Isolation of HLA-DR1.(staphylococcal enterotoxin A)2 trimers in solution

Proc Natl Acad Sci U S A. 1995 Dec 19;92(26):12156-9. doi: 10.1073/pnas.92.26.12156.

Abstract

Mutational studies indicate that the superantigen staphylococcal enterotoxin A (SEA) has two separate binding sites for major histocompatibility complex (MHC) class II molecules. Direct evidence is provided here for the formation of SEA-MHC class II trimers in solution. Isoelectric focusing separated SEA-HLA-DR1 complexes into both dimers and HLA-DR1.SEA2 trimers. The molar ratio of components was determined by dual isotope labeling. The SEA mutant SEA-F47S, L48S, Y92A, which is deficient in MHC class II alpha-chain binding, formed only dimers with HLA-DR1, whereas a second SEA mutant, SEA-H225A, which lacks high-affinity MHC class II beta-chain binding was incapable of forming any complexes. Thus SEA binding to its MHC receptor is a two-step process involving initial beta-chain binding followed by cooperative binding of a second SEA molecule to the class II alpha chain.

MeSH terms

  • B-Lymphocytes
  • Binding Sites
  • Cell Line
  • Enterotoxins / chemistry*
  • Enterotoxins / immunology*
  • Enterotoxins / isolation & purification
  • HLA-DR1 Antigen / chemistry*
  • HLA-DR1 Antigen / isolation & purification
  • Humans
  • Isoelectric Focusing
  • Macromolecular Substances
  • Models, Structural
  • Protein Structure, Secondary*
  • Recombinant Proteins / chemistry
  • Recombinant Proteins / immunology
  • Recombinant Proteins / isolation & purification
  • Solutions
  • Staphylococcus aureus / immunology
  • Superantigens / chemistry
  • Superantigens / immunology
  • Superantigens / isolation & purification
  • Zinc Fingers

Substances

  • Enterotoxins
  • HLA-DR1 Antigen
  • Macromolecular Substances
  • Recombinant Proteins
  • Solutions
  • Superantigens
  • enterotoxin A, Staphylococcal