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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
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.
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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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