Hyperpolarized Micro-NMR Platform for Sensitive Analysis of In Vitro Metabolic Flux in Living Cells.
Hyperpolarization
Metabolic flux
Micro-coil
Microfluidics
NMR
Journal
Methods in molecular biology (Clifton, N.J.)
ISSN: 1940-6029
Titre abrégé: Methods Mol Biol
Pays: United States
ID NLM: 9214969
Informations de publication
Date de publication:
2022
2022
Historique:
entrez:
27
11
2021
pubmed:
28
11
2021
medline:
21
1
2022
Statut:
ppublish
Résumé
Metabolism represents an ensemble of cellular biochemical reactions, and thus metabolic analyses can shed light on the state of cells. Metabolic changes in response to external cues, such as drug treatment, for example, can be rapid and potentially an early indicator of therapeutic response. Unfortunately, conventional techniques to study metabolism, such as optical microscopy or mass spectrometry, have functional limitations in specificity and sensitivity. To address this technical need, we developed a sensitive analytical tool based on nuclear magnetic resonance (NMR) technology, termed hyperpolarized micro-NMR, that enables rapid quantification of multiple metabolic fluxes in a small number of cells, down to 10,000 cells, nondestructively. This analytical capability was achieved by miniaturization of an NMR detection coil along with hyperpolarization of endogenous metabolites. Using this tool, we were able to quantify pyruvate-to-lactate flux in cancer stem cells nondestructively within 2 min, which has not been possible with other techniques. With further optimization, we envision that this novel device could be a powerful analytical platform for sensitive analysis of metabolism in mass-limited samples.
Identifiants
pubmed: 34837199
doi: 10.1007/978-1-0716-1803-5_29
pmc: PMC9541228
mid: NIHMS1837928
doi:
Substances chimiques
Carbon Isotopes
0
Pyruvic Acid
8558G7RUTR
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
561-569Subventions
Organisme : NCI NIH HHS
ID : K99 CA226357
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States
Organisme : NIBIB NIH HHS
ID : R00 EB014328
Pays : United States
Organisme : NCI NIH HHS
ID : R21 CA212958
Pays : United States
Informations de copyright
© 2022. Springer Science+Business Media, LLC, part of Springer Nature.
Références
Cell Metab. 2016 Jan 12;23(1):27-47
pubmed: 26771115
Nat Cell Biol. 2017 Nov;19(11):1298-1306
pubmed: 29058720
Chem Soc Rev. 2014 Mar 7;43(5):1627-59
pubmed: 24363044
Science. 2009 May 22;324(5930):1029-33
pubmed: 19460998
ACS Chem Biol. 2019 Apr 19;14(4):665-673
pubmed: 30893552
Proc Natl Acad Sci U S A. 2003 Sep 2;100(18):10158-63
pubmed: 12930897
Cancer Res. 2018 Jul 15;78(14):3755-3760
pubmed: 29769199
Sci Rep. 2016 Sep 06;6:32846
pubmed: 27597137
Sci Adv. 2016 May 27;2(5):e1600200
pubmed: 27386546
Cell Metab. 2017 Dec 5;26(6):830-841.e3
pubmed: 29056515
Cell. 2015 Sep 10;162(6):1229-41
pubmed: 26321679
J Magn Reson. 2018 Oct;295:57-62
pubmed: 30099234
Sci Adv. 2017 Jun 16;3(6):e1700341
pubmed: 28630930
Magn Reson Med. 2019 Mar;81(3):2184-2194
pubmed: 30357898
Cancer Res. 2019 Jan 1;79(1):242-250
pubmed: 30459151
Cancer Res. 2017 Jun 1;77(11):3113-3120
pubmed: 28386017
Cell Metab. 2020 Jan 7;31(1):105-114.e3
pubmed: 31564440