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Cryo-EM of the injectisome and type III secretion systems

Double-membrane-spanning protein complexes, such as the T3SS, had long presented an intractable challenge for structural biology. As a consequence, until a few years ago, our molecular understanding of this fascinating complex was limited to composite models, consisting of structures of isolated dom...

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Detalles Bibliográficos
Autores principales: Bergeron, Julien R.C., Marlovits, Thomas C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10114087/
https://www.ncbi.nlm.nih.gov/pubmed/35724552
http://dx.doi.org/10.1016/j.sbi.2022.102403
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author Bergeron, Julien R.C.
Marlovits, Thomas C.
author_facet Bergeron, Julien R.C.
Marlovits, Thomas C.
author_sort Bergeron, Julien R.C.
collection PubMed
description Double-membrane-spanning protein complexes, such as the T3SS, had long presented an intractable challenge for structural biology. As a consequence, until a few years ago, our molecular understanding of this fascinating complex was limited to composite models, consisting of structures of isolated domains, positioned within the overall complex. Most of the membrane-embedded components remained completely uncharacterized. In recent years, the emergence of cryo-electron microscopy (cryo-EM) as a method for determining protein structures to high resolution, has be transformative to our capacity to understand the architecture of this complex, and its mechanism of substrate transport. In this review, we summarize the recent structures of the various T3SS components, determined by cryo-EM, and highlight the regions of the complex that remain to be characterized. We also discuss the recent structural insights into the mechanism of effector transport through the T3SS. Finally, we highlight some of the challenges that remain to be tackled.
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spelling pubmed-101140872023-04-20 Cryo-EM of the injectisome and type III secretion systems Bergeron, Julien R.C. Marlovits, Thomas C. Curr Opin Struct Biol Article Double-membrane-spanning protein complexes, such as the T3SS, had long presented an intractable challenge for structural biology. As a consequence, until a few years ago, our molecular understanding of this fascinating complex was limited to composite models, consisting of structures of isolated domains, positioned within the overall complex. Most of the membrane-embedded components remained completely uncharacterized. In recent years, the emergence of cryo-electron microscopy (cryo-EM) as a method for determining protein structures to high resolution, has be transformative to our capacity to understand the architecture of this complex, and its mechanism of substrate transport. In this review, we summarize the recent structures of the various T3SS components, determined by cryo-EM, and highlight the regions of the complex that remain to be characterized. We also discuss the recent structural insights into the mechanism of effector transport through the T3SS. Finally, we highlight some of the challenges that remain to be tackled. Elsevier Science 2022-08 /pmc/articles/PMC10114087/ /pubmed/35724552 http://dx.doi.org/10.1016/j.sbi.2022.102403 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Bergeron, Julien R.C.
Marlovits, Thomas C.
Cryo-EM of the injectisome and type III secretion systems
title Cryo-EM of the injectisome and type III secretion systems
title_full Cryo-EM of the injectisome and type III secretion systems
title_fullStr Cryo-EM of the injectisome and type III secretion systems
title_full_unstemmed Cryo-EM of the injectisome and type III secretion systems
title_short Cryo-EM of the injectisome and type III secretion systems
title_sort cryo-em of the injectisome and type iii secretion systems
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10114087/
https://www.ncbi.nlm.nih.gov/pubmed/35724552
http://dx.doi.org/10.1016/j.sbi.2022.102403
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