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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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Veröffentlicht in:Proc Natl Acad Sci U S A
Hauptverfasser: Yu, Yong, Shi, Lei, Karlin, Arthur
Format: Artigo
Sprache:Inglês
Veröffentlicht: National Academy of Sciences 2003
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Online-Zugang: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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