Positioning of a peptide in the cleft of HLA-A2 by complementing amino acid changes

Proc Natl Acad Sci U S A. 1991 Dec 15;88(24):11325-9. doi: 10.1073/pnas.88.24.11325.

Abstract

Several mutant HLA-A2 molecules have been constructed and expressed in the mutant human B-cell line C1R, which lacks HLA-A and HLA-B antigens, and examined for presentation of a previously defined peptide epitope derived from the influenza matrix protein to appropriate human cytotoxic T-lymphocyte lines. When leucine residue 66 in this matrix peptide containing residues 57-68 (matrix peptide 57-68) was replaced by arginine, the resulting matrix peptide 57-68 R66 was not presented to HLA-A2, but the mutation Y116D (tyrosine to aspartic acid at residue 116) in the floor of the peptide binding cleft near its right end dramatically restored peptide presentation. A similar result was obtained by substitution of ornithine for leucine at residue 66. These data provide strong support for a model in which the peptide is orientated with its amino terminus at the left end of the cleft of HLA-A2 and its carboxyl terminus at the right.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Amino Acid Sequence
  • B-Lymphocytes / immunology
  • Binding Sites
  • Cell Line
  • Cloning, Molecular
  • Escherichia coli / genetics
  • HLA-A2 Antigen / genetics
  • HLA-A2 Antigen / immunology*
  • Humans
  • Influenza A virus / immunology
  • Models, Molecular
  • Molecular Sequence Data
  • Mutagenesis, Site-Directed
  • Peptide Fragments / immunology
  • Protein Conformation
  • Recombinant Proteins / immunology
  • T-Lymphocytes, Cytotoxic
  • Transfection
  • Viral Matrix Proteins / immunology*

Substances

  • HLA-A2 Antigen
  • Peptide Fragments
  • Recombinant Proteins
  • Viral Matrix Proteins