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Publications by D. Kabat

Kinetic Mechanism for HIV-1 Neutralization by Antibody 2G12 Entails Reversible Glycan Binding That Slows Cell Entry

Proceedings of the National Academy of Sciences of the United States of America

Multidisciplinary

2012

English

Rapid Dissociation of HIV-1 From Cultured Cells Severely Limits Infectivity Assays, Causes the Inactivation Ascribed to Entry Inhibitors, and Masks the Inherently High Level of Infectivity of Virions

English

Related publications

Glycan Microheterogeneity at the PGT135 Antibody Recognition Site on HIV-1 Gp120 Reveals a Molecular Mechanism for Neutralization Resistance

English

Antibody 2G12 Recognizes Di-Mannose Equivalently in Domain- And Nondomain-Exchanged Forms but Only Binds the HIV-1 Glycan Shield if Domain Exchanged

English

Potent and Broad Neutralization of HIV-1 by a Llama Antibody Elicited by Immunization

Journal of Experimental Medicine

English

Structural Basis for Diverse N-Glycan Recognition by HIV-1–neutralizing V1–V2–directed Antibody PG16

Nature Structural and Molecular Biology

Structural Biology

Molecular Biology

2013

English

Mechanisms of Human Immunodeficiency Virus Type 1 (HIV-1) Neutralization: Irreversible Inactivation of Infectivity by Anti-Hiv-1 Antibody.

English

Structural Basis for Broad HIV-1 Neutralization by a Novel MPER-Specific Human Broadly Neutralizing Antibody

SSRN Electronic Journal

2019

English

P04-06. Evolution of an Anti-Mper Gp41 Antibody Response That Mediates Broad HIV-1 Cross-Neutralization

English

Glycan Modulation and Sulfoengineering of Anti–HIV-1 Monoclonal Antibody PG9 in Plants

Proceedings of the National Academy of Sciences of the United States of America

Multidisciplinary

2015

English

The Mechanism of HIV Entry Inhibition by 25-Hydroxycholesterol

Biophysical Journal

Biophysics

2016

English

Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

Publications by D. Kabat

Kinetic Mechanism for HIV-1 Neutralization by Antibody 2G12 Entails Reversible Glycan Binding That Slows Cell Entry

Rapid Dissociation of HIV-1 From Cultured Cells Severely Limits Infectivity Assays, Causes the Inactivation Ascribed to Entry Inhibitors, and Masks the Inherently High Level of Infectivity of Virions

Related publications

Glycan Microheterogeneity at the PGT135 Antibody Recognition Site on HIV-1 Gp120 Reveals a Molecular Mechanism for Neutralization Resistance

Antibody 2G12 Recognizes Di-Mannose Equivalently in Domain- And Nondomain-Exchanged Forms but Only Binds the HIV-1 Glycan Shield if Domain Exchanged

Potent and Broad Neutralization of HIV-1 by a Llama Antibody Elicited by Immunization

Structural Basis for Diverse N-Glycan Recognition by HIV-1–neutralizing V1–V2–directed Antibody PG16

Mechanisms of Human Immunodeficiency Virus Type 1 (HIV-1) Neutralization: Irreversible Inactivation of Infectivity by Anti-Hiv-1 Antibody.

Structural Basis for Broad HIV-1 Neutralization by a Novel MPER-Specific Human Broadly Neutralizing Antibody

P04-06. Evolution of an Anti-Mper Gp41 Antibody Response That Mediates Broad HIV-1 Cross-Neutralization

Glycan Modulation and Sulfoengineering of Anti–HIV-1 Monoclonal Antibody PG9 in Plants

The Mechanism of HIV Entry Inhibition by 25-Hydroxycholesterol