Recognition of helper T cell epitopes in envelope (E) glycoprotein of Japanese encephalitis, west Nile and Dengue viruses.

Abstract

Helper T (Th) cell antigenic sites were predicted from the primary amino acid sequence (approximately 500 in length) of the envelope (E) glycoprotein (gp) of Japanese encephalitis (JE), West Nile (WN) and Dengue (DEN) I-IV flaviviruses. Prediction of Th epitopes was done by analyzing the occurrence of amphipathic segments, Rothbard-Taylor tetra/pentamer motifs and presence of alpha helix-preferring amino acids. The simultaneous occurrence of all these parameters in segments of E gp were used as criteria for prediction as Th epitopes. Only one cross reactive epitope was predicted in the C-terminal region of the E gp predicted segments of all flaviviruses analyzed. This region is one of the longest amphipathic stretch (approximately from 420 to 455) and also has a fairly large amphipathic score. Based on the predicted findings three selected peptides were synthesized and analyzed for their ability to induce in vitro T cell proliferative response in different inbred strains of mice (Balb/c, C57BL6, C3H/HeJ). Synthetic peptide I and II prepared from C-terminal region gave a cross reactive response to JE, WN and Den-II in Balb/c and C3H/HeJ mice. Synthetic peptide III prepared from N-terminal region gave a proliferative response to DEN-II in Balb/c strain only, indicating differential antigen presentation.

• Authors: M Kutubuddin, A S Kolaskar, S Galande, M M Gore, S N Ghosh, K Banerjee
• Journal: Molecular immunology (Mol Immunol) 1991 Jan-Feb Vol. 28 Issue 1-2 Pg. 149-54 ISSN: 0161-5890 [Print] England
• PMID: 1707135 (Publication Type: Journal Article)

Chemical References

• Epitopes
• Membrane Glycoproteins
• Peptides
• Viral Envelope Proteins
• glycoprotein E, Flavivirus

Topics

• Algorithms
• Amino Acid Sequence
• Cross Reactions
• Dengue Virus (immunology)
• Encephalitis Virus, Japanese (immunology)
• Epitopes
• In Vitro Techniques
• Lymphocyte Activation
• Membrane Glycoproteins (chemistry, immunology, ultrastructure)
• Molecular Sequence Data
• Peptides (chemistry, immunology)
• Protein Conformation
• Structure-Activity Relationship
• T-Lymphocytes, Helper-Inducer (immunology)
• Viral Envelope Proteins (chemistry, immunology, ultrastructure)
• West Nile virus (immunology)