A Novel Strategy for the Development of Vaccines for SARS-CoV-2 (COVID-19) and Other Viruses Using AI and Viral Shell Disorder

dc.contributor.authorGoh, Gerard Kian-Meng
dc.contributor.authorDunker, A. Keith
dc.contributor.authorFoster, James A.
dc.contributor.authorUversky, Vladimir N.
dc.contributor.departmentBiochemistry and Molecular Biology, School of Medicineen_US
dc.date.accessioned2021-11-05T18:11:39Z
dc.date.available2021-11-05T18:11:39Z
dc.date.issued2020-11-06
dc.descriptionThis article is made available for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.en_US
dc.description.abstractA model that predicts levels of coronavirus (CoV) respiratory and fecal–oral transmission potentials based on the shell disorder has been built using neural network (artificial intelligence, AI) analysis of the percentage of disorder (PID) in the nucleocapsid, N, and membrane, M, proteins of the inner and outer viral shells, respectively. Using primarily the PID of N, SARS-CoV-2 is grouped as having intermediate levels of both respiratory and fecal–oral transmission potentials. Related studies, using similar methodologies, have found strong positive correlations between virulence and inner shell disorder among numerous viruses, including Nipah, Ebola, and Dengue viruses. There is some evidence that this is also true for SARS-CoV-2 and SARS-CoV, which have N PIDs of 48% and 50%, and case-fatality rates of 0.5–5% and 10.9%, respectively. The underlying relationship between virulence and respiratory potentials has to do with the viral loads of vital organs and body fluids, respectively. Viruses can spread by respiratory means only if the viral loads in saliva and mucus exceed certain minima. Similarly, a patient is likelier to die when the viral load overwhelms vital organs. Greater disorder in inner shell proteins has been known to play important roles in the rapid replication of viruses by enhancing the efficiency pertaining to protein–protein/DNA/RNA/lipid bindings. This paper suggests a novel strategy in attenuating viruses involving comparison of disorder patterns of inner shells (N) of related viruses to identify residues and regions that could be ideal for mutation. The M protein of SARS-CoV-2 has one of the lowest M PID values (6%) in its family, and therefore, this virus has one of the hardest outer shells, which makes it resistant to antimicrobial enzymes in body fluid. While this is likely responsible for its greater contagiousness, the risks of creating an attenuated virus with a more disordered M are discussed.en_US
dc.eprint.versionFinal published versionen_US
dc.identifier.citationGoh, G. K.-M., Dunker, A. K., Foster, J. A., & Uversky, V. N. (2020). A Novel Strategy for the Development of Vaccines for SARS-CoV-2 (COVID-19) and Other Viruses Using AI and Viral Shell Disorder. Journal of Proteome Research, 19(11), 4355–4363. https://doi.org/10.1021/acs.jproteome.0c00672en_US
dc.identifier.issn1535-3893en_US
dc.identifier.urihttps://hdl.handle.net/1805/26951
dc.language.isoenen_US
dc.publisherACSen_US
dc.relation.isversionof10.1021/acs.jproteome.0c00672en_US
dc.relation.journalJournal of Proteome Researchen_US
dc.rightsPublic Health Emergencyen_US
dc.sourcePMCen_US
dc.subjectantibodyen_US
dc.subjectebolaen_US
dc.subjectCOVID-19en_US
dc.subjectnucleoproteinen_US
dc.titleA Novel Strategy for the Development of Vaccines for SARS-CoV-2 (COVID-19) and Other Viruses Using AI and Viral Shell Disorderen_US
dc.typeArticleen_US
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