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Table 1.

Candidate peptides derived from SCRN1 and their predicted binding affinities to HLA‐A*0201

Position † Sequence ‡ (9‐mer) Score § Position † Sequence ‡ (10‐mer) Score §
303 SIFKPFIFV 369.7 308 FIFVDDVKLV 374.3
 75 WLWGAEMGA 189.6 158 LIVDRDEAWV 366.6
 68 IMISRPAWL 144.2 272 FLTTASGVSV 319.9
107 LLGMDLVRL  83.5 371 TMLEIEKQGL 234.0
308 FIFVDDVKL  49.9 106 ALLGMDLVRL 181.7
265 VCIDSEFFL  31.0 (N.S.)  67 AIMISRPAWL  59.7
306 KPFIFVDDV  25.1 (N.S.) 264 GVCIDSEFFL  59.6
159 IVDRDEAWV  22.7 315 KLVPKTQSPC  17.3
257 TLRDKASGV  21.6 220 FNFSEVFSPV  14.6
196 KMDAEHPEL  21.6  56 YISIDQVPRT  10.8
126 ALDVIVSLL  19.6 216 GEGEFNFSEV  10.5
207 YAQSQGWWT  19.6 (N.S.) 175 WAAEKVTEGV   8.9
367 KLRSTMLEL  13.0 281 VLPQNRSSPC   8.4
157 YLIVDRDEA  11.1   2 AAAPPSYCFV   7.9
  3 AAPPSYCFV   7.9 253 TMMNTLRDKA   6.5
109 GMDLVRLGL   6.1 397 EVGDIFYDCV   5.2
179 KVTEGVRCI   6.0  79 AEMGANEHGV   5.0
266 CIDSEFFLT   4.5  20 GLVVFGKNSA   4.9
250 TVQTMMNTL   4.2 190 QLSLTTKMDA   4.9 (N.S.)
 80 EMGANEHGV   3.7 302 RSIFKPFIFV   4.7

The amino acid sequences of candidate peptides are listed in the order of binding affinities to HLA‐A*0201 molecules.

†

The amino acid sequence number for position 1 in the candidate peptide, counting from the N‐terminal of SCRN1;

‡

‡ The standard single letter amino acid code is used.

§

§ The estimated half‐life of dissociation score for each peptide was calculated using BIMAS software. Higher scores indicate higher affinity to MHC class I molecules. N.S., not synthesized due to the high hydrophobicity of amino acid sequences.