The CFTR P67L variant reveals a key role for N-terminal lasso helices in channel folding, maturation, and pharmacologic rescue

Patients with cystic fibrosis (CF) harboring the P67L variant in the cystic fibrosis transmembrane conductance regulator (CFTR) often exhibit a typical CF phenotype, including severe respiratory compromise. This rare mutation (reported in <300 patients worldwide) responds robustly to CFTR correct...

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Detalles Bibliográficos
Autores principales: Sabusap, Carleen Mae, Joshi, Disha, Simhaev, Luba, Oliver, Kathryn E., Senderowitz, Hanoch, van Willigen, Marcel, Braakman, Ineke, Rab, Andras, Sorscher, Eric J., Hong, Jeong S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Biochemistry and Molecular Biology 2021
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8102917/
https://www.ncbi.nlm.nih.gov/pubmed/33781744
http://dx.doi.org/10.1016/j.jbc.2021.100598

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8102917/
https://www.ncbi.nlm.nih.gov/pubmed/33781744
http://dx.doi.org/10.1016/j.jbc.2021.100598

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