Associated Papers
Trikafta restores thermodynamic coupling between two nucleotide binding domains for potentiating CFTR activity.
Wang G
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie, 2026
Thermodynamic Coupling between Folding Correctors and the First of Dimerized Nucleotide Binding Domains in CFTR.
Wang G
Acs Bio & Med Chem Au, 2025
Thermodynamic coupling between folding correctors and the first of dimerized nucleotide binding domains in CFTR.
Wang G
Research Square, 2025
Effects of Point Mutations on the Thermal Stability of the NBD1 Domain of hCFTR.
Lublin L et al.
Journal of Chemical Information and Modeling, 2025
Allosteric inhibition of CFTR gating by CFTRinh-172 binding in the pore.
Gao X et al.
Nature Communications, 2024
Folding correctors can restore CFTR posttranslational folding landscape by allosteric domain-domain coupling.
Soya N et al.
Nature Communications, 2023
Folding correctors can restore CFTR posttranslational folding landscape by allosteric domain-domain coupling.
Soya N et al.
Biorxiv : the Preprint Server for Biology, 2023
A small molecule high throughput screening platform to profile conformational properties of nascent, ribosome-bound proteins.
Shishido H et al.
Scientific Reports, 2022
A topological switch in CFTR modulates channel activity and sensitivity to unfolding.
Scholl D et al.
Nature Chemical Biology, 2021
Stability Prediction for Mutations in the Cytosolic Domains of Cystic Fibrosis Transmembrane Conductance Regulator.
Bahia MS et al.
Journal of Chemical Information and Modeling, 2021
CFTR trafficking mutations disrupt cotranslational protein folding by targeting biosynthetic intermediates.
Shishido H et al.
Nature Communications, 2020
Disease-relevant mutations alter amino acid co-evolution networks in the second nucleotide binding domain of CFTR.
Ivey G et al.
Plos One, 2020
Differential thermostability and response to cystic fibrosis transmembrane conductance regulator potentiators of human and mouse F508del-CFTR.
Bose SJ et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology, 2019
Domain-interface dynamics of CFTR revealed by stabilizing nanobodies.
Sigoillot M et al.
Nature Communications, 2019
Cryo-EM Visualization of an Active High Open Probability CFTR Anion Channel.
Fay JF et al.
Biochemistry, 2018
Structural stability of purified human CFTR is systematically improved by mutations in nucleotide binding domain 1.
Yang Z et al.
Biochimica Et Biophysica Acta. Biomembranes, 2018
Substitution of Yor1p NBD1 residues improves the thermal stability of Human Cystic Fibrosis Transmembrane Conductance Regulator.
Xavier BM et al.
Protein Engineering, Design & Selection : Peds, 2017
Stabilization of a nucleotide-binding domain of the cystic fibrosis transmembrane conductance regulator yields insight into disease-causing mutations.
Vernon RM et al.
The Journal of Biological Chemistry, 2017
Specific stabilization of CFTR by phosphatidylserine.
Hildebrandt E et al.
Biochimica Et Biophysica Acta. Biomembranes, 2017
Thermal unfolding simulations of NBD1 domain variants reveal structural motifs associated with the impaired folding of F508del-CFTR.
Estácio SG et al.
Molecular Biosystems, 2016
Thermal stability of purified and reconstituted CFTR in a locked open channel conformation.
Aleksandrov LA et al.
Protein Expression and Purification, 2015
Exploiting species differences to understand the CFTR Cl- channel.
Bose SJ et al.
Biochemical Society Transactions, 2015
Deletion of Phenylalanine 508 in the First Nucleotide-binding Domain of the Cystic Fibrosis Transmembrane Conductance Regulator Increases Conformational Exchange and Inhibits Dimerization.
Chong PA et al.
The Journal of Biological Chemistry, 2015
Impact of the F508del mutation on ovine CFTR, a Cl- channel with enhanced conductance and ATP-dependent gating.
Cai Z et al.
The Journal of Physiology, 2015
Rational Coupled Dynamics Network Manipulation Rescues Disease-Relevant Mutant Cystic Fibrosis Transmembrane Conductance Regulator.
Proctor EA et al.
Chemical Science, 2015
Restoration of NBD1 thermal stability is necessary and sufficient to correct ∆F508 CFTR folding and assembly.
He L et al.
Journal of Molecular Biology, 2015
Revertant mutants modify, but do not rescue, the gating defect of the cystic fibrosis mutant G551D-CFTR.
Xu Z et al.
The Journal of Physiology, 2014
Correctors of ΔF508 CFTR restore global conformational maturation without thermally stabilizing the mutant protein.
He L et al.
Faseb Journal : Official Publication of the Federation of American Societies for Experimental Biology, 2013
Allosteric modulation balances thermodynamic stability and restores function of ΔF508 CFTR.
Aleksandrov AA et al.
Journal of Molecular Biology, 2012