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. 2013 Nov 5;8(11):e78389. doi: 10.1371/journal.pone.0078389

Table 1. HLA-A2-binding capability of the predicted EGFR T790M-derived peptides.

Peptide name Amino acid sequence NetMHC 3.2 ANN IC50 (nM) BIMAS score HLA-binding capability (%)a
T790M-1 VQLIMQLMPF 3705 0.109 0
T790M-2 QLIMQLMPFG 4054 0.943 0
T790M-3 LIMQLMPFGC 837 24.921 0
T790M-4 IMQLMPFGCL 925 6.478 0
T790M-5 MQLMPFGCLL 977 51.770 207.5
T790M-6 LTSTVQLIMQL 4187 NAc 0
T790M-7 LIMQLMPFGCL 530 NA 19.1
T790M-8 IMQLMPFGCLL 118 NA 57.0
WT-5b TQLMPFGCLL 2578 30.453 158.2
WT-7b LITQLMPFGCL 5063 NA 0
Flu-M1 GILGFVFTL 18 550.927 234.4
a

HLA-A2-binding capability was estimated by the increase in mean fluorescence intensity (MFI) as determined by flow cytometry after staining of RMA-S/A2 cells with anti-HLA-A2 mAb, as follows: MFI increase (%)  =  (MFI with a given peptide – MFI without peptides)/(MFI without peptides) X 100. The experiments were repeated three times and a representative result is shown.

b

WT-5 and WT-7 peptides have wild-type sequences, corresponding to the T790M-5 and T790M-7 peptides, respectively.

c

NA, not available.