Early biochemical signals arise from low affinity TCR-ligand reactions at the cell-cell interface

Craig Beeson, Josh Rabinowitz, Keri Tate, Ines Gütgemann, Yueh Hsiu Chien, Patricia P. Jones, Mark M. Davis, Harden M. McConnell

Research output: Contribution to journalArticlepeer-review

52 Scopus citations


The kinetics of acid release by a mixture of T cells and antigen presenting cells were measured with a microphysiometer during a brief exposure to antigenic peptides. We find that some of the early biochemical events that lead to cellular proliferation cause a specific increase in the rate of acid release. The duration of this increase in acid release reflects the life-time of the peptide-MHC complexes. Peptides that form long-live complexes produce a response that is stable for more than an hour. Serial TCR engagement is suggested by the observation that the amplitude of this stable response can be rapidly shifted up or down with additional agonist peptide or with antibodies that block T cell receptor binding. Cells briefly exposed to a peptide that forms short-lived peptide-MHC complexes produce a response that decays rapidly as peptide is washed away. A quantitative analysis of the kinetics of this decay in acidification demonstrates that intercellular TCR- ligand reactions are rapid, reversible, and of flow apparent affinity with >20% of peptide-MHC ligand bound to a TCR at any one time. These results demonstrates that the fraction of peptide-MHC ligand bound to TCRs at the cell-cell interface is no higher than anticipated from the affinities observed in solution for isolated TCRs and ligand.

Original languageEnglish (US)
Pages (from-to)777-782
Number of pages6
JournalJournal of Experimental Medicine
Issue number2
StatePublished - Aug 1 1996
Externally publishedYes

All Science Journal Classification (ASJC) codes

  • Immunology and Allergy
  • Immunology


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