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Cryo-EM analysis of the T3S injectisome reveals the structure of the needle and open secretin
The bacterial type III secretion system, or injectisome, is a syringe shaped nanomachine essential for the virulence of many disease causing Gram-negative bacteria. At the core of the injectisome structure is the needle complex, a continuous channel formed by the highly oligomerized inner and outer...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6155069/ https://www.ncbi.nlm.nih.gov/pubmed/30242280 http://dx.doi.org/10.1038/s41467-018-06298-8 |
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author | Hu, J. Worrall, L. J. Hong, C. Vuckovic, M. Atkinson, C. E. Caveney, N. Yu, Z. Strynadka, N. C. J. |
author_facet | Hu, J. Worrall, L. J. Hong, C. Vuckovic, M. Atkinson, C. E. Caveney, N. Yu, Z. Strynadka, N. C. J. |
author_sort | Hu, J. |
collection | PubMed |
description | The bacterial type III secretion system, or injectisome, is a syringe shaped nanomachine essential for the virulence of many disease causing Gram-negative bacteria. At the core of the injectisome structure is the needle complex, a continuous channel formed by the highly oligomerized inner and outer membrane hollow rings and a polymerized helical needle filament which spans through and projects into the infected host cell. Here we present the near-atomic resolution structure of a needle complex from the prototypical Salmonella Typhimurium SPI-1 type III secretion system, with local masking protocols allowing for model building and refinement of the major membrane spanning components of the needle complex base in addition to an isolated needle filament. This work provides significant insight into injectisome structure and assembly and importantly captures the molecular basis for substrate induced gating in the giant outer membrane secretin portal family. |
format | Online Article Text |
id | pubmed-6155069 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-61550692018-09-28 Cryo-EM analysis of the T3S injectisome reveals the structure of the needle and open secretin Hu, J. Worrall, L. J. Hong, C. Vuckovic, M. Atkinson, C. E. Caveney, N. Yu, Z. Strynadka, N. C. J. Nat Commun Article The bacterial type III secretion system, or injectisome, is a syringe shaped nanomachine essential for the virulence of many disease causing Gram-negative bacteria. At the core of the injectisome structure is the needle complex, a continuous channel formed by the highly oligomerized inner and outer membrane hollow rings and a polymerized helical needle filament which spans through and projects into the infected host cell. Here we present the near-atomic resolution structure of a needle complex from the prototypical Salmonella Typhimurium SPI-1 type III secretion system, with local masking protocols allowing for model building and refinement of the major membrane spanning components of the needle complex base in addition to an isolated needle filament. This work provides significant insight into injectisome structure and assembly and importantly captures the molecular basis for substrate induced gating in the giant outer membrane secretin portal family. Nature Publishing Group UK 2018-09-21 /pmc/articles/PMC6155069/ /pubmed/30242280 http://dx.doi.org/10.1038/s41467-018-06298-8 Text en © The Author(s) 2018 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 Hu, J. Worrall, L. J. Hong, C. Vuckovic, M. Atkinson, C. E. Caveney, N. Yu, Z. Strynadka, N. C. J. Cryo-EM analysis of the T3S injectisome reveals the structure of the needle and open secretin |
title | Cryo-EM analysis of the T3S injectisome reveals the structure of the needle and open secretin |
title_full | Cryo-EM analysis of the T3S injectisome reveals the structure of the needle and open secretin |
title_fullStr | Cryo-EM analysis of the T3S injectisome reveals the structure of the needle and open secretin |
title_full_unstemmed | Cryo-EM analysis of the T3S injectisome reveals the structure of the needle and open secretin |
title_short | Cryo-EM analysis of the T3S injectisome reveals the structure of the needle and open secretin |
title_sort | cryo-em analysis of the t3s injectisome reveals the structure of the needle and open secretin |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6155069/ https://www.ncbi.nlm.nih.gov/pubmed/30242280 http://dx.doi.org/10.1038/s41467-018-06298-8 |
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