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Detection of intermolecular NOE interactions in large protein complexes

Progress in nuclear magnetic resonance spectroscopy, 2016-11, Vol.97, p.40-56

2016

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Peptides in the treatment of AIDS

Current opinion in structural biology, 2009-08, Vol.19 (4), p.473-482

2009

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Molecular Switch for Alternative Conformations of the HIV-1 V3 Region: Implications for Phenotype Conversion

Proceedings of the National Academy of Sciences - PNAS, 2006-09, Vol.103 (38), p.13950-13955

2006

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Observation of Intermolecular Interactions in Large Protein Complexes by 2D-Double Difference Nuclear Overhauser Enhancement Spectroscopy: Application to the 44 kDa Interferon–Receptor Complex

Journal of the American Chemical Society, 2011-09, Vol.133 (37), p.14755-14764

2011

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Intermolecular Interactions in a 44 kDa Interferon−Receptor Complex Detected by Asymmetric Reverse-Protonation and Two-Dimensional NOESY

Biochemistry (Easton), 2010-06, Vol.49 (25), p.5117-5133

2010

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Solid-State NMR Yields Structural Constraints on the V3 Loop from HIV-1 Gp120 Bound to the 447-52D Antibody Fv Fragment

Journal of the American Chemical Society, 2004-04, Vol.126 (15), p.4979-4990

2004

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Determination of the human type I interferon receptor binding site on human interferon‐α2 by cross saturation and an NMR‐based model of the complex

Protein science, 2006-11, Vol.15 (11), p.2656-2668

2006

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The chemokines CCL5 and CXCL12 exhibit high‐affinity binding to N‐terminal peptides of the non‐cognate receptors CXCR4 and CCR5, respectively

The FEBS journal, 2024-02, Vol.291 (3), p.458-476

2024

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Multiple binding modes of an N‐terminal CCR5‐peptide in complex with HIV‐1 gp120

The FEBS journal, 2022-06, Vol.289 (11), p.3132-3147

2022

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Detection of intermolecular transferred‐NOE interactions in small and medium size protein complexes: RANTES complexed with a CCR5 N‐terminal peptide

The FEBS journal, 2017-02, Vol.284 (4), p.586-601

2017

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Defining specific residue‐to‐residue interactions between the gp120 bridging sheet and the N‐terminal segment of CCR5: applications of transferred NOE NMR

The FEBS journal, 2018-11, Vol.285 (22), p.4296-4310

2018

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Defining specific residue‐to‐residue interactions between the gp120 bridging sheet and the N‐terminal segment of CCR 5: applications of transferred NOE NMR

The FEBS journal, 2018-11, Vol.285 (22), p.4296-4310

2018

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Allovalency observed by transferred NOE: interactions of sulfated tyrosine residues in the N‐terminal segment of CCR5 with the CCL5 chemokine

The FEBS journal, 2021-03, Vol.288 (5), p.1648-1663

2021

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The solution structure of monomeric CCL5 in complex with a doubly sulfated N‐terminal segment of CCR5

The FEBS journal, 2018-06, Vol.285 (11), p.1988-2003

2018

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Immunofocusing using conformationally constrained V3 peptide immunogens improves HIV-1 neutralization

Vaccine, 2017-01, Vol.35 (2), p.222-230

2017

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C4 region as a target for HIV entry inhibitors – NMR mapping of the interacting segments of T20 and gp120

The FEBS journal, 2015-12, Vol.282 (24), p.4643-4657

2015

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Detection of intermolecular transferred NOEs in large protein complexes using asymmetric deuteration: HIV‐1 gp120 in complex with a CCR5 peptide

The FEBS journal, 2016-11, Vol.283 (22), p.4084-4096

2016

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Detection of intermolecular transferred NOE s in large protein complexes using asymmetric deuteration: HIV ‐1 gp120 in complex with a CCR 5 peptide

The FEBS journal, 2016-11, Vol.283 (22), p.4084-4096

2016

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extended CCR5 ECL2 peptide forms a helix that binds HIV‐1 gp120 through non‐specific hydrophobic interactions

The FEBS journal, 2015-05, Vol.282 (10), p.1906-1921

2015

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The solution structure of monomeric CCL 5 in complex with a doubly sulfated N‐terminal segment of CCR 5

