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Investigations on the mode of action of gephyronic acid, an inhibitor of eukaryotic protein translation from myxobacteria
The identification of inhibitors of eukaryotic protein biosynthesis, which are targeting single translation factors, is highly demanded. Here we report on a small molecule inhibitor, gephyronic acid, isolated from the myxobacterium Archangium gephyra that inhibits growth of transformed mammalian cel...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6067752/ https://www.ncbi.nlm.nih.gov/pubmed/30063768 http://dx.doi.org/10.1371/journal.pone.0201605 |
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author | Muthukumar, Yazh Münkemer, Johanna Mathieu, Daniel Richter, Christian Schwalbe, Harald Steinmetz, Heinrich Kessler, Wolfgang Reichelt, Joachim Beutling, Ulrike Frank, Ronald Büssow, Konrad van den Heuvel, Joop Brönstrup, Mark Taylor, Richard E. Laschat, Sabine Sasse, Florenz |
author_facet | Muthukumar, Yazh Münkemer, Johanna Mathieu, Daniel Richter, Christian Schwalbe, Harald Steinmetz, Heinrich Kessler, Wolfgang Reichelt, Joachim Beutling, Ulrike Frank, Ronald Büssow, Konrad van den Heuvel, Joop Brönstrup, Mark Taylor, Richard E. Laschat, Sabine Sasse, Florenz |
author_sort | Muthukumar, Yazh |
collection | PubMed |
description | The identification of inhibitors of eukaryotic protein biosynthesis, which are targeting single translation factors, is highly demanded. Here we report on a small molecule inhibitor, gephyronic acid, isolated from the myxobacterium Archangium gephyra that inhibits growth of transformed mammalian cell lines in the nM range. In direct comparison, primary human fibroblasts were shown to be less sensitive to toxic effects of gephyronic acid than cancer-derived cells. Gephyronic acid is targeting the protein translation system. Experiments with IRES dual luciferase reporter assays identified it as an inhibitor of the translation initiation. DARTs approaches, co-localization studies and pull-down assays indicate that the binding partner could be the eukaryotic initiation factor 2 subunit alpha (eIF2α). Gephyronic acid seems to have a different mode of action than the structurally related polyketides tedanolide, myriaporone, and pederin and is a valuable tool for investigating the eukaryotic translation system. Because cancer derived cells were found to be especially sensitive, gephyronic acid could potentially find use as a drug candidate. |
format | Online Article Text |
id | pubmed-6067752 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-60677522018-08-10 Investigations on the mode of action of gephyronic acid, an inhibitor of eukaryotic protein translation from myxobacteria Muthukumar, Yazh Münkemer, Johanna Mathieu, Daniel Richter, Christian Schwalbe, Harald Steinmetz, Heinrich Kessler, Wolfgang Reichelt, Joachim Beutling, Ulrike Frank, Ronald Büssow, Konrad van den Heuvel, Joop Brönstrup, Mark Taylor, Richard E. Laschat, Sabine Sasse, Florenz PLoS One Research Article The identification of inhibitors of eukaryotic protein biosynthesis, which are targeting single translation factors, is highly demanded. Here we report on a small molecule inhibitor, gephyronic acid, isolated from the myxobacterium Archangium gephyra that inhibits growth of transformed mammalian cell lines in the nM range. In direct comparison, primary human fibroblasts were shown to be less sensitive to toxic effects of gephyronic acid than cancer-derived cells. Gephyronic acid is targeting the protein translation system. Experiments with IRES dual luciferase reporter assays identified it as an inhibitor of the translation initiation. DARTs approaches, co-localization studies and pull-down assays indicate that the binding partner could be the eukaryotic initiation factor 2 subunit alpha (eIF2α). Gephyronic acid seems to have a different mode of action than the structurally related polyketides tedanolide, myriaporone, and pederin and is a valuable tool for investigating the eukaryotic translation system. Because cancer derived cells were found to be especially sensitive, gephyronic acid could potentially find use as a drug candidate. Public Library of Science 2018-07-31 /pmc/articles/PMC6067752/ /pubmed/30063768 http://dx.doi.org/10.1371/journal.pone.0201605 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 Muthukumar, Yazh Münkemer, Johanna Mathieu, Daniel Richter, Christian Schwalbe, Harald Steinmetz, Heinrich Kessler, Wolfgang Reichelt, Joachim Beutling, Ulrike Frank, Ronald Büssow, Konrad van den Heuvel, Joop Brönstrup, Mark Taylor, Richard E. Laschat, Sabine Sasse, Florenz Investigations on the mode of action of gephyronic acid, an inhibitor of eukaryotic protein translation from myxobacteria |
title | Investigations on the mode of action of gephyronic acid, an inhibitor of eukaryotic protein translation from myxobacteria |
title_full | Investigations on the mode of action of gephyronic acid, an inhibitor of eukaryotic protein translation from myxobacteria |
title_fullStr | Investigations on the mode of action of gephyronic acid, an inhibitor of eukaryotic protein translation from myxobacteria |
title_full_unstemmed | Investigations on the mode of action of gephyronic acid, an inhibitor of eukaryotic protein translation from myxobacteria |
title_short | Investigations on the mode of action of gephyronic acid, an inhibitor of eukaryotic protein translation from myxobacteria |
title_sort | investigations on the mode of action of gephyronic acid, an inhibitor of eukaryotic protein translation from myxobacteria |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6067752/ https://www.ncbi.nlm.nih.gov/pubmed/30063768 http://dx.doi.org/10.1371/journal.pone.0201605 |
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