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Ergothioneine boosts mitochondrial respiration and exercise performance via direct activation of MPST.

Hans-Georg SprengerMelanie J MittenbühlerYizhi SunJonathan G Van VrankenSebastian SchindlerAbhilash JayarajSumeet A KhetarpalAriana Vargas-CastilloAnna M PuszynskaJessica B SpinelliAndrea ArmaniTenzin KunchokBirgitta RybackHyuk-Soo SeoKijun SongLuke SebastianCoby O'YoungChelsea BraithwaiteSirano Dhe-PaganonNils BurgerEvanna L MillsSteven P GygiHaribabu ArthanariEdward T ChouchaniDavid M SabatiniBruce M Spiegelman
Published in: bioRxiv : the preprint server for biology (2024)
Ergothioneine (EGT) is a diet-derived, atypical amino acid that accumulates to high levels in human tissues. Reduced EGT levels have been linked to age-related disorders, including neurodegenerative and cardiovascular diseases, while EGT supplementation is protective in a broad range of disease and aging models in mice. Despite these promising data, the direct and physiologically relevant molecular target of EGT has remained elusive. Here we use a systematic approach to identify how mitochondria remodel their metabolome in response to exercise training. From this data, we find that EGT accumulates in muscle mitochondria upon exercise training. Proteome-wide thermal stability studies identify 3-mercaptopyruvate sulfurtransferase (MPST) as a direct molecular target of EGT; EGT binds to and activates MPST, thereby boosting mitochondrial respiration and exercise training performance in mice. Together, these data identify the first physiologically relevant EGT target and establish the EGT-MPST axis as a molecular mechanism for regulating mitochondrial function and exercise performance.
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