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Comparative metabolomics with Metaboseek reveals functions of a conserved fat metabolism pathway in C. elegans
Untargeted metabolomics via high-resolution mass spectrometry can reveal more than 100,000 molecular features in a single sample, many of which may represent unidentified metabolites, posing significant challenges to data analysis. We here introduce Metaboseek, an open-source analysis platform desig...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8831614/ https://www.ncbi.nlm.nih.gov/pubmed/35145075 http://dx.doi.org/10.1038/s41467-022-28391-9 |
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author | Helf, Maximilian J. Fox, Bennett W. Artyukhin, Alexander B. Zhang, Ying K. Schroeder, Frank C. |
author_facet | Helf, Maximilian J. Fox, Bennett W. Artyukhin, Alexander B. Zhang, Ying K. Schroeder, Frank C. |
author_sort | Helf, Maximilian J. |
collection | PubMed |
description | Untargeted metabolomics via high-resolution mass spectrometry can reveal more than 100,000 molecular features in a single sample, many of which may represent unidentified metabolites, posing significant challenges to data analysis. We here introduce Metaboseek, an open-source analysis platform designed for untargeted comparative metabolomics and demonstrate its utility by uncovering biosynthetic functions of a conserved fat metabolism pathway, α-oxidation, using C. elegans as a model. Metaboseek integrates modules for molecular feature detection, statistics, molecular formula prediction, and fragmentation analysis, which uncovers more than 200 previously uncharacterized α-oxidation-dependent metabolites in an untargeted comparison of wildtype and α-oxidation-defective hacl-1 mutants. The identified metabolites support the predicted enzymatic function of HACL-1 and reveal that α-oxidation participates in metabolism of endogenous β-methyl-branched fatty acids and food-derived cyclopropane lipids. Our results showcase compound discovery and feature annotation at scale via untargeted comparative metabolomics applied to a conserved primary metabolic pathway and suggest a model for the metabolism of cyclopropane lipids. |
format | Online Article Text |
id | pubmed-8831614 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-88316142022-03-04 Comparative metabolomics with Metaboseek reveals functions of a conserved fat metabolism pathway in C. elegans Helf, Maximilian J. Fox, Bennett W. Artyukhin, Alexander B. Zhang, Ying K. Schroeder, Frank C. Nat Commun Article Untargeted metabolomics via high-resolution mass spectrometry can reveal more than 100,000 molecular features in a single sample, many of which may represent unidentified metabolites, posing significant challenges to data analysis. We here introduce Metaboseek, an open-source analysis platform designed for untargeted comparative metabolomics and demonstrate its utility by uncovering biosynthetic functions of a conserved fat metabolism pathway, α-oxidation, using C. elegans as a model. Metaboseek integrates modules for molecular feature detection, statistics, molecular formula prediction, and fragmentation analysis, which uncovers more than 200 previously uncharacterized α-oxidation-dependent metabolites in an untargeted comparison of wildtype and α-oxidation-defective hacl-1 mutants. The identified metabolites support the predicted enzymatic function of HACL-1 and reveal that α-oxidation participates in metabolism of endogenous β-methyl-branched fatty acids and food-derived cyclopropane lipids. Our results showcase compound discovery and feature annotation at scale via untargeted comparative metabolomics applied to a conserved primary metabolic pathway and suggest a model for the metabolism of cyclopropane lipids. Nature Publishing Group UK 2022-02-10 /pmc/articles/PMC8831614/ /pubmed/35145075 http://dx.doi.org/10.1038/s41467-022-28391-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Helf, Maximilian J. Fox, Bennett W. Artyukhin, Alexander B. Zhang, Ying K. Schroeder, Frank C. Comparative metabolomics with Metaboseek reveals functions of a conserved fat metabolism pathway in C. elegans |
title | Comparative metabolomics with Metaboseek reveals functions of a conserved fat metabolism pathway in C. elegans |
title_full | Comparative metabolomics with Metaboseek reveals functions of a conserved fat metabolism pathway in C. elegans |
title_fullStr | Comparative metabolomics with Metaboseek reveals functions of a conserved fat metabolism pathway in C. elegans |
title_full_unstemmed | Comparative metabolomics with Metaboseek reveals functions of a conserved fat metabolism pathway in C. elegans |
title_short | Comparative metabolomics with Metaboseek reveals functions of a conserved fat metabolism pathway in C. elegans |
title_sort | comparative metabolomics with metaboseek reveals functions of a conserved fat metabolism pathway in c. elegans |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8831614/ https://www.ncbi.nlm.nih.gov/pubmed/35145075 http://dx.doi.org/10.1038/s41467-022-28391-9 |
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