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Computational Design of a PDZ Domain Peptide Inhibitor that Rescues CFTR Activity
The cystic fibrosis transmembrane conductance regulator (CFTR) is an epithelial chloride channel mutated in patients with cystic fibrosis (CF). The most prevalent CFTR mutation, ΔF508, blocks folding in the endoplasmic reticulum. Recent work has shown that some ΔF508-CFTR channel activity can be rec...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Public Library of Science
2012
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3330111/ https://ncbi.nlm.nih.gov/pubmed/22532795 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pcbi.1002477 |
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