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Mutant huntingtin disrupts mitochondrial proteostasis by interacting with TIM23
Mutant huntingtin (mHTT), the causative protein in Huntington’s disease (HD), associates with the translocase of mitochondrial inner membrane 23 (TIM23) complex, resulting in inhibition of synaptic mitochondrial protein import first detected in presymptomatic HD mice. The early timing of this event...
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| Udgivet i: | Proc Natl Acad Sci U S A |
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| Main Authors: | , , , , , , , , , , , , , , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
National Academy of Sciences
2019
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6697818/ https://ncbi.nlm.nih.gov/pubmed/31346086 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.1904101116 |
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