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The patterned assembly and stepwise Vps4-mediated disassembly of composite ESCRT-III polymers drives archaeal cell division
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...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10017037/ https://www.ncbi.nlm.nih.gov/pubmed/36921039 http://dx.doi.org/10.1126/sciadv.ade5224 |
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author | Hurtig, Fredrik Burgers, Thomas C. Q. Cezanne, Alice Jiang, Xiuyun Mol, Frank N. Traparić, Jovan Pulschen, Andre Arashiro Nierhaus, Tim Tarrason-Risa, Gabriel Harker-Kirschneck, Lena Löwe, Jan Šarić, Anđela Vlijm, Rifka Baum, Buzz |
author_facet | Hurtig, Fredrik Burgers, Thomas C. Q. Cezanne, Alice Jiang, Xiuyun Mol, Frank N. Traparić, Jovan Pulschen, Andre Arashiro Nierhaus, Tim Tarrason-Risa, Gabriel Harker-Kirschneck, Lena Löwe, Jan Šarić, Anđela Vlijm, Rifka Baum, Buzz |
author_sort | Hurtig, Fredrik |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-10017037 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-100170372023-03-16 The patterned assembly and stepwise Vps4-mediated disassembly of composite ESCRT-III polymers drives archaeal cell division Hurtig, Fredrik Burgers, Thomas C. Q. Cezanne, Alice Jiang, Xiuyun Mol, Frank N. Traparić, Jovan Pulschen, Andre Arashiro Nierhaus, Tim Tarrason-Risa, Gabriel Harker-Kirschneck, Lena Löwe, Jan Šarić, Anđela Vlijm, Rifka Baum, Buzz Sci Adv Biomedicine and Life Sciences 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. American Association for the Advancement of Science 2023-03-15 /pmc/articles/PMC10017037/ /pubmed/36921039 http://dx.doi.org/10.1126/sciadv.ade5224 Text en Copyright © 2023 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution License 4.0 (CC BY). https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution license (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Biomedicine and Life Sciences Hurtig, Fredrik Burgers, Thomas C. Q. Cezanne, Alice Jiang, Xiuyun Mol, Frank N. Traparić, Jovan Pulschen, Andre Arashiro Nierhaus, Tim Tarrason-Risa, Gabriel Harker-Kirschneck, Lena Löwe, Jan Šarić, Anđela Vlijm, Rifka Baum, Buzz The patterned assembly and stepwise Vps4-mediated disassembly of composite ESCRT-III polymers drives archaeal cell division |
title | The patterned assembly and stepwise Vps4-mediated disassembly of composite ESCRT-III polymers drives archaeal cell division |
title_full | The patterned assembly and stepwise Vps4-mediated disassembly of composite ESCRT-III polymers drives archaeal cell division |
title_fullStr | The patterned assembly and stepwise Vps4-mediated disassembly of composite ESCRT-III polymers drives archaeal cell division |
title_full_unstemmed | The patterned assembly and stepwise Vps4-mediated disassembly of composite ESCRT-III polymers drives archaeal cell division |
title_short | The patterned assembly and stepwise Vps4-mediated disassembly of composite ESCRT-III polymers drives archaeal cell division |
title_sort | patterned assembly and stepwise vps4-mediated disassembly of composite escrt-iii polymers drives archaeal cell division |
topic | Biomedicine and Life Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10017037/ https://www.ncbi.nlm.nih.gov/pubmed/36921039 http://dx.doi.org/10.1126/sciadv.ade5224 |
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