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Actin Crosslinking Toxins of Gram-Negative Bacteria

Actin crosslinking toxins produced by Gram-negative bacteria represent a small but unique class of bacterial protein toxins. For each of these toxins, a discrete actin crosslinking domain (ACD) that is a distant member of the ATP-dependent glutamine synthetase family of protein ligases is translocat...

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Autor principal: Satchell, Karla J. F.
Formato: Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2908040/
https://www.ncbi.nlm.nih.gov/pubmed/20651954
http://dx.doi.org/10.3390/toxins1020123
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author Satchell, Karla J. F.
author_facet Satchell, Karla J. F.
author_sort Satchell, Karla J. F.
collection PubMed
description Actin crosslinking toxins produced by Gram-negative bacteria represent a small but unique class of bacterial protein toxins. For each of these toxins, a discrete actin crosslinking domain (ACD) that is a distant member of the ATP-dependent glutamine synthetase family of protein ligases is translocated to the eukaryotic cell cytosol. This domain then incorporates a glutamate-lysine crosslink between actin monomers, resulting in destruction of the actin cytoskeleton. Recent studies argue that the function of these toxins during infection is not destruction of epithelial layers, but rather may specifically target phagocytic cells to promote survival of bacteria after the onset of innate immune defenses. This review will summarize key experiments performed over the past 10 years to reveal the function of these toxins.
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spelling pubmed-29080402010-07-21 Actin Crosslinking Toxins of Gram-Negative Bacteria Satchell, Karla J. F. Toxins (Basel) Review Actin crosslinking toxins produced by Gram-negative bacteria represent a small but unique class of bacterial protein toxins. For each of these toxins, a discrete actin crosslinking domain (ACD) that is a distant member of the ATP-dependent glutamine synthetase family of protein ligases is translocated to the eukaryotic cell cytosol. This domain then incorporates a glutamate-lysine crosslink between actin monomers, resulting in destruction of the actin cytoskeleton. Recent studies argue that the function of these toxins during infection is not destruction of epithelial layers, but rather may specifically target phagocytic cells to promote survival of bacteria after the onset of innate immune defenses. This review will summarize key experiments performed over the past 10 years to reveal the function of these toxins. Molecular Diversity Preservation International 2009-12-01 /pmc/articles/PMC2908040/ /pubmed/20651954 http://dx.doi.org/10.3390/toxins1020123 Text en © 2009 by the authors; licensee Molecular Diversity Preservation International, Basel, Switzerland http://creativecommons.org/licenses/by/3.0/ This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Review
Satchell, Karla J. F.
Actin Crosslinking Toxins of Gram-Negative Bacteria
title Actin Crosslinking Toxins of Gram-Negative Bacteria
title_full Actin Crosslinking Toxins of Gram-Negative Bacteria
title_fullStr Actin Crosslinking Toxins of Gram-Negative Bacteria
title_full_unstemmed Actin Crosslinking Toxins of Gram-Negative Bacteria
title_short Actin Crosslinking Toxins of Gram-Negative Bacteria
title_sort actin crosslinking toxins of gram-negative bacteria
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2908040/
https://www.ncbi.nlm.nih.gov/pubmed/20651954
http://dx.doi.org/10.3390/toxins1020123
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