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Hijacking the Fusion Complex of Human Parainfluenza Virus as an Antiviral Strategy

mBio, 2020-02, Vol.11 (1)

2020

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Human parainfluenza virus fusion complex glycoproteins imaged in action on authentic viral surfaces

PLoS pathogens, 2020-09, Vol.16 (9), p.e1008883-e1008883

2020

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Parainfluenza virus entry at the onset of infection

Advances in virus research, 2021, Vol.111, p.1

2021

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Inhibition of Measles Viral Fusion Is Enhanced by Targeting Multiple Domains of the Fusion Protein

ACS nano, 2021-08, Vol.15 (8), p.12794-12803

2021

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Human parainfluenza virus evolution during lung infection of immunocompromised individuals promotes viral persistence

The Journal of clinical investigation, 2021-12, Vol.131 (23)

2021

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Single-chain variable fragment antibody constructs neutralize measles virus infection in vitro and in vivo

Cellular & molecular immunology, 2021-07, Vol.18 (7), p.1835-1837

2021

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Transient Collagen Triple Helix Binding to a Key Metalloproteinase in Invasion and Development

Structure (London), 2015-02, Vol.23 (2), p.257-269

2015

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Peripheral membrane associations of matrix metalloproteinases

Biochimica et biophysica acta. Molecular cell research, 2017-11, Vol.1864 (11), p.1964-1973

2017

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A neutralizing antibody prevents postfusion transition of measles virus fusion protein

Science (American Association for the Advancement of Science), 2024-06, Vol.384 (6703), p.eadm8693

2024

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Host Cell Membrane Capture by the SARS-CoV‑2 Spike Protein Fusion Intermediate

ACS central science, 2023-06, Vol.9 (6), p.1213-1228

2023

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MT1-MMP Binds Membranes by Opposite Tips of Its β Propeller to Position It for Pericellular Proteolysis

Structure (London), 2019-02, Vol.27 (2), p.281-292.e6

2019

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Intermediates in SARS-CoV-2 spike-mediated cell entry

Science advances, 2022-08, Vol.8 (33), p.eabo3153-eabo3153

2022

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Subnanometer structure of an enveloped virus fusion complex on viral surface reveals new entry mechanisms

Science advances, 2023-02, Vol.9 (6), p.eade2727-eade2727

2023

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Mapping Lipid Bilayer Recognition Sites of Metalloproteinases and Other Prospective Peripheral Membrane Proteins

Methods in molecular biology (Clifton, N.J.), 2017, Vol.1579, p.61

2017

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Membrane Interactions of the Protease MT1-MMP

Biophysical journal, 2018-02, Vol.114 (3), p.237a-237a

2018

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Transient Interactions of Metalloproteinases with Bilayers, Captured by Paramagnetic NMR, Include Dual Modes of Binding, Electrostatic Recruiting, and Allostery

Biophysical journal, 2017-02, Vol.112 (3), p.478a-478a

2017

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Chemical shift assignments of domain 4 from the phosphohexomutase from Pseudomonas aeruginosa suggest that freeing perturbs its coevolved domain interface

Biomolecular NMR assignments, 2014-10, Vol.8 (2), p.329-333

2014

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Hijacking the Fusion Complex of Human Parainfluenza Virus as an Antiviral Strategy

Human parainfluenza virus fusion complex glycoproteins imaged in action on authentic viral surfaces

Parainfluenza virus entry at the onset of infection

Inhibition of Measles Viral Fusion Is Enhanced by Targeting Multiple Domains of the Fusion Protein

Human parainfluenza virus evolution during lung infection of immunocompromised individuals promotes viral persistence

Single-chain variable fragment antibody constructs neutralize measles virus infection in vitro and in vivo

Transient Collagen Triple Helix Binding to a Key Metalloproteinase in Invasion and Development

Peripheral membrane associations of matrix metalloproteinases

A neutralizing antibody prevents postfusion transition of measles virus fusion protein

Host Cell Membrane Capture by the SARS-CoV‑2 Spike Protein Fusion Intermediate

MT1-MMP Binds Membranes by Opposite Tips of Its β Propeller to Position It for Pericellular Proteolysis

Intermediates in SARS-CoV-2 spike-mediated cell entry

Subnanometer structure of an enveloped virus fusion complex on viral surface reveals new entry mechanisms

Mapping Lipid Bilayer Recognition Sites of Metalloproteinases and Other Prospective Peripheral Membrane Proteins

Membrane Interactions of the Protease MT1-MMP

Transient Interactions of Metalloproteinases with Bilayers, Captured by Paramagnetic NMR, Include Dual Modes of Binding, Electrostatic Recruiting, and Allostery

Chemical shift assignments of domain 4 from the phosphohexomutase from Pseudomonas aeruginosa suggest that freeing perturbs its coevolved domain interface

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