Spontaneous hydrolysis and spurious metabolic properties of α-ketoglutarate esters

Nat Commun. 2021 Aug 12;12(1):4905. doi: 10.1038/s41467-021-25228-9.

Abstract

α-ketoglutarate (KG), also referred to as 2-oxoglutarate, is a key intermediate of cellular metabolism with pleiotropic functions. Cell-permeable esterified analogs are widely used to study how KG fuels bioenergetic and amino acid metabolism and DNA, RNA, and protein hydroxylation reactions, as cellular membranes are thought to be impermeable to KG. Here we show that esterified KG analogs rapidly hydrolyze in aqueous media, yielding KG that, in contrast to prevailing assumptions, imports into many cell lines. Esterified KG analogs exhibit spurious KG-independent effects on cellular metabolism, including extracellular acidification, arising from rapid hydrolysis and de-protonation of α-ketoesters, and significant analog-specific inhibitory effects on glycolysis or mitochondrial respiration. We observe that imported KG decarboxylates to succinate in the cytosol and contributes minimally to mitochondrial metabolism in many cell lines cultured in normal conditions. These findings demonstrate that nuclear and cytosolic KG-dependent reactions may derive KG from functionally distinct subcellular pools and sources.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acids / metabolism*
  • Animals
  • Cell Line, Tumor
  • Cytosol / metabolism
  • Energy Metabolism*
  • Esters / chemistry
  • Esters / metabolism*
  • Glycolysis
  • HEK293 Cells
  • Humans
  • Hydrolysis
  • Hydrophobic and Hydrophilic Interactions
  • Ketoglutaric Acids / chemistry
  • Ketoglutaric Acids / metabolism*
  • Mice
  • Mitochondria / metabolism*
  • Oxygen Consumption
  • RAW 264.7 Cells
  • Succinic Acid / metabolism*

Substances

  • Amino Acids
  • Esters
  • Ketoglutaric Acids
  • Succinic Acid