Paired heavy- and light-chain signatures contribute to potent SARS-CoV-2 neutralization in public antibody responses

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Rapid isolation and profiling of a diverse panel of human monoclonal antibodies targeting the SARS-CoV-2 spike protein

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A neutralizing human antibody binds to the N-terminal domain of the Spike protein of SARS-CoV-2

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Potent neutralizing antibodies from COVID-19 patients define multiple targets of vulnerability

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Structural and Functional Analysis of the D614G SARS-CoV-2 Spike Protein Variant

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Structurally Resolved SARS-CoV-2 Antibody Shows High Efficacy in Severely Infected Hamsters and Provides a Potent Cocktail Pairing Strategy

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UCSF ChimeraX : Structure visualization for researchers, educators, and developers

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Ultrapotent human antibodies protect against SARS-CoV-2 challenge via multiple mechanisms

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An Alternative Binding Mode of IGHV3-53 Antibodies to the SARS-CoV-2 Receptor Binding Domain

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Evaluating the Effects of SARS-CoV-2 Spike Mutation D614G on Transmissibility and Pathogenicity

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Cryo-EM Structures of SARS-CoV-2 Spike without and with ACE2 Reveal a pH-Dependent Switch to Mediate Endosomal Positioning of Receptor-Binding Domains

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The Panitumumab EGFR Complex Reveals a Binding Mechanism That Overcomes Cetuximab Induced Resistance

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In-depth determination and analysis of the human paired heavy- and light-chain antibody repertoire

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Multidonor Analysis Reveals Structural Elements, Genetic Determinants, and Maturation Pathway for HIV-1 Neutralization by VRC01-Class Antibodies

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