DESAIN VAKSIN MULTI-EPITOPE MYCOBACTERIUM TUBERCULOSIS MELALUI PENDEKATAN REVERSE VACCINOLOGY

Mycobacterium tuberculosis (Mtb) is responsible for thousands of mortality in Indonesia annually. On the other hand, BCG remains the only commercial vaccine for tuberculosis (TB), with different efficacies (0-80%) towards adults. Therefore, an alternative vaccine is currently necessary. This rese...

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Main Author: Nur Ainina, Fadia
Format: Final Project
Language:Indonesia
Online Access:https://digilib.itb.ac.id/gdl/view/57933
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Institution: Institut Teknologi Bandung
Language: Indonesia
id id-itb.:57933
spelling id-itb.:579332021-08-27T17:45:13ZDESAIN VAKSIN MULTI-EPITOPE MYCOBACTERIUM TUBERCULOSIS MELALUI PENDEKATAN REVERSE VACCINOLOGY Nur Ainina, Fadia Indonesia Final Project Immune system, in silico, molecular docking, MmpL, Mtb. INSTITUT TEKNOLOGI BANDUNG https://digilib.itb.ac.id/gdl/view/57933 Mycobacterium tuberculosis (Mtb) is responsible for thousands of mortality in Indonesia annually. On the other hand, BCG remains the only commercial vaccine for tuberculosis (TB), with different efficacies (0-80%) towards adults. Therefore, an alternative vaccine is currently necessary. This research objective is to construct a multi-epitope-based vaccine that is protective towards the Indonesian population using MmpL as the antigen through a reverse vaccinology approach. The research method starts with MmpL protein sequences retrieval, whose epitopes will be predicted and selected using several parameters, including toxicity and allergenicity. Then, CTL and HTL epitopes predictions are conducted based on Indonesian population-specific HLA. Next, we performed the population coverage analysis, the physicochemical characteristics, structural analysis of the vaccine, and molecular docking. Finally, we did the codon optimization and in silico cloning in the plasmid pET28a(+). We found eight epitopes, covering 85.15% Indonesian population, with a Z-score of -4.98, and the significant residues of TLR4 such as Arg382 and Arg447, interact with the epitope. The Gibbs free energy from the docking result is - 9.1 kcal/mol, meaning that these bonds could be spontaneously formed energetically. Hopefully, the vaccine candidate can protect the Indonesian population and induce cellular, humoral, and cascade immune response from TLR4 against Mtb. Furthermore, the efficacy of the vaccine in inducing immune response will be investigated through wet-lab research. text
institution Institut Teknologi Bandung
building Institut Teknologi Bandung Library
continent Asia
country Indonesia
Indonesia
content_provider Institut Teknologi Bandung
collection Digital ITB
language Indonesia
description Mycobacterium tuberculosis (Mtb) is responsible for thousands of mortality in Indonesia annually. On the other hand, BCG remains the only commercial vaccine for tuberculosis (TB), with different efficacies (0-80%) towards adults. Therefore, an alternative vaccine is currently necessary. This research objective is to construct a multi-epitope-based vaccine that is protective towards the Indonesian population using MmpL as the antigen through a reverse vaccinology approach. The research method starts with MmpL protein sequences retrieval, whose epitopes will be predicted and selected using several parameters, including toxicity and allergenicity. Then, CTL and HTL epitopes predictions are conducted based on Indonesian population-specific HLA. Next, we performed the population coverage analysis, the physicochemical characteristics, structural analysis of the vaccine, and molecular docking. Finally, we did the codon optimization and in silico cloning in the plasmid pET28a(+). We found eight epitopes, covering 85.15% Indonesian population, with a Z-score of -4.98, and the significant residues of TLR4 such as Arg382 and Arg447, interact with the epitope. The Gibbs free energy from the docking result is - 9.1 kcal/mol, meaning that these bonds could be spontaneously formed energetically. Hopefully, the vaccine candidate can protect the Indonesian population and induce cellular, humoral, and cascade immune response from TLR4 against Mtb. Furthermore, the efficacy of the vaccine in inducing immune response will be investigated through wet-lab research.
format Final Project
author Nur Ainina, Fadia
spellingShingle Nur Ainina, Fadia
DESAIN VAKSIN MULTI-EPITOPE MYCOBACTERIUM TUBERCULOSIS MELALUI PENDEKATAN REVERSE VACCINOLOGY
author_facet Nur Ainina, Fadia
author_sort Nur Ainina, Fadia
title DESAIN VAKSIN MULTI-EPITOPE MYCOBACTERIUM TUBERCULOSIS MELALUI PENDEKATAN REVERSE VACCINOLOGY
title_short DESAIN VAKSIN MULTI-EPITOPE MYCOBACTERIUM TUBERCULOSIS MELALUI PENDEKATAN REVERSE VACCINOLOGY
title_full DESAIN VAKSIN MULTI-EPITOPE MYCOBACTERIUM TUBERCULOSIS MELALUI PENDEKATAN REVERSE VACCINOLOGY
title_fullStr DESAIN VAKSIN MULTI-EPITOPE MYCOBACTERIUM TUBERCULOSIS MELALUI PENDEKATAN REVERSE VACCINOLOGY
title_full_unstemmed DESAIN VAKSIN MULTI-EPITOPE MYCOBACTERIUM TUBERCULOSIS MELALUI PENDEKATAN REVERSE VACCINOLOGY
title_sort desain vaksin multi-epitope mycobacterium tuberculosis melalui pendekatan reverse vaccinology
url https://digilib.itb.ac.id/gdl/view/57933
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