Modification of MHC Anchor Residues Generates Heteroclitic Peptides That Alter TCR Binding and T Cell Recognition

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Structural basis for ineffective T-cell responses to MHC anchor residue-improved “heteroclitic” peptides

T-cell Receptor Specificity Maintained by Altered Thermodynamics

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Increased peptide contacts govern high affinity binding of a modified TCR whilst maintaining a native pMHC docking mode

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γδ T Cell Receptors Recognize the Non-classical Major Histocompatibility Complex (MHC) Molecule T22 via Conserved Anchor Residues in a MHC Peptide-like Fashion

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Structural basis for the restoration of tcr recognition of an mhc allelic variant by peptide secondary anchor substitution.

T Cell Activity Correlates with Oligomeric Peptide-Major Histocompatibility Complex Binding on T Cell Surface

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Recognition of multiple peptide cores by a single t cell receptor.

Discriminative T-cell receptor recognition of highly homologous HLA-DQ2–bound gluten epitopes

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