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Hyperpolarized NMR Metabolomics at Natural (13)C Abundance

[Image: see text] Metabolomics plays a pivotal role in systems biology, and NMR is a central tool with high precision and exceptional resolution of chemical information. Most NMR metabolomic studies are based on (1)H 1D spectroscopy, severely limited by peak overlap. (13)C NMR benefits from a larger...

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Autores principales: Dey, Arnab, Charrier, Benoît, Martineau, Estelle, Deborde, Catherine, Gandriau, Elodie, Moing, Annick, Jacob, Daniel, Eshchenko, Dmitry, Schnell, Marc, Melzi, Roberto, Kurzbach, Dennis, Ceillier, Morgan, Chappuis, Quentin, Cousin, Samuel F., Kempf, James G., Jannin, Sami, Dumez, Jean-Nicolas, Giraudeau, Patrick
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2020
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7705890/
https://www.ncbi.nlm.nih.gov/pubmed/33136383
http://dx.doi.org/10.1021/acs.analchem.0c03510
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author Dey, Arnab
Charrier, Benoît
Martineau, Estelle
Deborde, Catherine
Gandriau, Elodie
Moing, Annick
Jacob, Daniel
Eshchenko, Dmitry
Schnell, Marc
Melzi, Roberto
Kurzbach, Dennis
Ceillier, Morgan
Chappuis, Quentin
Cousin, Samuel F.
Kempf, James G.
Jannin, Sami
Dumez, Jean-Nicolas
Giraudeau, Patrick
author_facet Dey, Arnab
Charrier, Benoît
Martineau, Estelle
Deborde, Catherine
Gandriau, Elodie
Moing, Annick
Jacob, Daniel
Eshchenko, Dmitry
Schnell, Marc
Melzi, Roberto
Kurzbach, Dennis
Ceillier, Morgan
Chappuis, Quentin
Cousin, Samuel F.
Kempf, James G.
Jannin, Sami
Dumez, Jean-Nicolas
Giraudeau, Patrick
author_sort Dey, Arnab
collection PubMed
description [Image: see text] Metabolomics plays a pivotal role in systems biology, and NMR is a central tool with high precision and exceptional resolution of chemical information. Most NMR metabolomic studies are based on (1)H 1D spectroscopy, severely limited by peak overlap. (13)C NMR benefits from a larger signal dispersion but is barely used in metabolomics due to ca. 6000-fold lower sensitivity. We introduce a new approach, based on hyperpolarized (13)C NMR at natural abundance, that circumvents this limitation. A new untargeted NMR-based metabolomic workflow based on dissolution dynamic nuclear polarization (d-DNP) for the first time enabled hyperpolarized natural abundance (13)C metabolomics. Statistical analysis of resulting hyperpolarized (13)C data distinguishes two groups of plant (tomato) extracts and highlights biomarkers, in full agreement with previous results on the same biological model. We also optimize parameters of the semiautomated d-DNP system suitable for high-throughput studies.
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spelling pubmed-77058902020-12-02 Hyperpolarized NMR Metabolomics at Natural (13)C Abundance Dey, Arnab Charrier, Benoît Martineau, Estelle Deborde, Catherine Gandriau, Elodie Moing, Annick Jacob, Daniel Eshchenko, Dmitry Schnell, Marc Melzi, Roberto Kurzbach, Dennis Ceillier, Morgan Chappuis, Quentin Cousin, Samuel F. Kempf, James G. Jannin, Sami Dumez, Jean-Nicolas Giraudeau, Patrick Anal Chem [Image: see text] Metabolomics plays a pivotal role in systems biology, and NMR is a central tool with high precision and exceptional resolution of chemical information. Most NMR metabolomic studies are based on (1)H 1D spectroscopy, severely limited by peak overlap. (13)C NMR benefits from a larger signal dispersion but is barely used in metabolomics due to ca. 6000-fold lower sensitivity. We introduce a new approach, based on hyperpolarized (13)C NMR at natural abundance, that circumvents this limitation. A new untargeted NMR-based metabolomic workflow based on dissolution dynamic nuclear polarization (d-DNP) for the first time enabled hyperpolarized natural abundance (13)C metabolomics. Statistical analysis of resulting hyperpolarized (13)C data distinguishes two groups of plant (tomato) extracts and highlights biomarkers, in full agreement with previous results on the same biological model. We also optimize parameters of the semiautomated d-DNP system suitable for high-throughput studies. American Chemical Society 2020-11-02 2020-11-17 /pmc/articles/PMC7705890/ /pubmed/33136383 http://dx.doi.org/10.1021/acs.analchem.0c03510 Text en © 2020 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Dey, Arnab
Charrier, Benoît
Martineau, Estelle
Deborde, Catherine
Gandriau, Elodie
Moing, Annick
Jacob, Daniel
Eshchenko, Dmitry
Schnell, Marc
Melzi, Roberto
Kurzbach, Dennis
Ceillier, Morgan
Chappuis, Quentin
Cousin, Samuel F.
Kempf, James G.
Jannin, Sami
Dumez, Jean-Nicolas
Giraudeau, Patrick
Hyperpolarized NMR Metabolomics at Natural (13)C Abundance
title Hyperpolarized NMR Metabolomics at Natural (13)C Abundance
title_full Hyperpolarized NMR Metabolomics at Natural (13)C Abundance
title_fullStr Hyperpolarized NMR Metabolomics at Natural (13)C Abundance
title_full_unstemmed Hyperpolarized NMR Metabolomics at Natural (13)C Abundance
title_short Hyperpolarized NMR Metabolomics at Natural (13)C Abundance
title_sort hyperpolarized nmr metabolomics at natural (13)c abundance
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7705890/
https://www.ncbi.nlm.nih.gov/pubmed/33136383
http://dx.doi.org/10.1021/acs.analchem.0c03510
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