Mapping and characterization of B cell linear epitopes in the conservative regions of hepatitis C virus envelope glycoproteins

J Viral Hepat. 2002 May;9(3):174-82. doi: 10.1046/j.1365-2893.2002.00358.x.

Abstract

Forty-eight overlapping octapeptides covering highly conservative regions of E1 and E2 hepatitis C virus (HCV) envelope proteins were synthesized and tested by ELISA against different groups of sera obtained from HCV-infected patients. All sera from patients with acute infection, except a single case of serum reactivity with the region HINRTALN, were nonreactive with any peptide. Sera obtained from chronic patients reacted with 12 peptides from five selected regions. Two immunodominant B epitopes were found, one being the precisely mapped antigenic site RMAWDM positioned inside the earlier shown immunodominant epitope from E1, and the second site, PALSTGLIH from E2, detected for the first time. New minor antigenic site was determined as PTDCFRKH from E2. We found only minor seroreactivity for one of the putative sites involved in CD81 binding, PYCWHYAP.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Amino Acid Sequence
  • B-Lymphocytes / immunology*
  • Binding, Competitive
  • Child, Preschool
  • Conserved Sequence*
  • Epitope Mapping*
  • Hepacivirus / immunology
  • Hepatitis C / immunology
  • Hepatitis C Antibodies / metabolism
  • Humans
  • Middle Aged
  • Molecular Sequence Data
  • Peptides / chemical synthesis
  • Peptides / chemistry
  • Peptides / immunology
  • Peptides / metabolism
  • Viral Envelope Proteins / chemistry
  • Viral Envelope Proteins / immunology*
  • Viral Envelope Proteins / metabolism

Substances

  • E1 protein, Hepatitis C virus
  • Hepatitis C Antibodies
  • Peptides
  • Viral Envelope Proteins
  • glycoprotein E2, Hepatitis C virus