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Conformational Variability in Ground-State CFTR Lipoprotein Particle Cryo-EM Ensembles

International journal of molecular sciences, 2022-08, Vol.23 (16), p.9248

2022

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Multiple Membrane-Cytoplasmic Domain Contacts in the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Mediate Regulation of Channel Gating

The Journal of biological chemistry, 2008-09, Vol.283 (39), p.26383-26390

2008

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Purification and Crystallization of the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR)

The Journal of biological chemistry, 2004-09, Vol.279 (37), p.39051-39057

2004

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Cryo-EM Visualization of an Active High Open Probability CFTR Anion Channel

Biochemistry (Easton), 2018-10, Vol.57 (43), p.6234-6246

2018

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R‑Domain Phosphorylation by Protein Kinase A Stimulates Dissociation of Unhydrolyzed ATP from the First Nucleotide-Binding Site of the Cystic Fibrosis Transmembrane Conductance Regulator

Biochemistry (Easton), 2018-08, Vol.57 (34), p.5073-5075

2018

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The cubicon method for concentrating membrane proteins in the cubic mesophase

Nature protocols, 2017-09, Vol.12 (9), p.1745-1762

2017

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Membrane protein stability can be compromised by detergent interactions with the extramembranous soluble domains

Protein science, 2014-06, Vol.23 (6), p.769-789

2014

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Allosteric Modulation Balances Thermodynamic Stability and Restores Function of ΔF508 CFTR

Journal of molecular biology, 2012-05, Vol.419 (1-2), p.41-60

2012

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Restoration of domain folding and interdomain assembly by second-site suppressors of the ΔF508 mutation in CFTR

The FASEB journal, 2010-08, Vol.24 (8), p.3103-3112

2010

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The cystic fibrosis transmembrane conductance regulator (CFTR): three-dimensional structure and localization of a channel gate

The Journal of biological chemistry, 2011-12, Vol.286 (49), p.42647-42654

2011

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Thermal stability of purified and reconstituted CFTR in a locked open channel conformation

Protein expression and purification, 2015-12, Vol.116, p.159-166

2015

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CFTR (ABCC7) is a hydrolyzable-ligand-gated channel

Pflügers Archiv, 2007-02, Vol.453 (5), p.693-702

2007

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CFTR (ABCC7) is a hydrolyzable-ligand-gated channel

Pflügers Archiv, 2007-02, Vol.453 (5), p.693-702

2007

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Architecture of the cystic fibrosis transmembrane conductance regulator protein and structural changes associated with phosphorylation and nucleotide binding

Journal of structural biology, 2009-09, Vol.167 (3), p.242-251

2009

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Regulatory Insertion Removal Restores Maturation, Stability and Function of ΔF508 CFTR

Journal of molecular biology, 2010-08, Vol.401 (2), p.194-210

2010

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Do main location within the cystic fibrosis transmembrane conductance regulator protein investigated by electron microscopy and gold labelling

Biochimica et biophysica acta. Biomembranes, 2011-01, Vol.1808 (1), p.399-404

2011

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Multiple Membrane-Cytoplasmic Domain Contacts in the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Mediate Regulation of Channel GatingS

The Journal of biological chemistry, 2008-09, Vol.283 (39), p.26383-26390

2008

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Domain location within the cystic fibrosis transmembrane conductance regulator protein investigated by electron microscopy and gold labelling

Biochimica et biophysica acta, 2011-01, Vol.1808 (1), p.399

2011

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Restoration of domain folding and interdomain assembly by second-site suppressors of the DeltaF508 mutation in CFTR

The FASEB journal, 2010-08, Vol.24 (8), p.3103-3112

2010

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Regulatory insertion removal restores maturation, stability and function of DeltaF508 CFTR

Journal of molecular biology, 2010-08, Vol.401 (2), p.194

2010

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The First Nucleotide Binding Domain of Cystic Fibrosis Transmembrane Conductance Regulator Is a Site of Stable Nucleotide Interaction, whereas the Second Is a Site of Rapid Turnover

The Journal of biological chemistry, 2002-05, Vol.277 (18), p.15419-15425

2002

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The role of cystic fibrosis transmembrane conductance regulator phenylalanine 508 side chain in ion channel gating

The Journal of physiology, 2006-04, Vol.572 (2), p.347-358

2006

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Domain Interdependence in the Biosynthetic Assembly of CFTR

Journal of molecular biology, 2007-01, Vol.365 (4), p.981-994

2007

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The non-hydrolytic pathway of cystic fibrosis transmembrane conductance regulator ion channel gating

The Journal of physiology, 2000-10, Vol.528 (2), p.259-265

2000

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Differential Interactions of Nucleotides at the Two Nucleotide Binding Domains of the Cystic Fibrosis Transmembrane Conductance Regulator

The Journal of biological chemistry, 2001-04, Vol.276 (16), p.12918-12923

2001

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Conformational Variability in Ground-State CFTR Lipoprotein Particle Cryo-EM Ensembles

Multiple Membrane-Cytoplasmic Domain Contacts in the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Mediate Regulation of Channel Gating

Purification and Crystallization of the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR)

Cryo-EM Visualization of an Active High Open Probability CFTR Anion Channel

R‑Domain Phosphorylation by Protein Kinase A Stimulates Dissociation of Unhydrolyzed ATP from the First Nucleotide-Binding Site of the Cystic Fibrosis Transmembrane Conductance Regulator

The cubicon method for concentrating membrane proteins in the cubic mesophase

Membrane protein stability can be compromised by detergent interactions with the extramembranous soluble domains

Allosteric Modulation Balances Thermodynamic Stability and Restores Function of ΔF508 CFTR

Restoration of domain folding and interdomain assembly by second-site suppressors of the ΔF508 mutation in CFTR

The cystic fibrosis transmembrane conductance regulator (CFTR): three-dimensional structure and localization of a channel gate

Thermal stability of purified and reconstituted CFTR in a locked open channel conformation

CFTR (ABCC7) is a hydrolyzable-ligand-gated channel

CFTR (ABCC7) is a hydrolyzable-ligand-gated channel

Architecture of the cystic fibrosis transmembrane conductance regulator protein and structural changes associated with phosphorylation and nucleotide binding

Regulatory Insertion Removal Restores Maturation, Stability and Function of ΔF508 CFTR

Do main location within the cystic fibrosis transmembrane conductance regulator protein investigated by electron microscopy and gold labelling

Multiple Membrane-Cytoplasmic Domain Contacts in the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Mediate Regulation of Channel GatingS

Domain location within the cystic fibrosis transmembrane conductance regulator protein investigated by electron microscopy and gold labelling

Restoration of domain folding and interdomain assembly by second-site suppressors of the DeltaF508 mutation in CFTR

Regulatory insertion removal restores maturation, stability and function of DeltaF508 CFTR

The First Nucleotide Binding Domain of Cystic Fibrosis Transmembrane Conductance Regulator Is a Site of Stable Nucleotide Interaction, whereas the Second Is a Site of Rapid Turnover

The role of cystic fibrosis transmembrane conductance regulator phenylalanine 508 side chain in ion channel gating

Domain Interdependence in the Biosynthetic Assembly of CFTR

The non-hydrolytic pathway of cystic fibrosis transmembrane conductance regulator ion channel gating

Differential Interactions of Nucleotides at the Two Nucleotide Binding Domains of the Cystic Fibrosis Transmembrane Conductance Regulator

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