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Mechanism of Antiviral Activities of Nanoviricide's Platform Technology based Biopolymer (NV-CoV-2)

NV-CoV-2 is a nanoviricide that is covalently bonded with polyethylene glycol (PEG) and alkyl pendants. This molecular design is used to attack many strains of coronaviruses in a broad-spectrum manner. The ligand works by competitive inhibition and binds to the same site on the S-protein of SARS-CoV...

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Autores principales: Chakraborty, Ashok, Diwan, Anil, Arora, Vinod, Thakur, Yogesh, Chiniga, Vijetha, Tatake, Jay, Pandey, Rajesh, Holkar, Preetam, Holkar, Neelam, Pond, Bethany
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AIMS Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9114783/
https://www.ncbi.nlm.nih.gov/pubmed/35634020
http://dx.doi.org/10.3934/publichealth.2022028
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author Chakraborty, Ashok
Diwan, Anil
Arora, Vinod
Thakur, Yogesh
Chiniga, Vijetha
Tatake, Jay
Pandey, Rajesh
Holkar, Preetam
Holkar, Neelam
Pond, Bethany
author_facet Chakraborty, Ashok
Diwan, Anil
Arora, Vinod
Thakur, Yogesh
Chiniga, Vijetha
Tatake, Jay
Pandey, Rajesh
Holkar, Preetam
Holkar, Neelam
Pond, Bethany
author_sort Chakraborty, Ashok
collection PubMed
description NV-CoV-2 is a nanoviricide that is covalently bonded with polyethylene glycol (PEG) and alkyl pendants. This molecular design is used to attack many strains of coronaviruses in a broad-spectrum manner. The ligand works by competitive inhibition and binds to the same site on the S-protein of SARS-CoV that attaches to the cognate cellular receptor, ACE2. This prevents SARS-CoV from binding and infecting the cell. NV-CoV-2 is designed to bind to the free virion particles at multiple points encapsulate the virus and disable its ability to infect the cells. The multi-point binding interaction, like a nano-velcro-tape, may lead to lipid-lipid fusion of the alkyl chains in the nanoviricide micelle with the lipid envelope of the virus. The virus becomes dismantled to a capsid form before the host immune system becomes involved. This putative mechanism is orthogonal to many other anti-coronavirus agents in development. Thus, it maybe possible to produce a stronger antiviral effect when combining NV-CoV-2 therapy with other anti-coronavirus therapies such as Remdesivir (RDV). NV-CoV-2 can encapsulate other antiviral compounds as well. In this study, RDV was encapsulated and protected from serum-mediated degradation in vivo. As a result, RDV was available for a longer period of time to interact with RNA polymerase and inhibit.
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spelling pubmed-91147832022-05-27 Mechanism of Antiviral Activities of Nanoviricide's Platform Technology based Biopolymer (NV-CoV-2) Chakraborty, Ashok Diwan, Anil Arora, Vinod Thakur, Yogesh Chiniga, Vijetha Tatake, Jay Pandey, Rajesh Holkar, Preetam Holkar, Neelam Pond, Bethany AIMS Public Health Review NV-CoV-2 is a nanoviricide that is covalently bonded with polyethylene glycol (PEG) and alkyl pendants. This molecular design is used to attack many strains of coronaviruses in a broad-spectrum manner. The ligand works by competitive inhibition and binds to the same site on the S-protein of SARS-CoV that attaches to the cognate cellular receptor, ACE2. This prevents SARS-CoV from binding and infecting the cell. NV-CoV-2 is designed to bind to the free virion particles at multiple points encapsulate the virus and disable its ability to infect the cells. The multi-point binding interaction, like a nano-velcro-tape, may lead to lipid-lipid fusion of the alkyl chains in the nanoviricide micelle with the lipid envelope of the virus. The virus becomes dismantled to a capsid form before the host immune system becomes involved. This putative mechanism is orthogonal to many other anti-coronavirus agents in development. Thus, it maybe possible to produce a stronger antiviral effect when combining NV-CoV-2 therapy with other anti-coronavirus therapies such as Remdesivir (RDV). NV-CoV-2 can encapsulate other antiviral compounds as well. In this study, RDV was encapsulated and protected from serum-mediated degradation in vivo. As a result, RDV was available for a longer period of time to interact with RNA polymerase and inhibit. AIMS Press 2022-04-12 /pmc/articles/PMC9114783/ /pubmed/35634020 http://dx.doi.org/10.3934/publichealth.2022028 Text en © 2022 the Author(s), licensee AIMS Press https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0 (https://creativecommons.org/licenses/by/4.0/) )
spellingShingle Review
Chakraborty, Ashok
Diwan, Anil
Arora, Vinod
Thakur, Yogesh
Chiniga, Vijetha
Tatake, Jay
Pandey, Rajesh
Holkar, Preetam
Holkar, Neelam
Pond, Bethany
Mechanism of Antiviral Activities of Nanoviricide's Platform Technology based Biopolymer (NV-CoV-2)
title Mechanism of Antiviral Activities of Nanoviricide's Platform Technology based Biopolymer (NV-CoV-2)
title_full Mechanism of Antiviral Activities of Nanoviricide's Platform Technology based Biopolymer (NV-CoV-2)
title_fullStr Mechanism of Antiviral Activities of Nanoviricide's Platform Technology based Biopolymer (NV-CoV-2)
title_full_unstemmed Mechanism of Antiviral Activities of Nanoviricide's Platform Technology based Biopolymer (NV-CoV-2)
title_short Mechanism of Antiviral Activities of Nanoviricide's Platform Technology based Biopolymer (NV-CoV-2)
title_sort mechanism of antiviral activities of nanoviricide's platform technology based biopolymer (nv-cov-2)
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9114783/
https://www.ncbi.nlm.nih.gov/pubmed/35634020
http://dx.doi.org/10.3934/publichealth.2022028
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