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Updated: Aug 6, 2026

Generating De Novo Antigen-specific Human T Cell Receptors by Retroviral Transduction of Centric Hemichain
Published on: October 25, 2016
Systematic analysis of CDR contacts and pairing constraints between T cell receptor αβ chains
Martina Milighetti1,2, Yuta Nagano1,3, James Henderson1,4
1Division of Infection and Immunity, University College London, London, WC1E 6BT, United Kingdom.
Motivation:
The six complementarity determining regions (CDRs) of the T cell receptor (TCR) form multiple contacts with cognate peptide and major histocompatibility complex, thus determining antigen specificity. However, the contacts between the CDRs themselves are less understood.
Results:
Our systematic study of all available TCR crystallographic structures identified consistent patterns of intra- and inter-chain CDR contacts in both free and antigen-bound TCRs. In addition, the protein sequences of TCRα and TCRβ from sets of TCRs which recognise a shared antigen shared mutual information and were not independent. As a result, sequence-based models can partially predict TCRα/TCRβ pairing de novo. The conserved patterns of CDR amino acid contacts, and the mutual sequence constraints between antigen-specific sets of TCR α and β chains represent an under-appreciated element of TCR structure, which may play an important role in T cell antigen recognition.
Availability And Implementation:
The code and data necessary to reproduce the analyses are available at https://github.com/mm523/TCRab-pairing.
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