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Inhibition of Cholera Toxin and Other AB Toxins by Polyphenolic Compounds
Cholera toxin (CT) is an AB-type protein toxin that contains a catalytic A1 subunit, an A2 linker, and a cell-binding B homopentamer. The CT holotoxin is released into the extracellular environment, but CTA1 attacks a target within the cytosol of a host cell. We recently reported that grape extract...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5102367/ https://www.ncbi.nlm.nih.gov/pubmed/27829022 http://dx.doi.org/10.1371/journal.pone.0166477 |
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author | Cherubin, Patrick Garcia, Maria Camila Curtis, David Britt, Christopher B. T. Craft, John W. Burress, Helen Berndt, Chris Reddy, Srikar Guyette, Jessica Zheng, Tianyu Huo, Qun Quiñones, Beatriz Briggs, James M. Teter, Ken |
author_facet | Cherubin, Patrick Garcia, Maria Camila Curtis, David Britt, Christopher B. T. Craft, John W. Burress, Helen Berndt, Chris Reddy, Srikar Guyette, Jessica Zheng, Tianyu Huo, Qun Quiñones, Beatriz Briggs, James M. Teter, Ken |
author_sort | Cherubin, Patrick |
collection | PubMed |
description | Cholera toxin (CT) is an AB-type protein toxin that contains a catalytic A1 subunit, an A2 linker, and a cell-binding B homopentamer. The CT holotoxin is released into the extracellular environment, but CTA1 attacks a target within the cytosol of a host cell. We recently reported that grape extract confers substantial resistance to CT. Here, we used a cell culture system to identify twelve individual phenolic compounds from grape extract that inhibit CT. Additional studies determined the mechanism of inhibition for a subset of the compounds: two inhibited CT binding to the cell surface and even stripped CT from the plasma membrane of a target cell; two inhibited the enzymatic activity of CTA1; and four blocked cytosolic toxin activity without directly affecting the enzymatic function of CTA1. Individual polyphenolic compounds from grape extract could also generate cellular resistance to diphtheria toxin, exotoxin A, and ricin. We have thus identified individual toxin inhibitors from grape extract and some of their mechanisms of inhibition against CT. |
format | Online Article Text |
id | pubmed-5102367 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-51023672016-11-18 Inhibition of Cholera Toxin and Other AB Toxins by Polyphenolic Compounds Cherubin, Patrick Garcia, Maria Camila Curtis, David Britt, Christopher B. T. Craft, John W. Burress, Helen Berndt, Chris Reddy, Srikar Guyette, Jessica Zheng, Tianyu Huo, Qun Quiñones, Beatriz Briggs, James M. Teter, Ken PLoS One Research Article Cholera toxin (CT) is an AB-type protein toxin that contains a catalytic A1 subunit, an A2 linker, and a cell-binding B homopentamer. The CT holotoxin is released into the extracellular environment, but CTA1 attacks a target within the cytosol of a host cell. We recently reported that grape extract confers substantial resistance to CT. Here, we used a cell culture system to identify twelve individual phenolic compounds from grape extract that inhibit CT. Additional studies determined the mechanism of inhibition for a subset of the compounds: two inhibited CT binding to the cell surface and even stripped CT from the plasma membrane of a target cell; two inhibited the enzymatic activity of CTA1; and four blocked cytosolic toxin activity without directly affecting the enzymatic function of CTA1. Individual polyphenolic compounds from grape extract could also generate cellular resistance to diphtheria toxin, exotoxin A, and ricin. We have thus identified individual toxin inhibitors from grape extract and some of their mechanisms of inhibition against CT. Public Library of Science 2016-11-09 /pmc/articles/PMC5102367/ /pubmed/27829022 http://dx.doi.org/10.1371/journal.pone.0166477 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication. |
spellingShingle | Research Article Cherubin, Patrick Garcia, Maria Camila Curtis, David Britt, Christopher B. T. Craft, John W. Burress, Helen Berndt, Chris Reddy, Srikar Guyette, Jessica Zheng, Tianyu Huo, Qun Quiñones, Beatriz Briggs, James M. Teter, Ken Inhibition of Cholera Toxin and Other AB Toxins by Polyphenolic Compounds |
title | Inhibition of Cholera Toxin and Other AB Toxins by Polyphenolic Compounds |
title_full | Inhibition of Cholera Toxin and Other AB Toxins by Polyphenolic Compounds |
title_fullStr | Inhibition of Cholera Toxin and Other AB Toxins by Polyphenolic Compounds |
title_full_unstemmed | Inhibition of Cholera Toxin and Other AB Toxins by Polyphenolic Compounds |
title_short | Inhibition of Cholera Toxin and Other AB Toxins by Polyphenolic Compounds |
title_sort | inhibition of cholera toxin and other ab toxins by polyphenolic compounds |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5102367/ https://www.ncbi.nlm.nih.gov/pubmed/27829022 http://dx.doi.org/10.1371/journal.pone.0166477 |
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