articleJournal of VirologyJul 15, 2002GREEN OA

The Broadly Neutralizing Anti-Human Immunodeficiency Virus Type 1 Antibody 2G12 Recognizes a Cluster of α1→2 Mannose Residues on the Outer Face of gp120

University of Oxford · Scripps Research Institute

PubMed
Indexed incrossrefdoajpubmed

Abstract

2G12 is a broadly neutralizing human monoclonal antibody against human immunodeficiency virus type-1 (HIV-1) that has previously been shown to bind to a carbohydrate-dependent epitope on gp120. Here, site-directed mutagenesis and carbohydrate analysis were used to define further the 2G12 epitope. Extensive alanine scanning mutagenesis showed that elimination of the N-linked carbohydrate attachment sequences associated with residues N295, N332, N339, N386, and N392 by N-->A substitution produced significant decreases in 2G12 binding affinity to gp120(JR-CSF). Further mutagenesis suggested that the glycans at N339 and N386 were not critical for 2G12 binding to gp120(JR-CSF). Comparison of the sequences of…

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Authors

10

Topics & keywords

Keywords
  • Epitope
  • Glycan
  • Biology
  • Mannose
  • Biochemistry
  • Mutagenesis
  • Binding site
  • Site-directed mutagenesis
UN Sustainable Development Goals
  • Good health and well-being
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