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The natural product carolacton inhibits folate-dependent C1 metabolism by targeting FolD/MTHFD
The natural product carolacton is a macrolide keto-carboxylic acid produced by the myxobacterium Sorangium cellulosum, and was originally described as an antibacterial compound. Here we show that carolacton targets FolD, a key enzyme from the folate-dependent C1 metabolism. We characterize the inter...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5688156/ https://www.ncbi.nlm.nih.gov/pubmed/29142318 http://dx.doi.org/10.1038/s41467-017-01671-5 |
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author | Fu, Chengzhang Sikandar, Asfandyar Donner, Jannik Zaburannyi, Nestor Herrmann, Jennifer Reck, Michael Wagner-Döbler, Irene Koehnke, Jesko Müller, Rolf |
author_facet | Fu, Chengzhang Sikandar, Asfandyar Donner, Jannik Zaburannyi, Nestor Herrmann, Jennifer Reck, Michael Wagner-Döbler, Irene Koehnke, Jesko Müller, Rolf |
author_sort | Fu, Chengzhang |
collection | PubMed |
description | The natural product carolacton is a macrolide keto-carboxylic acid produced by the myxobacterium Sorangium cellulosum, and was originally described as an antibacterial compound. Here we show that carolacton targets FolD, a key enzyme from the folate-dependent C1 metabolism. We characterize the interaction between bacterial FolD and carolacton biophysically, structurally and biochemically. Carolacton binds FolD with nanomolar affinity, and the crystal structure of the FolD–carolacton complex reveals the mode of binding. We show that the human FolD orthologs, MTHFD1 and MTHFD2, are also inhibited in the low nM range, and that micromolar concentrations of carolacton inhibit the growth of cancer cell lines. As mitochondrial MTHFD2 is known to be upregulated in cancer cells, it may be possible to use carolacton as an inhibitor tool compound to assess MTHFD2 as an anti-cancer target. |
format | Online Article Text |
id | pubmed-5688156 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-56881562017-11-17 The natural product carolacton inhibits folate-dependent C1 metabolism by targeting FolD/MTHFD Fu, Chengzhang Sikandar, Asfandyar Donner, Jannik Zaburannyi, Nestor Herrmann, Jennifer Reck, Michael Wagner-Döbler, Irene Koehnke, Jesko Müller, Rolf Nat Commun Article The natural product carolacton is a macrolide keto-carboxylic acid produced by the myxobacterium Sorangium cellulosum, and was originally described as an antibacterial compound. Here we show that carolacton targets FolD, a key enzyme from the folate-dependent C1 metabolism. We characterize the interaction between bacterial FolD and carolacton biophysically, structurally and biochemically. Carolacton binds FolD with nanomolar affinity, and the crystal structure of the FolD–carolacton complex reveals the mode of binding. We show that the human FolD orthologs, MTHFD1 and MTHFD2, are also inhibited in the low nM range, and that micromolar concentrations of carolacton inhibit the growth of cancer cell lines. As mitochondrial MTHFD2 is known to be upregulated in cancer cells, it may be possible to use carolacton as an inhibitor tool compound to assess MTHFD2 as an anti-cancer target. Nature Publishing Group UK 2017-11-16 /pmc/articles/PMC5688156/ /pubmed/29142318 http://dx.doi.org/10.1038/s41467-017-01671-5 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Fu, Chengzhang Sikandar, Asfandyar Donner, Jannik Zaburannyi, Nestor Herrmann, Jennifer Reck, Michael Wagner-Döbler, Irene Koehnke, Jesko Müller, Rolf The natural product carolacton inhibits folate-dependent C1 metabolism by targeting FolD/MTHFD |
title | The natural product carolacton inhibits folate-dependent C1 metabolism by targeting FolD/MTHFD |
title_full | The natural product carolacton inhibits folate-dependent C1 metabolism by targeting FolD/MTHFD |
title_fullStr | The natural product carolacton inhibits folate-dependent C1 metabolism by targeting FolD/MTHFD |
title_full_unstemmed | The natural product carolacton inhibits folate-dependent C1 metabolism by targeting FolD/MTHFD |
title_short | The natural product carolacton inhibits folate-dependent C1 metabolism by targeting FolD/MTHFD |
title_sort | natural product carolacton inhibits folate-dependent c1 metabolism by targeting fold/mthfd |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5688156/ https://www.ncbi.nlm.nih.gov/pubmed/29142318 http://dx.doi.org/10.1038/s41467-017-01671-5 |
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