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Stable Isotope-Assisted Metabolomics for Deciphering Xenobiotic Metabolism in Mammalian Cell Culture
[Image: see text] Xenobiotics are ubiquitous in the environment and modified in the human body by phase I and II metabolism. Liquid chromatography coupled to high resolution mass spectrometry is a powerful tool to investigate these biotransformation products. We present a workflow based on stable is...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7171601/ https://www.ncbi.nlm.nih.gov/pubmed/32167285 http://dx.doi.org/10.1021/acschembio.9b01016 |
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author | Flasch, Mira Bueschl, Christoph Woelflingseder, Lydia Schwartz-Zimmermann, Heidi E. Adam, Gerhard Schuhmacher, Rainer Marko, Doris Warth, Benedikt |
author_facet | Flasch, Mira Bueschl, Christoph Woelflingseder, Lydia Schwartz-Zimmermann, Heidi E. Adam, Gerhard Schuhmacher, Rainer Marko, Doris Warth, Benedikt |
author_sort | Flasch, Mira |
collection | PubMed |
description | [Image: see text] Xenobiotics are ubiquitous in the environment and modified in the human body by phase I and II metabolism. Liquid chromatography coupled to high resolution mass spectrometry is a powerful tool to investigate these biotransformation products. We present a workflow based on stable isotope-assisted metabolomics and the bioinformatics tool MetExtract II for deciphering xenobiotic metabolites produced by human cells. Its potential was demonstrated by the investigation of the metabolism of deoxynivalenol (DON), an abundant food contaminant, in a liver carcinoma cell line (HepG2) and a model for colon carcinoma (HT29). Detected known metabolites included DON-3-sulfate, DON-10-sulfonate 2, and DON-10-glutathione as well as DON-cysteine. Conjugation with amino acids and an antibiotic was confirmed for the first time. The approach allows the untargeted elucidation of human xenobiotic products in tissue culture. It may be applied to other fields of research including drug metabolism, personalized medicine, exposome research, and systems biology to better understand the relevance of in vitro experiments. |
format | Online Article Text |
id | pubmed-7171601 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-71716012020-04-21 Stable Isotope-Assisted Metabolomics for Deciphering Xenobiotic Metabolism in Mammalian Cell Culture Flasch, Mira Bueschl, Christoph Woelflingseder, Lydia Schwartz-Zimmermann, Heidi E. Adam, Gerhard Schuhmacher, Rainer Marko, Doris Warth, Benedikt ACS Chem Biol [Image: see text] Xenobiotics are ubiquitous in the environment and modified in the human body by phase I and II metabolism. Liquid chromatography coupled to high resolution mass spectrometry is a powerful tool to investigate these biotransformation products. We present a workflow based on stable isotope-assisted metabolomics and the bioinformatics tool MetExtract II for deciphering xenobiotic metabolites produced by human cells. Its potential was demonstrated by the investigation of the metabolism of deoxynivalenol (DON), an abundant food contaminant, in a liver carcinoma cell line (HepG2) and a model for colon carcinoma (HT29). Detected known metabolites included DON-3-sulfate, DON-10-sulfonate 2, and DON-10-glutathione as well as DON-cysteine. Conjugation with amino acids and an antibiotic was confirmed for the first time. The approach allows the untargeted elucidation of human xenobiotic products in tissue culture. It may be applied to other fields of research including drug metabolism, personalized medicine, exposome research, and systems biology to better understand the relevance of in vitro experiments. American Chemical Society 2020-03-13 2020-04-17 /pmc/articles/PMC7171601/ /pubmed/32167285 http://dx.doi.org/10.1021/acschembio.9b01016 Text en Copyright © 2020 American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited. |
spellingShingle | Flasch, Mira Bueschl, Christoph Woelflingseder, Lydia Schwartz-Zimmermann, Heidi E. Adam, Gerhard Schuhmacher, Rainer Marko, Doris Warth, Benedikt Stable Isotope-Assisted Metabolomics for Deciphering Xenobiotic Metabolism in Mammalian Cell Culture |
title | Stable Isotope-Assisted Metabolomics for Deciphering
Xenobiotic Metabolism in Mammalian Cell Culture |
title_full | Stable Isotope-Assisted Metabolomics for Deciphering
Xenobiotic Metabolism in Mammalian Cell Culture |
title_fullStr | Stable Isotope-Assisted Metabolomics for Deciphering
Xenobiotic Metabolism in Mammalian Cell Culture |
title_full_unstemmed | Stable Isotope-Assisted Metabolomics for Deciphering
Xenobiotic Metabolism in Mammalian Cell Culture |
title_short | Stable Isotope-Assisted Metabolomics for Deciphering
Xenobiotic Metabolism in Mammalian Cell Culture |
title_sort | stable isotope-assisted metabolomics for deciphering
xenobiotic metabolism in mammalian cell culture |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7171601/ https://www.ncbi.nlm.nih.gov/pubmed/32167285 http://dx.doi.org/10.1021/acschembio.9b01016 |
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