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. 2010 May 7;5(5):e10533. doi: 10.1371/journal.pone.0010533

Table 6. Affinities of peptides to MHC-II alleles.

Peptide sequence DRB1*0101 DRB1*0301 DRB1*0302 DRB1*0401 DRB3*0301 DRB5*0101 DPA1*0103/DPB1*0401
HA306–318 YKYVKQNTLKLAT 108 a 26 53 15 3 12 NB
hypothetical protein 239–253 [27] YILLKKILSSRFNQM 435 20 156 107 3 17 25
DR/Donor 1 b IMLKANFSV (PF-103) 3433 c NB NB 1387 18 NB NB c
DR/Donor 25 ETIVLLRAF (PF-113) 3729 NB c NB NB NB 780 c NB
DP/Donor 23 LVSLGAISF (PF-148) 4340 c NBc NB NB NB NB NB c
DR/Donor 32 YVKQNTLKL (PF-152) 1203 NB 2221 226 c 356 405 NB c
DP/Donor 23 IAPWYAFAL (PF-154) NB c NB c NB NB NB 1696 NB c
Donor 17 d LMNELGVPF (PF-141) NB NB NB NB 4014 NB NB
DP/Donor 23 LPFHNVHPL (PF-147) NB c NB c NB NB NB 3704 NB c
DP/Donor 31 LPFQNVHPV (PF-150) NB NB NB NB NB 1204 c NB c

Note: peptides marked in bold are positive controls included in the assay; HA306–318 is a promiscuous HLA-DR binder whereas hypothetical protein 239–253 has been shown to bind most HLA-DR alleles and the HLA-DP allele. Peptide showing affinities above 5000 nM are categorized as non-binders (NB).

a

Peptide binding affinity (KD) in nM.

b

Peptide reactivity blocked by anti-HLA-II subtype antibody in the responding donor number (See Fig. 2 and Table 5).

c

The HLA-II subtype assayed for peptide binding was expressed by donor.

d

No cells available for HLA-II typing.