Plasticity in the contribution of T cell receptor variable region residues to binding of peptide-HLA-A2 complexes

Sheena N. Smith, Daniel Sommermeyer, Kurt H. Piepenbrink, Sydney J. Blevins, Helga Bernhard, Wolfgang Uckert, Brian M. Baker, David M Kranz

Research output: Contribution to journalArticle

Abstract

One hypothesis accounting for major histocompatibility complex (MHC) restriction by T cell receptors (TCRs) holds that there are several evolutionary conserved residues in TCR variable regions that contact MHC. While this "germline codon" hypothesis is supported by various lines of evidence, it has been difficult to test. The difficulty stems in part from the fact that TCRs exhibit low affinities for pep/MHC, thus limiting the range of binding energies that can be assigned to these key interactions using mutational analyses. To measure the magnitude of binding energies involved, here we used high-affinity TCRs engineered by mutagenesis of CDR3. The TCRs included a high-affinity, MART-1/HLA-A2-specific single-chain TCR and two other high-affinity TCRs that all contain the same Vα region and recognize the same MHC allele (HLA-A2), with different peptides and Vβ regions. Mutational analysis of residues in CDR1 and CDR2 of the three Vα2 regions showed the importance of the key germline codon residue Y51. However, two other proposed key residues showed significant differences among the TCRs in their relative contributions to binding. With the use of single-position, yeast-display libraries in two of the key residues, MART-1/HLA-A2 selections also revealed strong preferences for wild-type germline codon residues, but several alternative residues could also accommodate binding and, hence, MHC restriction. Thus, although a single residue (Y51) could account for a proportion of the energy associated with positive selection (i.e., MHC restriction), there is significant plasticity in requirements for particular side chains in CDR1 and CDR2 and in their relative binding contributions among different TCRs.

Original languageEnglish (US)
Pages (from-to)4496-4507
Number of pages12
JournalJournal of Molecular Biology
Volume425
Issue number22
DOIs
StatePublished - Nov 15 2013

Fingerprint

HLA-A2 Antigen
T-Cell Antigen Receptor
Major Histocompatibility Complex
Peptides
Codon
Mutagenesis
Yeasts
Alleles

Keywords

  • T cell receptors
  • directed evolution
  • germline codon bias
  • single-chain
  • yeast display

ASJC Scopus subject areas

  • Molecular Biology

Cite this

Plasticity in the contribution of T cell receptor variable region residues to binding of peptide-HLA-A2 complexes. / Smith, Sheena N.; Sommermeyer, Daniel; Piepenbrink, Kurt H.; Blevins, Sydney J.; Bernhard, Helga; Uckert, Wolfgang; Baker, Brian M.; Kranz, David M.

In: Journal of Molecular Biology, Vol. 425, No. 22, 15.11.2013, p. 4496-4507.

Research output: Contribution to journalArticle

Smith, SN, Sommermeyer, D, Piepenbrink, KH, Blevins, SJ, Bernhard, H, Uckert, W, Baker, BM & Kranz, DM 2013, 'Plasticity in the contribution of T cell receptor variable region residues to binding of peptide-HLA-A2 complexes' Journal of Molecular Biology, vol. 425, no. 22, pp. 4496-4507. https://doi.org/10.1016/j.jmb.2013.08.007
Smith, Sheena N. ; Sommermeyer, Daniel ; Piepenbrink, Kurt H. ; Blevins, Sydney J. ; Bernhard, Helga ; Uckert, Wolfgang ; Baker, Brian M. ; Kranz, David M. / Plasticity in the contribution of T cell receptor variable region residues to binding of peptide-HLA-A2 complexes. In: Journal of Molecular Biology. 2013 ; Vol. 425, No. 22. pp. 4496-4507.
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