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Cell entry machines: a common theme in nature?

Molecular machines orchestrate the translocation and entry of pathogens through host cell membranes, in addition to the uptake and release of molecules during endocytosis and exocytosis. Viral cell entry requires a family of glycoproteins, and the structural organization and function of these viral...

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Autores principales: Barocchi, Michèle A., Masignani, Vega, Rappuoli, Rino
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7097853/
https://www.ncbi.nlm.nih.gov/pubmed/15759040
http://dx.doi.org/10.1038/nrmicro1131
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author Barocchi, Michèle A.
Masignani, Vega
Rappuoli, Rino
author_facet Barocchi, Michèle A.
Masignani, Vega
Rappuoli, Rino
author_sort Barocchi, Michèle A.
collection PubMed
description Molecular machines orchestrate the translocation and entry of pathogens through host cell membranes, in addition to the uptake and release of molecules during endocytosis and exocytosis. Viral cell entry requires a family of glycoproteins, and the structural organization and function of these viral glycoproteins are similar to the SNARE proteins, which are known to be involved in intracellular vesicle fusion, endocytosis and exocytosis. Here, we propose that a family of bacterial membrane proteins that are responsible for cell-mediated adherence and entry resembles the structural architecture of both viral fusion proteins and eukaryotic SNAREs and might therefore share similar, but distinct, mechanisms of cell membrane translocation. Furthermore, we propose that the recurrence of these molecular machines across species indicates that these architectural motifs were evolutionarily selected because they provided the best solution to ensure the survival of pathogens within a particular environment.
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spelling pubmed-70978532020-03-26 Cell entry machines: a common theme in nature? Barocchi, Michèle A. Masignani, Vega Rappuoli, Rino Nat Rev Microbiol Article Molecular machines orchestrate the translocation and entry of pathogens through host cell membranes, in addition to the uptake and release of molecules during endocytosis and exocytosis. Viral cell entry requires a family of glycoproteins, and the structural organization and function of these viral glycoproteins are similar to the SNARE proteins, which are known to be involved in intracellular vesicle fusion, endocytosis and exocytosis. Here, we propose that a family of bacterial membrane proteins that are responsible for cell-mediated adherence and entry resembles the structural architecture of both viral fusion proteins and eukaryotic SNAREs and might therefore share similar, but distinct, mechanisms of cell membrane translocation. Furthermore, we propose that the recurrence of these molecular machines across species indicates that these architectural motifs were evolutionarily selected because they provided the best solution to ensure the survival of pathogens within a particular environment. Nature Publishing Group UK 2005-03-10 2005 /pmc/articles/PMC7097853/ /pubmed/15759040 http://dx.doi.org/10.1038/nrmicro1131 Text en © Nature Publishing Group 2005 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Article
Barocchi, Michèle A.
Masignani, Vega
Rappuoli, Rino
Cell entry machines: a common theme in nature?
title Cell entry machines: a common theme in nature?
title_full Cell entry machines: a common theme in nature?
title_fullStr Cell entry machines: a common theme in nature?
title_full_unstemmed Cell entry machines: a common theme in nature?
title_short Cell entry machines: a common theme in nature?
title_sort cell entry machines: a common theme in nature?
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7097853/
https://www.ncbi.nlm.nih.gov/pubmed/15759040
http://dx.doi.org/10.1038/nrmicro1131
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