Author: Lin Li; Ting Sun; Yufei He; Wendong Li; Yubo Fan; Jing Zhang
Title: Epitope-based peptide vaccine design and target site characterization against novel coronavirus disease caused by SARS-CoV-2 Document date: 2020_2_27
ID: e9vq3fe3_26
Snippet: Allergenicity of T-cell epitopes were assessed by Allergen FP 1.0. Results showed that two of nine MHC class-I binding peptides were probably non-allergen, and nine of thirteen MHC class-II binding peptides were predicted to be non-allergen ( Table 5 ). Toxicity of T-cell epitopes along with hydrophobicity, hydropathicity, hydrophilicity and charge were evaluated by ToxinPred. All of T-cell epitopes were predicted to be non-toxin (Table 5 ). The .....
Document: Allergenicity of T-cell epitopes were assessed by Allergen FP 1.0. Results showed that two of nine MHC class-I binding peptides were probably non-allergen, and nine of thirteen MHC class-II binding peptides were predicted to be non-allergen ( Table 5 ). Toxicity of T-cell epitopes along with hydrophobicity, hydropathicity, hydrophilicity and charge were evaluated by ToxinPred. All of T-cell epitopes were predicted to be non-toxin (Table 5 ). The stability of T-cell epitopes were evaluated through the number of peptide digesting enzymes by protein digest server. All T-cell epitopes were found to have multiple nondigesting enzymes varying from 4 to 11 enzymes ( Table 6 ).
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