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CFTR:New insights into structure and function and implications for modulation by small molecules

Authors :
Kleizen, Bertrand
Hunt, John F.
Callebaut, Isabelle
Hwang, Tzyh Chang
Sermet-Gaudelus, Isabelle
Hafkemeyer, Sylvia
Sheppard, David N.
Sub Cellular Protein Chemistry
Cellular Protein Chemistry
HAL-SU, Gestionnaire
Utrecht University [Utrecht]
Columbia University [New York]
Institut de minéralogie, de physique des matériaux et de cosmochimie (IMPMC)
Muséum national d'Histoire naturelle (MNHN)-Institut de recherche pour le développement [IRD] : UR206-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)
University of Missouri Research Reactor [Columbia] (MURR)
University of Missouri [Columbia] (Mizzou)
University of Missouri System-University of Missouri System
Institut Necker Enfants-Malades (INEM - UM 111 (UMR 8253 / U1151))
Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Université Paris Cité (UPCité)
Mukoviszidose Institut
University of Bristol [Bristol]
Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Université de Paris (UP)
Sub Cellular Protein Chemistry
Cellular Protein Chemistry
Source :
Kleizen, B, Hunt, J, Callebaut, I, Hwang, T-C, Sermet-Gaudelus, I, Hafkemeyer, S & Sheppard, D N 2020, ' CFTR : New insights into structure and function and implications for modulation by small molecules ', Journal of Cystic Fibrosis, vol. 19, no. Supplement 1, pp. S19-S24 . https://doi.org/10.1016/j.jcf.2019.10.021, Journal of Cystic Fibrosis, Journal of Cystic Fibrosis, 2020, 19 (S1), pp.S19-S24. ⟨10.1016/j.jcf.2019.10.021⟩, Journal of Cystic Fibrosis, Elsevier, 2020, 19 (S1), pp.S19-S24. ⟨10.1016/j.jcf.2019.10.021⟩, Journal of Cystic Fibrosis, 19(suppl. 1), s19. Elsevier bedrijfsinformatie b.v.
Publication Year :
2020

Abstract

International audience; Structural biology and functional studies are a powerful combination to elucidate fundamental knowledge about the cystic fibrosis transmembrane conductance regulator (CFTR). Here, we discuss the latest findings, including how clinically-approved drugs restore function to mutant CFTR, leading to better clinical outcomes for people with cystic fibrosis (CF). Despite the prospect of regulatory approval of a CFTR-targeting therapy for most CF mutations, strenuous efforts are still needed to fully comprehend CFTR structure-and-function for the development of better drugs to enable people with CF to live full and active lives.

Details

Language :
English
ISSN :
15691993
Database :
OpenAIRE
Journal :
Kleizen, B, Hunt, J, Callebaut, I, Hwang, T-C, Sermet-Gaudelus, I, Hafkemeyer, S & Sheppard, D N 2020, ' CFTR : New insights into structure and function and implications for modulation by small molecules ', Journal of Cystic Fibrosis, vol. 19, no. Supplement 1, pp. S19-S24 . https://doi.org/10.1016/j.jcf.2019.10.021, Journal of Cystic Fibrosis, Journal of Cystic Fibrosis, 2020, 19 (S1), pp.S19-S24. ⟨10.1016/j.jcf.2019.10.021⟩, Journal of Cystic Fibrosis, Elsevier, 2020, 19 (S1), pp.S19-S24. ⟨10.1016/j.jcf.2019.10.021⟩, Journal of Cystic Fibrosis, 19(suppl. 1), s19. Elsevier bedrijfsinformatie b.v.
Accession number :
edsair.doi.dedup.....116512453739f03c45a8cf7ed7562216
Full Text :
https://doi.org/10.1016/j.jcf.2019.10.021