David M. Kranz

Jennifer D. Stone

K. Christopher Garcia

Leremy A. Colf

Lindsay L. Jones

Abstract
               T cells are known to cross-react with diverse peptide MHC Ags through their αβ TCR. To explore the basis of such cross-reactivity, we examined the 2C TCR that recognizes two structurally distinct ligands, SIY-Kb and alloantigen QL9-Ld. In this study we characterized the cross-reactivity of several high-affinity 2C TCR variants that contained mutations only in the CDR3α loop. Two of the TCR lost their ability to cross-react with the reciprocal ligand (SIY-Kb), whereas another TCR (m67) maintained reactivity with both ligands. Crystal structures of four of the TCRs in complex with QL9-Ld showed that CDR1, CDR2, and CDR3β conformations and docking orientations were remarkably similar. Although the CDR3α loop of TCR m67 conferred a 2000-fold higher affinity for SIY-Kb, the TCR maintained the same docking angle on QL9-Ld as the 2C TCR. Thus, CDR3α dictated the affinity and level of cross-reactivity, yet it did so without affecting the conserved docking orientation.</jats:p

Distinct CDR3 Conformations in TCRs Determine the Level of Cross-Reactivity for Diverse Antigens, but Not the Docking Orientation

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