Journal article
Murine T-cell receptor OT-I exhibits imperfect discrimination between foreign and self-antigens
- Abstract:
- 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.
- Publication status:
- Published
- Peer review status:
- Peer reviewed
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(Preview, Version of record, pdf, 1.7MB, Terms of use)
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- Publisher copy:
- 10.1038/s44318-025-00644-5
Authors
- Publisher:
- EMBO Press
- Journal:
- The EMBO Journal More from this journal
- Volume:
- 45
- Issue:
- 2
- Pages:
- 394-416
- Publication date:
- 2025-11-26
- Acceptance date:
- 2025-10-17
- DOI:
- EISSN:
-
1460-2075
- ISSN:
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0261-4189
- Language:
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English
- Keywords:
- Pubs id:
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2338660
- UUID:
-
uuid_2b0b6490-971e-4b64-9932-c866430d2529
- Local pid:
-
pubs:2338660
- Source identifiers:
-
3668323
- Deposit date:
-
2026-01-16
- ARK identifier:
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Terms of use
- Copyright date:
- 2025
- Licence:
- CC Attribution (CC BY)
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