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dc.contributor.authorMalik, Yashpal S.
dc.contributor.authorKumar, Prashnat
dc.contributor.authorAnsari, Mohd Ikram
dc.contributor.authorHemida, Maged G.
dc.contributor.authorEl Zowalaty, Mohamed E.
dc.contributor.authorAbdel-Moneim, Ahmed S.
dc.contributor.authorGanesh, Balasubramanian
dc.contributor.authorSalajegheh, Sina
dc.contributor.authorNatesan, Senthilkumar
dc.contributor.authorSircar, Shubhankar
dc.contributor.authorSafdar, Muhammad
dc.contributor.authorVinodhkumar, O. R.
dc.contributor.authorDuarte, Phelipe M.
dc.contributor.authorPatel, Shailesh K.
dc.contributor.authorKlein, Jörn
dc.contributor.authorRahimi, Parastoo
dc.contributor.authorDhama, Kuldeep
dc.date.accessioned2021-09-07T10:30:38Z
dc.date.available2021-09-07T10:30:38Z
dc.date.created2021-02-18T08:35:02Z
dc.date.issued2020
dc.identifier.citationMalik, Y. S., Kumar, P., Ansari, M. I., Hemida, M. G., El Zowalaty, M. E., Abdel-Moneim, A. S., Ganesh, B., Salajegheh, S., Natesan, S., Sircar, S., Safdar, M., Vinodhkumar, O. R., Duarte, P. M., Patel, S. K., Klein, J., Rahimi, P., & Dhama, K. (2021). SARS-CoV-2 Spike Protein Extrapolation for COVID Diagnosis and Vaccine Development. Frontiers in Molecular Biosciences, 8, Artikkel 607886.en_US
dc.identifier.issn2296-889X
dc.identifier.urihttps://hdl.handle.net/11250/2773972
dc.description.abstractSevere acute respiratory syndrome coronavirus-2 (SARS-CoV-2) led to coronavirus disease 2019 (COVID-19) pandemic affecting nearly 71.2 million humans in more than 191 countries, with more than 1.6 million mortalities as of 12 December, 2020. The spike glycoprotein (S-protein), anchored onto the virus envelope, is the trimer of S-protein comprised of S1 and S2 domains which interacts with host cell receptors and facilitates virus-cell membrane fusion. The S1 domain comprises of a receptor binding domain (RBD) possessing an N-terminal domain and two subdomains (SD1 and SD2). Certain regions of S-protein of SARS-CoV-2 such as S2 domain and fragment of the RBD remain conserved despite the high selection pressure. These conserved regions of the S-protein are extrapolated as the potential target for developing molecular diagnostic techniques. Further, the S-protein acts as an antigenic target for different serological assay platforms for the diagnosis of COVID-19. Virus-specific IgM and IgG antibodies can be used to detect viral proteins in ELISA and lateral flow immunoassays. The S-protein of SARS-CoV-2 has very high sequence similarity to SARS-CoV-1, and the monoclonal antibodies (mAbs) against SARS-CoV-1 cross-react with S-protein of SARS-CoV-2 and neutralize its activity. Furthermore, in vitro studies have demonstrated that polyclonal antibodies targeted against the RBD of S-protein of SARS-CoV-1 can neutralize SARS-CoV-2 thus inhibiting its infectivity in permissive cell lines. Research on coronaviral S-proteins paves the way for the development of vaccines that may prevent SARS-CoV-2 infection and alleviate the current global coronavirus pandemic. However, specific neutralizing mAbs against SARS-CoV-2 are in clinical development. Therefore, neutralizing antibodies targeting SARS-CoV-2 S-protein are promising specific antiviral therapeutics for pre-and post-exposure prophylaxis and treatment of SARS-CoV-2 infection. We hereby review the approaches taken by researchers across the world to use spike gene and S-glycoprotein for the development of effective diagnostics, vaccines and therapeutics against SARA-CoV-2 infection the COVID-19 pandemic.en_US
dc.language.isoengen_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleSars-Cov-2 Spike Protein Extrapolation for COVID Diagnosis and Vaccine Developmenten_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.rights.holder© 2021 Malik, Kumar, Ansari, Hemida, El Zowalaty, Abdel-Moneim, Ganesh, Salajegheh, Natesan, Sircar, Safdar, Vinodhkumar, Duarte, Patel, Klein, Rahimi and Dhama.en_US
dc.source.volume8en_US
dc.source.journalFrontiers in Molecular Biosciencesen_US
dc.identifier.doihttps://doi.org/10.3389/fmolb.2021.607886
dc.identifier.cristin1891134
dc.source.articlenumber607886en_US
cristin.ispublishedfalse
cristin.fulltextpostprint
cristin.qualitycode1


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