New insights into structure and function of bis-phosphinic acid derivatives and implications for CFTR modulation
暂无分享,去创建一个
J. Mornon | I. Sermet-Gaudelus | I. Callebaut | N. Servel | A. Edelman | S. Bitam | C. Gravier-Pelletier | A. Hinzpeter | B. Hoffmann | A. Elbahnsi | I. Pranke | D. Tondelier | G. Prestat | A. Hatton | A. Lepissier | Alexandra Pastor | Geordie Creste | F. Berhal | B. Chevalier | Mélanie Faria da Cunha | Christelle Moquereau | Nesrine Baatalah
[1] L. Lands,et al. Elexacaftor-Tezacaftor-Ivacaftor for Cystic Fibrosis with a Single Phe508del Allele. , 2019, The New England journal of medicine.
[2] Jue Chen,et al. Molecular structure of the ATP-bound, phosphorylated human CFTR , 2018, Proceedings of the National Academy of Sciences.
[3] F. van Goor,et al. VX‐445–Tezacaftor–Ivacaftor in Patients with Cystic Fibrosis and One or Two Phe508del Alleles , 2018, The New England journal of medicine.
[4] A. Orth,et al. Structure-guided combination therapy to potently improve the function of mutant CFTRs , 2018, Nature Medicine.
[5] C. Bear,et al. Correctors of the Major Cystic Fibrosis Mutant Interact through Membrane-Spanning Domains , 2018, Molecular Pharmacology.
[6] J. Mornon,et al. Combining theoretical and experimental data to decipher CFTR 3D structures and functions , 2018, Cellular and Molecular Life Sciences.
[7] M. Baaden,et al. Holding the Nucleosome Together: A Quantitative Description of the DNA-Histone Interface in Solution. , 2018, Journal of chemical theory and computation.
[8] J. Jais,et al. Correction of CFTR function in nasal epithelial cells from cystic fibrosis patients predicts improvement of respiratory function by CFTR modulators , 2017, Scientific Reports.
[9] Zhengrong Yang,et al. Direct Binding of the Corrector VX-809 to Human CFTR NBD1: Evidence of an Allosteric Coupling between the Binding Site and the NBD1:CL4 Interface , 2017, Molecular Pharmacology.
[10] P. Palange,et al. Cystic fibrosis , 2016, The Lancet.
[11] Garry R. Cutting,et al. From CFTR biology toward combinatorial pharmacotherapy: expanded classification of cystic fibrosis mutations , 2016, Molecular biology of the cell.
[12] J. Forman-Kay,et al. Binding screen for cystic fibrosis transmembrane conductance regulator correctors finds new chemical matter and yields insights into cystic fibrosis therapeutic strategy , 2016, Protein science : a publication of the Protein Society.
[13] Alexander D. MacKerell,et al. CHARMM-GUI Input Generator for NAMD, GROMACS, AMBER, OpenMM, and CHARMM/OpenMM Simulations Using the CHARMM36 Additive Force Field , 2015, Journal of chemical theory and computation.
[14] I. Sermet-Gaudelus,et al. An unexpected effect of TNF-α on F508del-CFTR maturation and function , 2015, F1000Research.
[15] B. Joris,et al. 5'-Methylene-triazole-substituted-aminoribosyl uridines as MraY inhibitors: synthesis, biological evaluation and molecular modeling. , 2015, Organic & biomolecular chemistry.
[16] S. Jonić,et al. Full-open and closed CFTR channels, with lateral tunnels from the cytoplasm and an alternative position of the F508 region, as revealed by molecular dynamics , 2015, Cellular and Molecular Life Sciences.
[17] Zhengrong Yang,et al. Restoration of NBD1 thermal stability is necessary and sufficient to correct ∆F508 CFTR folding and assembly. , 2015, Journal of molecular biology.
[18] Sunhwan Jo,et al. CHARMM‐GUI Membrane Builder toward realistic biological membrane simulations , 2014, J. Comput. Chem..
[19] I. Sermet-Gaudelus,et al. Biosynthesis of cystic fibrosis transmembrane conductance regulator. , 2014, The international journal of biochemistry & cell biology.
[20] Hong Yu Ren,et al. VX-809 corrects folding defects in cystic fibrosis transmembrane conductance regulator protein through action on membrane-spanning domain 1 , 2013, Molecular biology of the cell.
[21] Piotr Zielenkiewicz,et al. Discovery of novel potent ΔF508-CFTR correctors that target the nucleotide binding domain , 2013, EMBO molecular medicine.
