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. 2020 Aug 13;5:75. doi: 10.1038/s41541-020-00224-0

Table 1.

Physiochemical properties of ChimeraT and the individual T-cell epitopes.

Protein/peptide Amino acid sequence Number of amino acids Molecular weight (kDa) Isoelectric point Instability index Aliphatic index GRAVY
ChimeraT YIMSGPARYVYFHMVLPVEAQGGRLEDQAPSTHNVEVPFVKTFTYSVLDIQPNEGGNYDPNVWCAVPNCITCDRLDPSNRGGVRVLYQPNVENLYHIYRHIGVNAETVL 109 12.31 5.40 51.03 84.77 −0.245
LiHyp1 epitope YIMSGPARYVYFHMVLPVEAQ 21 2.47 6.75 50.78 88.10 0.386
EIF5a epitope RLEDQAPSTHNVEVPFVKTFTYSVLDIQPNE 31 3.54 4.50 57.65 78.39 −0.535
LiHyp2 epitope NYDPNVWCAVPNCITCDRLDPSNR 24 2.76 4.43 39.18 60.83 −0.667
PHB epitope VRVLYQPNVENLYHIYRHIGVNAETVL 27 3.21 6.90 54.73 129.63 0.007

GRAVY grand average of hydropathy.

ChimeraT was constructed using amino acid sequences containing selected CD4+ and CD8+ T-cell epitopes from Prohibitin (PHB; Amino Acids 104–131), EIF5a (Amino Acids 71–101), LiHyp1 (Amino Acids 163–183) and LiHyp2 (Amino Acids 416–439) proteins.