Literature DB >> 30608643

Extending the Scope of 1H NMR Spectroscopy for the Analysis of Cellular Coenzyme A and Acetyl Coenzyme A.

G A Nagana Gowda, Lauren Abell, Rong Tian.   

Abstract

Coenzyme A (CoA) and acetyl-coenzyme A (acetyl-CoA) are ubiquitous cellular molecules, which mediate hundreds of anabolic and catabolic reactions including energy metabolism. Highly sensitive methods including absorption spectroscopy and mass spectrometry enable their analysis, albeit with many limitations. To date, however, NMR spectroscopy has not been used to analyze these important molecules. Building on our recent efforts, which enabled simultaneous analysis of a large number of metabolites in tissue and blood including many coenzymes and antioxidants ( Anal. Chem. 2016, 88, 4817-24; ibid 2017, 89, 4620-4627), we describe here a new method for identification and quantitation of CoA and acetyl-CoA ex vivo in tissue. Using mouse heart, kidney, liver, brain, and skeletal tissue, we show that a simple 1H NMR experiment can simultaneously measure these molecules. Identification of the two species involved a comprehensive analysis of the different tissue types using 1D and 2D NMR, in combination with spectral databases for standards, as well as spiking with authentic compounds. Time dependent studies showed that while the acetyl-CoA levels remain unaltered, CoA levels diminish by more than 50% within 24 h, which indicates that CoA is labile in solution; however, degassing the sample with helium gas halted its oxidation. Further, interestingly, we also identified endogenous coenzyme A glutathione disulfide (CoA-S-S-G) in tissue for the first time by NMR and show that CoA, when oxidized in tissue extract, also forms the same disulfide metabolite. The ability to simultaneously visualize absolute concentrations of CoA, acetyl-CoA, and endogenous CoA-S-S-G along with redox coenzymes (NAD+, NADH, NADP+, NADPH), energy coenzymes (ATP, ADP, AMP), antioxidants (GSH, GSSG), and a vast pool of other metabolites using a single 1D NMR spectrum offers a new avenue in the metabolomics field for investigation of cellular function in health and disease.

Entities:  

Year:  2019        PMID: 30608643      PMCID: PMC6810604          DOI: 10.1021/acs.analchem.8b05286

Source DB:  PubMed          Journal:  Anal Chem        ISSN: 0003-2700            Impact factor:   6.986


  46 in total

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Journal:  Anal Biochem       Date:  1981-11-15       Impact factor: 3.365

5.  Malonyl-CoA: acetyl-CoA cycling. A new micromethod for determination of acyl-CoAs with malonate decarboxylase.

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Review 6.  Role of CoA and acetyl-CoA in regulating cardiac fatty acid and glucose oxidation.

Authors:  Osama Abo Alrob; Gary D Lopaschuk
Journal:  Biochem Soc Trans       Date:  2014-08       Impact factor: 5.407

7.  Assessment of cardiac function and energetics in isolated mouse hearts using 31P NMR spectroscopy.

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Review 8.  Acetyl-CoA and the regulation of metabolism: mechanisms and consequences.

Authors:  Lei Shi; Benjamin P Tu
Journal:  Curr Opin Cell Biol       Date:  2015-02-20       Impact factor: 8.382

9.  BioMagResBank.

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Journal:  Nucleic Acids Res       Date:  2007-11-04       Impact factor: 16.971

10.  Expanding the limits of human blood metabolite quantitation using NMR spectroscopy.

Authors:  G A Nagana Gowda; Yashas N Gowda; Daniel Raftery
Journal:  Anal Chem       Date:  2014-12-08       Impact factor: 6.986

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  4 in total

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Journal:  Methods Mol Biol       Date:  2019

2.  NMR as a readout to monitor and restore the integrity of complex chemoenzymatic reactions.

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3.  NMR-Based Metabolomics.

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Journal:  Adv Exp Med Biol       Date:  2021       Impact factor: 2.622

Review 4.  Mitochondrial electron transport chain: Oxidative phosphorylation, oxidant production, and methods of measurement.

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Journal:  Redox Biol       Date:  2020-08-06       Impact factor: 11.799

  4 in total

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