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The cryo-EM structure of the bacterial flagellum cap complex suggests a molecular mechanism for filament elongation
The bacterial flagellum is a remarkable molecular motor, whose primary function in bacteria is to facilitate motility through the rotation of a filament protruding from the bacterial cell. A cap complex, consisting of an oligomer of the protein FliD, is localized at the tip of the flagellum, and is...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7316729/ https://www.ncbi.nlm.nih.gov/pubmed/32587243 http://dx.doi.org/10.1038/s41467-020-16981-4 |
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author | Al-Otaibi, Natalie S. Taylor, Aidan J. Farrell, Daniel P. Tzokov, Svetomir B. DiMaio, Frank Kelly, David J. Bergeron, Julien R. C. |
author_facet | Al-Otaibi, Natalie S. Taylor, Aidan J. Farrell, Daniel P. Tzokov, Svetomir B. DiMaio, Frank Kelly, David J. Bergeron, Julien R. C. |
author_sort | Al-Otaibi, Natalie S. |
collection | PubMed |
description | The bacterial flagellum is a remarkable molecular motor, whose primary function in bacteria is to facilitate motility through the rotation of a filament protruding from the bacterial cell. A cap complex, consisting of an oligomer of the protein FliD, is localized at the tip of the flagellum, and is essential for filament assembly, as well as adherence to surfaces in some bacteria. However, the structure of the intact cap complex, and the molecular basis for its interaction with the filament, remains elusive. Here we report the cryo-EM structure of the Campylobacter jejuni cap complex, which reveals that FliD is pentameric, with the N-terminal region of the protomer forming an extensive set of contacts across several subunits, that contribute to FliD oligomerization. We also demonstrate that the native C. jejuni flagellum filament is 11-stranded, contrary to a previously published cryo-EM structure, and propose a molecular model for the filament-cap interaction. |
format | Online Article Text |
id | pubmed-7316729 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-73167292020-06-30 The cryo-EM structure of the bacterial flagellum cap complex suggests a molecular mechanism for filament elongation Al-Otaibi, Natalie S. Taylor, Aidan J. Farrell, Daniel P. Tzokov, Svetomir B. DiMaio, Frank Kelly, David J. Bergeron, Julien R. C. Nat Commun Article The bacterial flagellum is a remarkable molecular motor, whose primary function in bacteria is to facilitate motility through the rotation of a filament protruding from the bacterial cell. A cap complex, consisting of an oligomer of the protein FliD, is localized at the tip of the flagellum, and is essential for filament assembly, as well as adherence to surfaces in some bacteria. However, the structure of the intact cap complex, and the molecular basis for its interaction with the filament, remains elusive. Here we report the cryo-EM structure of the Campylobacter jejuni cap complex, which reveals that FliD is pentameric, with the N-terminal region of the protomer forming an extensive set of contacts across several subunits, that contribute to FliD oligomerization. We also demonstrate that the native C. jejuni flagellum filament is 11-stranded, contrary to a previously published cryo-EM structure, and propose a molecular model for the filament-cap interaction. Nature Publishing Group UK 2020-06-25 /pmc/articles/PMC7316729/ /pubmed/32587243 http://dx.doi.org/10.1038/s41467-020-16981-4 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Al-Otaibi, Natalie S. Taylor, Aidan J. Farrell, Daniel P. Tzokov, Svetomir B. DiMaio, Frank Kelly, David J. Bergeron, Julien R. C. The cryo-EM structure of the bacterial flagellum cap complex suggests a molecular mechanism for filament elongation |
title | The cryo-EM structure of the bacterial flagellum cap complex suggests a molecular mechanism for filament elongation |
title_full | The cryo-EM structure of the bacterial flagellum cap complex suggests a molecular mechanism for filament elongation |
title_fullStr | The cryo-EM structure of the bacterial flagellum cap complex suggests a molecular mechanism for filament elongation |
title_full_unstemmed | The cryo-EM structure of the bacterial flagellum cap complex suggests a molecular mechanism for filament elongation |
title_short | The cryo-EM structure of the bacterial flagellum cap complex suggests a molecular mechanism for filament elongation |
title_sort | cryo-em structure of the bacterial flagellum cap complex suggests a molecular mechanism for filament elongation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7316729/ https://www.ncbi.nlm.nih.gov/pubmed/32587243 http://dx.doi.org/10.1038/s41467-020-16981-4 |
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