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In situ structural analysis of the Yersinia enterocolitica injectisome
Injectisomes are multi-protein transmembrane machines allowing pathogenic bacteria to inject effector proteins into eukaryotic host cells, a process called type III secretion. Here we present the first three-dimensional structure of Yersinia enterocolitica and Shigella flexneri injectisomes in situ...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3728920/ https://www.ncbi.nlm.nih.gov/pubmed/23908767 http://dx.doi.org/10.7554/eLife.00792 |
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author | Kudryashev, Mikhail Stenta, Marco Schmelz, Stefan Amstutz, Marlise Wiesand, Ulrich Castaño-Díez, Daniel Degiacomi, Matteo T Münnich, Stefan Bleck, Christopher KE Kowal, Julia Diepold, Andreas Heinz, Dirk W Dal Peraro, Matteo Cornelis, Guy R Stahlberg, Henning |
author_facet | Kudryashev, Mikhail Stenta, Marco Schmelz, Stefan Amstutz, Marlise Wiesand, Ulrich Castaño-Díez, Daniel Degiacomi, Matteo T Münnich, Stefan Bleck, Christopher KE Kowal, Julia Diepold, Andreas Heinz, Dirk W Dal Peraro, Matteo Cornelis, Guy R Stahlberg, Henning |
author_sort | Kudryashev, Mikhail |
collection | PubMed |
description | Injectisomes are multi-protein transmembrane machines allowing pathogenic bacteria to inject effector proteins into eukaryotic host cells, a process called type III secretion. Here we present the first three-dimensional structure of Yersinia enterocolitica and Shigella flexneri injectisomes in situ and the first structural analysis of the Yersinia injectisome. Unexpectedly, basal bodies of injectisomes inside the bacterial cells showed length variations of 20%. The in situ structures of the Y. enterocolitica and S. flexneri injectisomes had similar dimensions and were significantly longer than the isolated structures of related injectisomes. The crystal structure of the inner membrane injectisome component YscD appeared elongated compared to a homologous protein, and molecular dynamics simulations documented its elongation elasticity. The ring-shaped secretin YscC at the outer membrane was stretched by 30–40% in situ, compared to its isolated liposome-embedded conformation. We suggest that elasticity is critical for some two-membrane spanning protein complexes to cope with variations in the intermembrane distance. DOI: http://dx.doi.org/10.7554/eLife.00792.001 |
format | Online Article Text |
id | pubmed-3728920 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-37289202013-08-01 In situ structural analysis of the Yersinia enterocolitica injectisome Kudryashev, Mikhail Stenta, Marco Schmelz, Stefan Amstutz, Marlise Wiesand, Ulrich Castaño-Díez, Daniel Degiacomi, Matteo T Münnich, Stefan Bleck, Christopher KE Kowal, Julia Diepold, Andreas Heinz, Dirk W Dal Peraro, Matteo Cornelis, Guy R Stahlberg, Henning eLife Biophysics and Structural Biology Injectisomes are multi-protein transmembrane machines allowing pathogenic bacteria to inject effector proteins into eukaryotic host cells, a process called type III secretion. Here we present the first three-dimensional structure of Yersinia enterocolitica and Shigella flexneri injectisomes in situ and the first structural analysis of the Yersinia injectisome. Unexpectedly, basal bodies of injectisomes inside the bacterial cells showed length variations of 20%. The in situ structures of the Y. enterocolitica and S. flexneri injectisomes had similar dimensions and were significantly longer than the isolated structures of related injectisomes. The crystal structure of the inner membrane injectisome component YscD appeared elongated compared to a homologous protein, and molecular dynamics simulations documented its elongation elasticity. The ring-shaped secretin YscC at the outer membrane was stretched by 30–40% in situ, compared to its isolated liposome-embedded conformation. We suggest that elasticity is critical for some two-membrane spanning protein complexes to cope with variations in the intermembrane distance. DOI: http://dx.doi.org/10.7554/eLife.00792.001 eLife Sciences Publications, Ltd 2013-07-30 /pmc/articles/PMC3728920/ /pubmed/23908767 http://dx.doi.org/10.7554/eLife.00792 Text en Copyright © 2013, Kudryashev et al http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Biophysics and Structural Biology Kudryashev, Mikhail Stenta, Marco Schmelz, Stefan Amstutz, Marlise Wiesand, Ulrich Castaño-Díez, Daniel Degiacomi, Matteo T Münnich, Stefan Bleck, Christopher KE Kowal, Julia Diepold, Andreas Heinz, Dirk W Dal Peraro, Matteo Cornelis, Guy R Stahlberg, Henning In situ structural analysis of the Yersinia enterocolitica injectisome |
title | In situ structural analysis of the Yersinia
enterocolitica injectisome |
title_full | In situ structural analysis of the Yersinia
enterocolitica injectisome |
title_fullStr | In situ structural analysis of the Yersinia
enterocolitica injectisome |
title_full_unstemmed | In situ structural analysis of the Yersinia
enterocolitica injectisome |
title_short | In situ structural analysis of the Yersinia
enterocolitica injectisome |
title_sort | in situ structural analysis of the yersinia
enterocolitica injectisome |
topic | Biophysics and Structural Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3728920/ https://www.ncbi.nlm.nih.gov/pubmed/23908767 http://dx.doi.org/10.7554/eLife.00792 |
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