In silico B-cell and T-cell epitope-based vaccine designing against Chikungunya virus

This thesis report is submitted in partial fulfilment of the requirement for the degree of B.Sc in Microbiology, 2018.

Detalles Bibliográficos
Autor principal: Anushe, Sheikh
Otros Autores: Tabrejee, Shamira
Formato: Tesis
Lenguaje:English
Publicado: BRAC Univeristy 2018
Materias:
Acceso en línea:http://hdl.handle.net/10361/10292
id 10361-10292
record_format dspace
spelling 10361-102922019-09-30T04:52:38Z In silico B-cell and T-cell epitope-based vaccine designing against Chikungunya virus Anushe, Sheikh Tabrejee, Shamira Department of Mathematics and Natural Sciences, BRAC University Chikungunya B-cell T-cell Chikungunya vaccine CHIKV This thesis report is submitted in partial fulfilment of the requirement for the degree of B.Sc in Microbiology, 2018. Catalogued from PDF version of thesis report. Includes bibliographical references (pages 41-47). Chikungunya virus (CHIKV) is an arthropod-borne alphavirus, belonging to the Togavirus family. There is no commercial treatment or vaccine against CHIKV, despite the acute epidemics taking place in several events distributed among wide areas. In this study, we employed various computational methods to identify B-cell and T-cell epitopes from the envelope protein E1, which have the potential for vaccine development against CHIKV. By analyzing the immune parameters of the conserved sequences of E1 glycoprotein using various databases and bioinformatics tools, we identified one potential B-cell and another T-cell epitope which may be used as epitope-based peptide vaccines. Using two different B-cell epitope prediction servers, five highly similar B cell epitopes were identified from the E1 protein. Immunoinformatics analyses revealed that NTQLSEAHVEKS is a highly conserved, antigenic, surface accessible, flexible and hydrophilic B-cell epitope. Two highly conserved, non- allergenic, non-cytotoxic putative T-cell epitopes having high world population coverages were analyzed for their binding with the HLA-C 12*03 molecule. Docking simulation assay revealed that SASAKLRVL has significantly lower binding energy, which strengthened its potential as being a T-cell epitope for the epitope-based vaccine against CHIKV. This study needs more in vivo investigation. However, mindful of the stability and reproducibility of the immune system at choosing and acting against peptide epitopes, this study allows us to claim a B-cell and a T-cell epitope for the epitope-based peptide vaccine against the E1 protein of CHIKV with good confidence. Sheikh Anushe B. Science in Microbiology 2018-06-28T05:17:45Z 2018-06-28T05:17:45Z 2018 2018-05 Thesis ID 14136002 http://hdl.handle.net/10361/10292 en BRAC University theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. 47 pages application/pdf BRAC Univeristy
institution Brac University
collection Institutional Repository
language English
topic Chikungunya
B-cell
T-cell
Chikungunya vaccine
CHIKV
spellingShingle Chikungunya
B-cell
T-cell
Chikungunya vaccine
CHIKV
Anushe, Sheikh
In silico B-cell and T-cell epitope-based vaccine designing against Chikungunya virus
description This thesis report is submitted in partial fulfilment of the requirement for the degree of B.Sc in Microbiology, 2018.
author2 Tabrejee, Shamira
author_facet Tabrejee, Shamira
Anushe, Sheikh
format Thesis
author Anushe, Sheikh
author_sort Anushe, Sheikh
title In silico B-cell and T-cell epitope-based vaccine designing against Chikungunya virus
title_short In silico B-cell and T-cell epitope-based vaccine designing against Chikungunya virus
title_full In silico B-cell and T-cell epitope-based vaccine designing against Chikungunya virus
title_fullStr In silico B-cell and T-cell epitope-based vaccine designing against Chikungunya virus
title_full_unstemmed In silico B-cell and T-cell epitope-based vaccine designing against Chikungunya virus
title_sort in silico b-cell and t-cell epitope-based vaccine designing against chikungunya virus
publisher BRAC Univeristy
publishDate 2018
url http://hdl.handle.net/10361/10292
work_keys_str_mv AT anushesheikh insilicobcellandtcellepitopebasedvaccinedesigningagainstchikungunyavirus
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