The mitochondrial F 1 F o ‐ATP synthase uses a rotary mechanism to synthesise ATP. This mechanism can, however, also operate in reverse, pumping protons at the expense of ATP, with significant potential implications for mitochondrial and age‐related diseases. In a recent study, Acin‐Perez et al (2023) use an elegant assay to screen compounds for the capacity to selectively inhibit ATP hydrolysis without affecting ATP synthesis. They show that (+)‐epicatechin is one such compound and has significant benefits for cell and tissue function in disease models. These findings signpost a novel therapeutic approach for mitochondrial disease.
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CITATION STYLE
Valdebenito, G. E., Chacko, A. R., & Duchen, M. R. (2023). The mitochondrial ATP synthase as an ATP consumer—a surprising therapeutic target. The EMBO Journal, 42(10). https://doi.org/10.15252/embj.2023114141