Mimicry of an HIV broadly neutralizing antibody epitope with a synthetic glycopeptide. Academic Article uri icon

Overview

abstract

  • A goal for an HIV-1 vaccine is to overcome virus variability by inducing broadly neutralizing antibodies (bnAbs). One key target of bnAbs is the glycan-polypeptide at the base of the envelope (Env) third variable loop (V3). We have designed and synthesized a homogeneous minimal immunogen with high-mannose glycans reflective of a native Env V3-glycan bnAb epitope (Man9-V3). V3-glycan bnAbs bound to Man9-V3 glycopeptide and native-like gp140 trimers with similar affinities. Fluorophore-labeled Man9-V3 glycopeptides bound to bnAb memory B cells and were able to be used to isolate a V3-glycan bnAb from an HIV-1-infected individual. In rhesus macaques, immunization with Man9-V3 induced V3-glycan-targeted antibodies. Thus, the Man9-V3 glycopeptide closely mimics an HIV-1 V3-glycan bnAb epitope and can be used to isolate V3-glycan bnAbs.

authors

publication date

  • March 15, 2017

Research

keywords

  • Antibodies, Neutralizing
  • Epitopes
  • Glycopeptides
  • HIV-1
  • Molecular Mimicry

Identity

PubMed Central ID

  • PMC5562351

Scopus Document Identifier

  • 85016422011

Digital Object Identifier (DOI)

  • 10.1126/scitranslmed.aai7521

PubMed ID

  • 28298421

Additional Document Info

volume

  • 9

issue

  • 381