Alteration within a discrete region of the H-2Ld alpha 1 helix upon association with human beta 2 microglobulin

Immunol Cell Biol. 1993 Apr:71 ( Pt 2):145-9. doi: 10.1038/icb.1993.16.

Abstract

The utilization of the beta 2-microglobulin (B2m) exchange assay allowed for the association of H-2Ld with human B2m. Upon association with H-2Ld, human B2m induces structural alterations in H-2Ld that appear dependent upon xenogeneic B2m amino acid sequence variability. In this regard, xenogeneic B2m exchange is used as a tool to induce structural alterations in class I as a means of analysing the structural-functional relationship of B2m/class I association. Incorporating H-2Ld site-directed mutants into the experimental approach provided strong evidence that B2m makes indirect contact with discrete class I specific amino acid positions located in the helical region of the alpha 1 domain.

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Binding Sites
  • Cell Line
  • H-2 Antigens / chemistry
  • H-2 Antigens / genetics
  • H-2 Antigens / metabolism*
  • Histocompatibility Antigen H-2D
  • Humans
  • Mice
  • Molecular Sequence Data
  • Mutagenesis, Site-Directed
  • Protein Binding
  • Protein Structure, Secondary
  • beta 2-Microglobulin / metabolism*

Substances

  • H-2 Antigens
  • Histocompatibility Antigen H-2D
  • beta 2-Microglobulin