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Murphy 2022 Nat Chem Biol

From Bioblast
Publications in the MiPMap
Murphy MP, Chouchani ET (2022) Why succinate? Physiological regulation by a mitochondrial coenzyme Q sentinel. Nat Chem Biol 18:461-9. https://doi.org/10.1038/s41589-022-01004-8

Β» PMID: 35484255 Open Access

Murphy MP, Chouchani ET (2022) Nat Chem Biol

Abstract: Metabolites once considered solely in catabolism or anabolism turn out to have key regulatory functions. Among these, the citric acid cycle intermediate succinate stands out owing to its multiple roles in disparate pathways, its dramatic concentration changes and its selective cell release. Here we propose that succinate has evolved as a signaling modality because its concentration reflects the coenzyme Q (CoQ) pool redox state, a central redox couple confined to the mitochondrial inner membrane. This connection is of general importance because CoQ redox state integrates three bioenergetic parameters: mitochondrial electron supply, oxygen tension and ATP demand. Succinate, by equilibrating with the CoQ pool, enables the status of this central bioenergetic parameter to be communicated from mitochondria to the rest of the cell, into the circulation and to other cells. The logic of this form of regulation explains many emerging roles of succinate in biology, and suggests future research questions.

β€’ Bioblast editor: Gnaiger E


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Enzyme: Complex II;succinate dehydrogenase