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The mitochondrial ATP synthase as an ATP consumer-a surprising therapeutic target.
Valdebenito, Gabriel E; Chacko, Anitta R; Duchen, Michael R.
Afiliação
  • Valdebenito GE; UCL Consortium for Mitochondrial Research and Department of Cell and Developmental Biology, University College London, London, UK.
  • Chacko AR; UCL Consortium for Mitochondrial Research and Department of Cell and Developmental Biology, University College London, London, UK.
  • Duchen MR; UCL Consortium for Mitochondrial Research and Department of Cell and Developmental Biology, University College London, London, UK.
EMBO J ; 42(10): e114141, 2023 05 15.
Article em En | MEDLINE | ID: mdl-37021792
ABSTRACT
The mitochondrial F1 Fo -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.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Trifosfato de Adenosina / ATPases Mitocondriais Próton-Translocadoras Tipo de estudo: Prognostic_studies Idioma: En Revista: EMBO J Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Trifosfato de Adenosina / ATPases Mitocondriais Próton-Translocadoras Tipo de estudo: Prognostic_studies Idioma: En Revista: EMBO J Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Reino Unido