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Structural effects of quinacrine binding in the open channel of the acetylcholine receptor

Noncompetitive inhibitors of the nicotinic acetylcholine (ACh) receptors suppress cation flux directly by binding in and blocking the open channel or indirectly by stabilizing closed states of the receptor. The lidocaine derivative QX-314 and the acridine derivative quinacrine act directly as open c...

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Detalles Bibliográficos
Publicado en:Proc Natl Acad Sci U S A
Autores principales: Yu, Yong, Shi, Lei, Karlin, Arthur
Formato: Artigo
Lenguaje:Inglês
Publicado: National Academy of Sciences 2003
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Acceso en línea:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC153021/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/12644710/
https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.0730718100
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