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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2013
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
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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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