Determination of interaction kinetics between the T cell receptor and peptide-loaded MHC class II via single-molecule diffusion measurements
- PMID: 22853916
- PMCID: PMC3400783
- DOI: 10.1016/j.bpj.2012.06.019
Determination of interaction kinetics between the T cell receptor and peptide-loaded MHC class II via single-molecule diffusion measurements
Abstract
The binding of peptide-loaded major histocompatibility complex (pMHC) to the T cell receptor (TCR) represents the central step in T cell antigen recognition. It proceeds in the cell contact area between a T cell and an antigen-presenting cell termed the immunological synapse. An important and unresolved issue is how T cells discriminate between potentially harmful and harmless antigens. One limitation has been the difficulty to measure interaction parameters directly, that is, as they occur in the immunological synapse. Here we present a single-molecule approach to determine pMHC-TCR interaction kinetics in situ based on diffusion analysis of dye-labeled pMHC. We find synaptic off-rates >10-fold accelerated when compared to the dissociation of purified proteins measured in vitro.
Copyright © 2012 Biophysical Society. Published by Elsevier Inc. All rights reserved.
Figures
References
-
- Grakoui A., Bromley S.K., Dustin M.L. The immunological synapse: a molecular machine controlling T cell activation. Science. 1999;285:221–227. - PubMed
-
- Irvine D.J., Purbhoo M.A., Davis M.M. Direct observation of ligand recognition by T cells. Nature. 2002;419:845–849. - PubMed
-
- Tian S., Maile R., Frelinger J.A. CD8+ T cell activation is governed by TCR-peptide/MHC affinity, not dissociation rate. J. Immunol. 2007;179:2952–2960. - PubMed
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Molecular Biology Databases
Research Materials
