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T cells use their T-cell receptors (TCRs) to discriminate between higher-affinity foreign and lower-affinity self-peptide-MHC (pMHC) antigen complexes. The OT-I mouse TCR is widely used to study antigen discrimination between foreign and self-pMHC antigens, and previous work suggested it achieved near-perfect discrimination between higher- and lower-affinity antigens. However, other TCRs show imperfect discrimination. To resolve these discrepancies, we developed in this study a protocol for measuring ultra-low TCR-pMHC binding affinities to determine the 3D solution affinities of OT-I TCR for 19 pMHCs. These revised 3D affinities now strongly correlate with 2D membrane affinities and predict T-cell functional responses. Our results indicate that OT-I exhibits enhanced yet imperfect discrimination, similar to other TCRs, explaining how T cells can detect abnormally high levels of low-affinity self-antigens. We also show that OT-I discrimination is consistent with the kinetic proofreading model, which highlights that discrimination is most effective for low-affinity pMHC ligands. Our work underscores the ability of T cells to gauge proxies for 3D affinity within the 2D interface, with implications for the mechanisms underlying antigen discrimination.

More information Original publication

DOI

10.1038/s44318-025-00644-5

Type

Journal article

Publication Date

2026-01-01T00:00:00+00:00

Volume

45

Pages

394 - 416

Total pages

22

Keywords

Affinity, Antigen Discrimination, OT-I TCR, Surface Plasmon Resonance, T cell, Animals, Mice, Receptors, Antigen, T-Cell, Autoantigens, T-Lymphocytes, Protein Binding