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Nonequilibrium gating of CFTR on an equilibrium theme.


ABSTRACT: 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. Potential clinical relevance and implications to ABC transporter function are also discussed.

SUBMITTER: Jih KY 

PROVIDER: S-EPMC4931552 | biostudies-literature | 2012 Dec

REPOSITORIES: biostudies-literature

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Nonequilibrium gating of CFTR on an equilibrium theme.

Jih Kang-Yang KY   Hwang Tzyh-Chang TC  

Physiology (Bethesda, Md.) 20121201 6


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. Potential clinical relevance and implications to ABC transporter function are also discussed. ...[more]

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