The FEBS journal, 2018-06, Vol.285 (11), p.1988-2003

2018

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An extended CCR 5 ECL 2 peptide forms a helix that binds HIV ‐1 gp120 through non‐specific hydrophobic interactions

The FEBS journal, 2015-05, Vol.282 (10), p.1906-1921

2015

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An optimally constrained V3 peptide is a better immunogen than its linear homolog or HIV-1 gp120

Virology (New York, N.Y.), 2010-06, Vol.401 (2), p.293-304

2010

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Epitope mapping of antibody-antigen complexes by nuclear magnetic resonance spectroscopy

Methods in molecular biology (Clifton, N.J.), 2009, Vol.524, p.37

2009

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The Membrane Proximal External Region of the HIV-1 Envelope Glycoprotein gp41 Contributes to the Stabilization of the Six-Helix Bundle Formed with a Matching N′ Peptide

Biochemistry (Easton), 2008-07, Vol.47 (26), p.6782-6792

2008

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Alternative Conformations of HIV-1 V3 Loops Mimic β Hairpins in Chemokines, Suggesting a Mechanism for Coreceptor Selectivity

Structure (London), 2003-02, Vol.11 (2), p.225-236

2003

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Detection of intermolecular NOE interactions in large protein complexes

Peptides in the treatment of AIDS

Molecular Switch for Alternative Conformations of the HIV-1 V3 Region: Implications for Phenotype Conversion

Observation of Intermolecular Interactions in Large Protein Complexes by 2D-Double Difference Nuclear Overhauser Enhancement Spectroscopy: Application to the 44 kDa Interferon–Receptor Complex

Intermolecular Interactions in a 44 kDa Interferon−Receptor Complex Detected by Asymmetric Reverse-Protonation and Two-Dimensional NOESY

Solid-State NMR Yields Structural Constraints on the V3 Loop from HIV-1 Gp120 Bound to the 447-52D Antibody Fv Fragment

Determination of the human type I interferon receptor binding site on human interferon‐α2 by cross saturation and an NMR‐based model of the complex

The chemokines CCL5 and CXCL12 exhibit high‐affinity binding to N‐terminal peptides of the non‐cognate receptors CXCR4 and CCR5, respectively

Multiple binding modes of an N‐terminal CCR5‐peptide in complex with HIV‐1 gp120

Detection of intermolecular transferred‐NOE interactions in small and medium size protein complexes: RANTES complexed with a CCR5 N‐terminal peptide

Defining specific residue‐to‐residue interactions between the gp120 bridging sheet and the N‐terminal segment of CCR5: applications of transferred NOE NMR

Defining specific residue‐to‐residue interactions between the gp120 bridging sheet and the N‐terminal segment of CCR 5: applications of transferred NOE NMR

Allovalency observed by transferred NOE: interactions of sulfated tyrosine residues in the N‐terminal segment of CCR5 with the CCL5 chemokine

The solution structure of monomeric CCL5 in complex with a doubly sulfated N‐terminal segment of CCR5

Immunofocusing using conformationally constrained V3 peptide immunogens improves HIV-1 neutralization

C4 region as a target for HIV entry inhibitors – NMR mapping of the interacting segments of T20 and gp120

Detection of intermolecular transferred NOEs in large protein complexes using asymmetric deuteration: HIV‐1 gp120 in complex with a CCR5 peptide

Detection of intermolecular transferred NOE s in large protein complexes using asymmetric deuteration: HIV ‐1 gp120 in complex with a CCR 5 peptide

extended CCR5 ECL2 peptide forms a helix that binds HIV‐1 gp120 through non‐specific hydrophobic interactions

The solution structure of monomeric CCL 5 in complex with a doubly sulfated N‐terminal segment of CCR 5

An extended CCR 5 ECL 2 peptide forms a helix that binds HIV ‐1 gp120 through non‐specific hydrophobic interactions

An optimally constrained V3 peptide is a better immunogen than its linear homolog or HIV-1 gp120

Epitope mapping of antibody-antigen complexes by nuclear magnetic resonance spectroscopy

The Membrane Proximal External Region of the HIV-1 Envelope Glycoprotein gp41 Contributes to the Stabilization of the Six-Helix Bundle Formed with a Matching N′ Peptide

Alternative Conformations of HIV-1 V3 Loops Mimic β Hairpins in Chemokines, Suggesting a Mechanism for Coreceptor Selectivity

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