Table 2.
T-cell clones respond to register-fixed DQ8/Ins complexes in R3
| DQ8-Ins | Peptide* | T1D#10 C8† | T1D#3 C8 | T1D#4 C5 |
| I72C-R1 | LEEALYLVAEEC | — | — | — |
| I72C-R2 | VEALYLVAGERC | — | — | — |
| I72C-R3 | VEELYLVAGEEGC | 1.5 | 31.6 | 4.9 |
| I72C-R4 | VEAEYLVAGEREGC | — | 0.4 | 0.1 |
| V65C-R1 | LEEALYCVAEER | — | — | — |
| V65C-R2 | VEALYLCAGERG | — | — | — |
| V65C-R3 | VEELYLVCGEEGG | 2.3 | 38.8 | 0.4 |
| V65C-R4 | VEAEYLVACEREGG | — | — | — |
The lowest concentration of IFN-γ standard was 0.017 ng/mL and readings below this level are indicated as with an “—.”
To “trap” each peptide in a specific register, corresponding p1 and p9 anchor residues of the peptide were mutated to E (in bold). To “fix” the peptide in a specific register by disulfide bonding, each set of peptides had a single C residue (underlined) at position p6 (to bind to V65C) or at p11 (to bind to I72C). The other C residue that would not be at p6 was changed to A (Italic).
T-cell clones were stimulated with B6K10 cells expressing the indicated register-fixed constructs and assayed for secreted human IFN-γ (ng/mL).