested whether dynein, a minus-end-directed microtubule (MT) motor, can harness energy from these fluctuations using optical trapping . We show that dynein forms an asymmetric slip bond with MTs, where its detachment rate increases more slowly under hindering forces than assisting forces. This asymmetry enables dynein to generate unidirectional motility towards the minus-end from force fluctuations. Consistent with our model, oscillatory forces exerted by the trap drive dynein stepping without net force and ATP. Dynein is capable of ratcheting towards the minus-end even when the net force is in the plus-end direction. With ATP, force oscillations increase the velocity and stall force of dynein as it transports cargos and glides MTs. Therefore, dynein is a mechanical ratchet that rectifies cytoskeletal fluctuations to move faster and resists higher forces along MTs.

摘要

细胞骨架形成一个动态网络,产生比细胞质热搅动更大的波动。在此,我们测试了动力蛋白(一种向负端移动的微管马达蛋白)是否能利用光镊从这些波动中获取能量。我们发现动力蛋白与微管形成不对称的滑动键,在阻碍力作用下其脱离速率比助力作用下增加得更慢。这种不对称性使动力蛋白能够从力的波动中产生向负端的单向运动。与我们的模型一致,光镊施加的振荡力驱动动力蛋白步进而无需净力和ATP。即使净力指向正端方向,动力蛋白也能够朝着负端棘轮运动。有ATP时,力的振荡会增加动力蛋白运输货物和使微管滑动时的速度和失速力。因此,动力蛋白是一种机械棘轮,它矫正细胞骨架波动以更快移动并沿微管抵抗更大的力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8e8/8049612/7254943a1ce7/nihms-1543378-f0005.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验