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OJBTM
Online
Journal of Bioinformatics©
Established 1995
ISSN 1443-2250
Volume 21(3): 225-235, 2020.
In Silico prediction of putative epitopes in structural polyprotein of Chikungunya virus
J. Asnet Mary1 (MSc,
ADBI), S. Kavitha1 (MSc), V. Victoria1(MSc),
R. Paramasivan2 (PhD), R.Shenbagarathai1(PhD)*,
P. Selvanayagam1 (PhD), T. Madhanmohan3
(PhD).
1. Bioinformatics Centre, Department of Biotechnology, Lady Doak College, 2. CRME (ICMR), Madurai 3. Department of Biotechnology, New Delhi, India.
Asnet Mary J, Kavitha S, Victoria V, Paramasivan
R, Shenbagarathai R, Selvanayagam
P, Madhanmohan T., In Silico prediction of putative epitopes in structural
polyprotein of Chikungunya virus, Onl J Bioinform., 21(3): 225-235,
2020. Chikungunya (CHIKF)
is associated with acute fever, including asthenia, skin rash, polyarthritis
and occasionally, encephalitis in humans. The virus is transmitted by Aedes aegypti and Aedes albopictus and there is no specific treatment or vaccine
as of this date. We predict putative epitopes of Chikungunya virus from In silico analysis of genome sequences
with Open reading frame (ORF) and putative proteins by BLAST. 3D structure of
viral polyproteins and 17 B-cell epitopes were determined for accessibility, flexibility, hydrophilicity,
β-turn
and linearity by BCPred server. One epitope capsid
protein with residues range 85 – 104 amino acid was immunogenic in the entire structural polyprotein
of CHIKV in BCIPED database with maximum score. We
used PROPREDL to test B-cell epitope for T-cell epitopes and MHC class I
binding sites. We found binding with 25 MHC alleles in humans supporting
further assessment of these putative epitopes of CHIKV In Vivo.
Keywords: Chikungunya virus, genome, epitopes, BCPred, Bcipep, MHC binding, vaccine.
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