Table 2.

Binding affinity and HLA/peptide complex stability of CYP1B1-derived and control peptides to human HLA-A*0201






T2 assay

Peptide
Protein
Position
Sequence
Maximum, FI*
t1/2, h
IC50, nmol
CYP190 CYP1B1 190 FLDPRPLTV 3.7 10.1 67 
CYP239   CYP1B1   239   SLVDVMPWL   3.9   3.3   63  
Controls       
    Positive MAGE-3 271 FLWGPRALV 3.2 3.4 ND 
    Negative
 
Idiotype
 
98
 
AHTKDGFNF
 
0
 
ND
 
ND
 





T2 assay

Peptide
Protein
Position
Sequence
Maximum, FI*
t1/2, h
IC50, nmol
CYP190 CYP1B1 190 FLDPRPLTV 3.7 10.1 67 
CYP239   CYP1B1   239   SLVDVMPWL   3.9   3.3   63  
Controls       
    Positive MAGE-3 271 FLWGPRALV 3.2 3.4 ND 
    Negative
 
Idiotype
 
98
 
AHTKDGFNF
 
0
 
ND
 
ND
 

FI indicates mean fluorescence with peptide/mean fluorescence without peptide; ND, not determined.

*

The known HLA-A*0201-binding peptide from MAGE-3 and a nonbinding peptide from an idiotype sequence were used as positive and negative controls. Results from 1 of 5 representative experiments are shown.

Time to half-maximal FI after withdrawal of peptide was calculated using linear regression analysis.

Peptide concentration necessary to inhibit binding of a labeled reference peptide HBV core 18-27 to HLA-A*0201 by 50%.

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