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The Relative Binding Affinities of PDZ Partners for CFTR: A Biochemical Basis for Efficient Endocytic Recycling

The cystic fibrosis transmembrane conductance regulator (CFTR) is an epithelial chloride channel mutated in patients with cystic fibrosis. Its expression and functional interactions in the apical membrane are regulated by several PDZ (PSD-95, discs large, zonula occludens-1) proteins, which mediate...

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Détails bibliographiques
Auteurs principaux: Cushing, Patrick R., Fellows, Abigail, Villone, Daniel, Boisguerin, Prisca, Madden, Dean R.
Format: Artigo
Langue:Inglês
Publié: 2008
Sujets:
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC2582146/
https://ncbi.nlm.nih.gov/pubmed/18754678
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/bi8003928
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