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. 2012 Apr 10;7(4):e34627. doi: 10.1371/journal.pone.0034627

Table 2. Characteristics of peptide fragments used for human IgE-binding dot-blot assays.

Peptide No. IgE reactivity (%) N-terminal sequence Mass (Da) [M+H]+ Position in Pen c 13
S1 10 ANVVQ 2013.0 Ala1-Lys19
S2 TGTTS 1008.4 Thr21-Asp29
S3 TYDST 1336.5 Thr27-Tyr39
S4 70 STAGE 2154.0 Ser30-Asp51
S5 10 GVDTG 1362.6 Gly40-Phe52
S6 FGGRA 1406.4 Phe52-Asp64
S7 10 WGTNV 2814.0 Trp58-Lys85
S8 10 YGVAK 537.4 Tyr86-Lys90
S9 KATLV 829.0 Lys91-Lys98
S10 60 VAVKV 2220 Val95-Trp117
S11 50 VLGAD 2121 Val99-Lys120
S12 20 AKSRG 1970 Ala122-Glu140
S13 YVMNM 1462.0 Tyr131-Lys143
S14 SKAVN 1691.0 Ser142-Phe158
S15 AVNDA 1071.0 Ala144-Lys154
S16 90 AAANV 1818.0 Ala148-Glu166
S17 NASNS 1105.1 Asn169-Glu180
S18 50 VCTIA 2442.0 Val181-Asp204
S19 60 TNFGS 2771.0 Thr197-Leu224
S20 SGTSM 1489.0 Ser225-Tyr240
S21 AAPHV 1222.2 Ala230-Met242
S22 100 ALEGV 3438.0 Ala243-Lys274
S23 IVQLA 1174.0 Ile256-Arg266
S24 LLYNG 905.5 Leu275-Val282

The purity of the peptides was assessed by N-terminal sequencing.

N-terminal residues were determined by Edman degradation.

Mass was determined using a QSTAR XL mass spectrometer.