The patterned assembly and stepwise Vps4-mediated disassembly of composite ESCRT-III polymers drives archaeal cell division

Author:

Hurtig Fredrik1ORCID,Burgers Thomas C. Q.2ORCID,Cezanne Alice1ORCID,Jiang Xiuyun3ORCID,Mol Frank N.2ORCID,Traparić Jovan1ORCID,Pulschen Andre Arashiro1,Nierhaus Tim1ORCID,Tarrason-Risa Gabriel1ORCID,Harker-Kirschneck Lena4ORCID,Löwe Jan1ORCID,Šarić Anđela5ORCID,Vlijm Rifka2ORCID,Baum Buzz1ORCID

Affiliation:

1. Medical Research Council Laboratory of Molecular Biology, Cambridge CB2 0QH, UK.

2. Molecular Biophysics, Zernike Institute for Advanced Materials, University of Groningen, 9747 AG Groningen, Netherlands.

3. Laboratory of Soft Matter Physics, The Institute of Physics, Chinese Academy of Sciences, Beijing, China.

4. University College London, Institute for the Physics of Living Systems, WC1E 6BT London, UK.

5. Institute of Science and Technology Austria, 3400 Klosterneuburg, Austria.

Abstract

ESCRT-III family proteins form composite polymers that deform and cut membrane tubes in the context of a wide range of cell biological processes across the tree of life. In reconstituted systems, sequential changes in the composition of ESCRT-III polymers induced by the AAA–adenosine triphosphatase Vps4 have been shown to remodel membranes. However, it is not known how composite ESCRT-III polymers are organized and remodeled in space and time in a cellular context. Taking advantage of the relative simplicity of the ESCRT-III–dependent division system in Sulfolobus acidocaldarius , one of the closest experimentally tractable prokaryotic relatives of eukaryotes, we use super-resolution microscopy, electron microscopy, and computational modeling to show how CdvB/CdvB1/CdvB2 proteins form a precisely patterned composite ESCRT-III division ring, which undergoes stepwise Vps4-dependent disassembly and contracts to cut cells into two. These observations lead us to suggest sequential changes in a patterned composite polymer as a general mechanism of ESCRT-III–dependent membrane remodeling.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

Cited by 8 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3