Proteomics

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Mitochondrial Protein Hyperacetylation in the Failing Heart

ABSTRACT: Mitochondrial proteomics was used to identify energy metabolic derangements that occur during the early stages of heart failure in well-defined mouse models. Levels of β-hydroxybutyrate dehydrogenase 1 (BDH1), a key enzyme in ketone oxidation, was upregulated. 13C-substrate flux studies and metabolomic profiling confirmed that the hypertrophied and early stage failing heart shifts to ketone bodies as a fuel source in the context of reduced oxidation of fatty acids, the chief substrate for the normal heart. This fuel shift is associated with an expansion of the acetyl pool and reduced levels of NAD+ levels resulting in increased mitochondrial protein acetylation. Myocardium of humans with heart failure also exhibited mitochondrial protein hyperacetylation. We propose that a shift to ketones as a fuel source leads to maladaptive bioenergetic consequences during the development of heart failure.

INSTRUMENT(S): LTQ Orbitrap Elite

ORGANISM(S): Mus Musculus (mouse)

TISSUE(S): Heart

SUBMITTER: Ola Martin  

LAB HEAD: Daniel P. Kelly; Joshua J. Coon

PROVIDER: PXD001652 | Pride | 2016-02-26

REPOSITORIES: Pride

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Dataset's files

Source:
Action DRS
2013_08_12_NMR_mix2_acetyl_1.raw Raw
2013_08_12_NMR_mix2_acetyl_1_FTMS_HCD.csv Csv
2013_08_12_NMR_mix2_acetyl_2.raw Raw
2013_08_12_NMR_mix2_acetyl_2_FTMS_HCD.csv Csv
2013_08_12_NMR_mix2_acetyl_3.raw Raw
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Publications

Myocardial fuel and energy metabolic derangements contribute to the pathogenesis of heart failure. Recent evidence implicates posttranslational mechanisms in the energy metabolic disturbances that contribute to the pathogenesis of heart failure. We hypothesized that accumulation of metabolite intermediates of fuel oxidation pathways drives posttranslational modifications of mitochondrial proteins during the development of heart failure. Myocardial acetylproteomics demonstrated extensive mitochon  ...[more]

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