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Chasing COVID-19 through SARS-CoV-2 spike glycoprotein

An ongoing pandemic Coronavirus disease (COVID-19), caused by a newly emerged Coronavirus, SARS-CoV-2 has affected millions of people globally. One of the most crucial structural proteins of SARS-CoV-2 is the Spike glycoprotein (S-glycoprotein), for which the first de novo modelling was envisaged by...

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Autores principales: Saxena, Shailendra K., Kumar, Swatantra, Baxi, Preeti, Srivastava, Nishant, Puri, Bipin, Ratho, R. K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer India 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7718591/
https://www.ncbi.nlm.nih.gov/pubmed/33313362
http://dx.doi.org/10.1007/s13337-020-00642-7
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author Saxena, Shailendra K.
Kumar, Swatantra
Baxi, Preeti
Srivastava, Nishant
Puri, Bipin
Ratho, R. K.
author_facet Saxena, Shailendra K.
Kumar, Swatantra
Baxi, Preeti
Srivastava, Nishant
Puri, Bipin
Ratho, R. K.
author_sort Saxena, Shailendra K.
collection PubMed
description An ongoing pandemic Coronavirus disease (COVID-19), caused by a newly emerged Coronavirus, SARS-CoV-2 has affected millions of people globally. One of the most crucial structural proteins of SARS-CoV-2 is the Spike glycoprotein (S-glycoprotein), for which the first de novo modelling was envisaged by our group in early 2020, and was superimposed to its predecessor SARS-CoV S-glycoprotein, to determine structural divergence, glycosylation and antigenic variation between SARS-CoV-2 and SARS-CoV. S-glycoprotein is involved in binding with the cellular receptor, membrane fusion, internalization via angiotensin-converting enzyme 2 (ACE2) receptor, and tissue tropism. Upon internalization into the target host cells, the viral genome encodes two precursor polypeptides which get processed into 16 mature nonstructural proteins that play a crucial role in replication and transcription of SARS-CoV-2. Currently S-glycoprotein is one of the most vital targets for vaccine and therapeutics development for COVID-19.
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spelling pubmed-77185912020-12-07 Chasing COVID-19 through SARS-CoV-2 spike glycoprotein Saxena, Shailendra K. Kumar, Swatantra Baxi, Preeti Srivastava, Nishant Puri, Bipin Ratho, R. K. Virusdisease Editorial An ongoing pandemic Coronavirus disease (COVID-19), caused by a newly emerged Coronavirus, SARS-CoV-2 has affected millions of people globally. One of the most crucial structural proteins of SARS-CoV-2 is the Spike glycoprotein (S-glycoprotein), for which the first de novo modelling was envisaged by our group in early 2020, and was superimposed to its predecessor SARS-CoV S-glycoprotein, to determine structural divergence, glycosylation and antigenic variation between SARS-CoV-2 and SARS-CoV. S-glycoprotein is involved in binding with the cellular receptor, membrane fusion, internalization via angiotensin-converting enzyme 2 (ACE2) receptor, and tissue tropism. Upon internalization into the target host cells, the viral genome encodes two precursor polypeptides which get processed into 16 mature nonstructural proteins that play a crucial role in replication and transcription of SARS-CoV-2. Currently S-glycoprotein is one of the most vital targets for vaccine and therapeutics development for COVID-19. Springer India 2020-12-05 2020-12 /pmc/articles/PMC7718591/ /pubmed/33313362 http://dx.doi.org/10.1007/s13337-020-00642-7 Text en © Indian Virological Society 2020
spellingShingle Editorial
Saxena, Shailendra K.
Kumar, Swatantra
Baxi, Preeti
Srivastava, Nishant
Puri, Bipin
Ratho, R. K.
Chasing COVID-19 through SARS-CoV-2 spike glycoprotein
title Chasing COVID-19 through SARS-CoV-2 spike glycoprotein
title_full Chasing COVID-19 through SARS-CoV-2 spike glycoprotein
title_fullStr Chasing COVID-19 through SARS-CoV-2 spike glycoprotein
title_full_unstemmed Chasing COVID-19 through SARS-CoV-2 spike glycoprotein
title_short Chasing COVID-19 through SARS-CoV-2 spike glycoprotein
title_sort chasing covid-19 through sars-cov-2 spike glycoprotein
topic Editorial
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7718591/
https://www.ncbi.nlm.nih.gov/pubmed/33313362
http://dx.doi.org/10.1007/s13337-020-00642-7
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