[22] Marisa Sousa,et al. Revertants, low temperature, and correctors reveal the mechanism of F508del-CFTR rescue by VX-809 and suggest multiple agents for full correction. , 2013, Chemistry & biology.
[23] G. Lukács,et al. Mechanism-based corrector combination restores ΔF508-CFTR folding and function , 2013, Nature Chemical Biology.
[24] J. Riordan,et al. Correctors of ΔF508 CFTR restore global conformational maturation without thermally stabilizing the mutant protein , 2013, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
[25] Holger Gohlke,et al. MMPBSA.py: An Efficient Program for End-State Free Energy Calculations. , 2012, Journal of chemical theory and computation.
[26] Pradeep Kota,et al. Allosteric modulation balances thermodynamic stability and restores function of ΔF508 CFTR. , 2012, Journal of molecular biology.
[27] A S Verkman,et al. CFTR: folding, misfolding and correcting the ΔF508 conformational defect. , 2012, Trends in molecular medicine.
[28] K. Du,et al. Correction of Both NBD1 Energetics and Domain Interface Is Required to Restore ΔF508 CFTR Folding and Function , 2012, Cell.
[29] Philip J. Thomas,et al. Requirements for Efficient Correction of ΔF508 CFTR Revealed by Analyses of Evolved Sequences , 2012, Cell.
[30] Alexander D. MacKerell,et al. Optimization of the CHARMM additive force field for DNA: Improved treatment of the BI/BII conformational equilibrium. , 2012, Journal of chemical theory and computation.
[31] Matthias Griese,et al. A CFTR potentiator in patients with cystic fibrosis and the G551D mutation. , 2011, The New England journal of medicine.
[32] P. Negulescu,et al. Correction of the F508del-CFTR protein processing defect in vitro by the investigational drug VX-809 , 2011, Proceedings of the National Academy of Sciences.
[33] Alexandre G. de Brevern,et al. Comparative Analysis of Threshold and Tessellation Methods for Determining Protein Contacts , 2011, J. Chem. Inf. Model..
[34] Zhengrong Yang,et al. Thermal unfolding studies show the disease causing F508del mutation in CFTR thermodynamically destabilizes nucleotide‐binding domain 1 , 2010, Protein science : a publication of the Protein Society.
[35] H. Senderowitz,et al. The Cystic Fibrosis-causing Mutation ΔF508 Affects Multiple Steps in Cystic Fibrosis Transmembrane Conductance Regulator Biogenesis* , 2010, The Journal of Biological Chemistry.
[36] Alexander D. MacKerell,et al. Update of the CHARMM all-atom additive force field for lipids: validation on six lipid types. , 2010, The journal of physical chemistry. B.
[37] Alexandre G. de Brevern,et al. A Novel Evaluation of Residue and Protein Volumes by Means of Laguerre Tessellation , 2010, J. Chem. Inf. Model..
[38] S. Freedman,et al. Cystic fibrosis , 2009, The Lancet.
[39] Taehoon Kim,et al. CHARMM‐GUI: A web‐based graphical user interface for CHARMM , 2008, J. Comput. Chem..
[40] P. Zielenkiewicz,et al. DeltaF508 mutation increases conformational flexibility of CFTR protein. , 2008, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.
[41] M. Amaral,et al. Solubilizing mutations used to crystallize one CFTR domain attenuate the trafficking and channel defects caused by the major cystic fibrosis mutation. , 2008, Chemistry & biology.
[42] Paola Vergani,et al. The ABC protein turned chloride channel whose failure causes cystic fibrosis , 2006, Nature.
[43] J. M. Sauder,et al. Impact of the ΔF508 Mutation in First Nucleotide-binding Domain of Human Cystic Fibrosis Transmembrane Conductance Regulator on Domain Folding and Structure* , 2005, Journal of Biological Chemistry.
[44] Matthew P. Repasky,et al. Glide: a new approach for rapid, accurate docking and scoring. 1. Method and assessment of docking accuracy. , 2004, Journal of medicinal chemistry.
[45] K Schulten,et al. VMD: visual molecular dynamics. , 1996, Journal of molecular graphics.
[46] L. Tsui,et al. Erratum: Identification of the Cystic Fibrosis Gene: Cloning and Characterization of Complementary DNA , 1989, Science.
[47] N. Guex,et al. SWISS‐MODEL and the Swiss‐Pdb Viewer: An environment for comparative protein modeling , 1997, Electrophoresis.
[48] L. Tsui,et al. Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA. , 1989, Science.
[49] J. Gustafson,et al. Cystic Fibrosis , 2009, Journal of the Iowa Medical Society.