Interaction between a "processed" ovalbumin peptide and Ia molecules

Proc Natl Acad Sci U S A. 1986 Jun;83(11):3968-71. doi: 10.1073/pnas.83.11.3968.

Abstract

The binding of 125I-labeled immunogenic peptides to purified Ia molecules in detergent solution was examined by equilibrium dialysis. We used the chicken ovalbumin peptide ovalbumin-(323-339)-Tyr, which is immunogenic in the BALB/c mouse and restricted to I-Ad. 125I-labeled ovalbumin-(323-339)-Tyr was shown to bind to I-Ad but not to I-Ed, I-Ek, or I-Ak. This binding was inhibited by unlabeled ovalbumin-(323-339) but not by ovalbumin-(329-339), which is the longest N-terminally truncated peptide that fails to stimulate any of the I-Ad-restricted hybridomas that have been raised to ovalbumin-(323-339)-Tyr. As a further specificity control, we also used the chicken egg lysozyme peptide Tyr-(46-61), which has recently been studied by similar methods [Babbitt, B. P., Allen, P. M., Matsueda, G., Haber, E. & Unanue, E. R. (1985) Nature (London) 317, 359-361]. We have confirmed that it bound to I-Ak but not to I-Ek, I-Ad, or I-Ed. Thus, a specific interaction between Ia and antigen that correlates with the major histocompatibility complex restriction was demonstrated, strongly arguing in favor of a determinant selection hypothesis for such restriction.

Publication types

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

MeSH terms

  • Animals
  • Antigen-Presenting Cells / immunology
  • B-Lymphocytes / immunology
  • Histocompatibility Antigens Class II / immunology*
  • Mice
  • Ovalbumin / immunology*
  • Ovalbumin / metabolism
  • Peptide Fragments / immunology
  • Peptide Fragments / metabolism
  • Protein Binding
  • T-Lymphocytes / immunology*

Substances

  • Histocompatibility Antigens Class II
  • Peptide Fragments
  • Ovalbumin