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Coenzyme Q10 trapping in mitochondrial complex I underlies Leber’s hereditary optic neuropathy
How does a single amino acid mutation occurring in the blinding disease, Leber’s hereditary optic neuropathy (LHON), impair electron shuttling in mitochondria? We investigated changes induced by the m.3460 G>A mutation in mitochondrial protein ND1 using the tools of Molecular Dynamics and Free En...
Autores principales: | Fuller, Jack T., Barnes, Steven, Sadun, Lorenzo A., Ajmera, Pujan, Alexandrova, Anastassia N., Sadun, Alfredo A. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10523484/ https://www.ncbi.nlm.nih.gov/pubmed/37733737 http://dx.doi.org/10.1073/pnas.2304884120 |
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