Targeting the SARS-CoV2 nucleocapsid protein for potential therapeutics using immuno-informatics and structure-based drug discovery techniques
The occurrence of the SARS-CoV2 infection has become a worldwide threat and the urgent need to discover therapeutic interventions remains paramount. The primary roles of the coronavirus nucleocapsid (N) protein are to interact with the viral genome and pack them into ribonucleoprotein complex. It al...
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doaj-da5abf067fd344f0b8f28e1254eed38b2021-05-21T04:18:44ZengElsevierBiomedicine & Pharmacotherapy0753-33222020-12-01132110914Targeting the SARS-CoV2 nucleocapsid protein for potential therapeutics using immuno-informatics and structure-based drug discovery techniquesAlexander Kwarteng0Ebenezer Asiedu1Samuel Amoah Sakyi2Samuel Opoku Asiedu3Department of Biochemistry and Biotechnology, Kwame Nkrumah University of Science and Technology (KNUST), Kumasi, Ghana; Kumasi Centre for Collaborative Research in Tropical Medicine (KCCR), Kumasi, Ghana; Corresponding author at: Department of Biochemistry and Biotechnology, KNUST, Kumasi, Ghana.Kumasi Centre for Collaborative Research in Tropical Medicine (KCCR), Kumasi, GhanaDepartment of Molecular Medicine, Kwame Nkrumah University of Science and Technology (KNUST), Kumasi, GhanaKumasi Centre for Collaborative Research in Tropical Medicine (KCCR), Kumasi, GhanaThe occurrence of the SARS-CoV2 infection has become a worldwide threat and the urgent need to discover therapeutic interventions remains paramount. The primary roles of the coronavirus nucleocapsid (N) protein are to interact with the viral genome and pack them into ribonucleoprotein complex. It also plays critical roles at many stages of the viral life cycle. Herein, we explore the N protein of SARS-CoV2 to identify promising epitope-based vaccine candidates and target the N-terminal domain of SARS-CoV2 N-protein for potential inhibitors using an integrative bioinformatics approach. We identified B-cell epitopes and T-cell epitopes that are non-toxic, non-allergenic, capable of inducing IFN-γ and structurally stable with high global population coverage of response. The 404SKQLQQSMSSADS416 and 92RRIRGGDGKMKDL104 sequences of N-protein were identified to induce B-cell immunity. We also identified 79SSPDDQIGY87 and 305AQFAPSASAFFGMSR319 as potential T-cell epitopes that form stable structures with human leucocyte antigens. We have also identified zidovudine triphosphate, an anti-HIV agent, as a potential inhibitor of the N-terminal domain of SARS-CoV2 N-protein based on docking and simulation analysis and should be considered for experimental validations. The findings of this study can help fast-track the discovery of therapeutic options to combat COVID-19.http://www.sciencedirect.com/science/article/pii/S0753332220311069COVID-19VaccineImmuno-informaticsEpitopeMolecular dynamics simulationZidovudine |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Alexander Kwarteng Ebenezer Asiedu Samuel Amoah Sakyi Samuel Opoku Asiedu |
spellingShingle |
Alexander Kwarteng Ebenezer Asiedu Samuel Amoah Sakyi Samuel Opoku Asiedu Targeting the SARS-CoV2 nucleocapsid protein for potential therapeutics using immuno-informatics and structure-based drug discovery techniques Biomedicine & Pharmacotherapy COVID-19 Vaccine Immuno-informatics Epitope Molecular dynamics simulation Zidovudine |
author_facet |
Alexander Kwarteng Ebenezer Asiedu Samuel Amoah Sakyi Samuel Opoku Asiedu |
author_sort |
Alexander Kwarteng |
title |
Targeting the SARS-CoV2 nucleocapsid protein for potential therapeutics using immuno-informatics and structure-based drug discovery techniques |
title_short |
Targeting the SARS-CoV2 nucleocapsid protein for potential therapeutics using immuno-informatics and structure-based drug discovery techniques |
title_full |
Targeting the SARS-CoV2 nucleocapsid protein for potential therapeutics using immuno-informatics and structure-based drug discovery techniques |
title_fullStr |
Targeting the SARS-CoV2 nucleocapsid protein for potential therapeutics using immuno-informatics and structure-based drug discovery techniques |
title_full_unstemmed |
Targeting the SARS-CoV2 nucleocapsid protein for potential therapeutics using immuno-informatics and structure-based drug discovery techniques |
title_sort |
targeting the sars-cov2 nucleocapsid protein for potential therapeutics using immuno-informatics and structure-based drug discovery techniques |
publisher |
Elsevier |
series |
Biomedicine & Pharmacotherapy |
issn |
0753-3322 |
publishDate |
2020-12-01 |
description |
The occurrence of the SARS-CoV2 infection has become a worldwide threat and the urgent need to discover therapeutic interventions remains paramount. The primary roles of the coronavirus nucleocapsid (N) protein are to interact with the viral genome and pack them into ribonucleoprotein complex. It also plays critical roles at many stages of the viral life cycle. Herein, we explore the N protein of SARS-CoV2 to identify promising epitope-based vaccine candidates and target the N-terminal domain of SARS-CoV2 N-protein for potential inhibitors using an integrative bioinformatics approach. We identified B-cell epitopes and T-cell epitopes that are non-toxic, non-allergenic, capable of inducing IFN-γ and structurally stable with high global population coverage of response. The 404SKQLQQSMSSADS416 and 92RRIRGGDGKMKDL104 sequences of N-protein were identified to induce B-cell immunity. We also identified 79SSPDDQIGY87 and 305AQFAPSASAFFGMSR319 as potential T-cell epitopes that form stable structures with human leucocyte antigens. We have also identified zidovudine triphosphate, an anti-HIV agent, as a potential inhibitor of the N-terminal domain of SARS-CoV2 N-protein based on docking and simulation analysis and should be considered for experimental validations. The findings of this study can help fast-track the discovery of therapeutic options to combat COVID-19. |
topic |
COVID-19 Vaccine Immuno-informatics Epitope Molecular dynamics simulation Zidovudine |
url |
http://www.sciencedirect.com/science/article/pii/S0753332220311069 |
work_keys_str_mv |
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