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Nonequilibrium Gating of CFTR on an Equilibrium Theme

Malfunction of cystic fibrosis transmembrane conductance regulator (CFTR), a member of the ABC protein superfamily that functions as an ATP-gated chloride channel, causes the lethal genetic disease, cystic fibrosis. This review focuses on the most recent findings on the gating mechanism of CFTR. Pot...

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Dettagli Bibliografici
Pubblicato in:Physiology (Bethesda)
Autori principali: Jih, Kang-Yang, Hwang, Tzyh-Chang
Natura: Artigo
Lingua:Inglês
Pubblicazione: 2012
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC4931552/
https://ncbi.nlm.nih.gov/pubmed/23223629
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1152/physiol.00026.2012
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