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• W3164273635 endingPage "e0251426" @default.
• W3164273635 startingPage "e0251426" @default.
• W3164273635 abstract "Two SARS-CoV-2 variants of concern showing increased transmissibility relative to the Wuhan virus have recently been identified. Although neither variant appears to cause more severe illness nor increased risk of death, the faster spread of the virus is a major threat. Using computational tools, we found that the new SARS-CoV-2 variants may acquire an increased transmissibility by increasing the propensity of its spike protein to expose the receptor binding domain via proteolysis, perhaps by neutrophil elastase and/or via reduced intramolecular interactions that contribute to the stability of the closed conformation of spike protein. This information leads to the identification of potential treatments to avert the imminent threat of these more transmittable SARS-CoV-2 variants." @default.
• W3164273635 created "2021-06-07" @default.
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• W3164273635 date "2021-05-26" @default.
• W3164273635 modified "2023-09-27" @default.
• W3164273635 title "Increased elastase sensitivity and decreased intramolecular interactions in the more transmissible 501Y.V1 and 501Y.V2 SARS-CoV-2 variants’ spike protein–an in silico analysis" @default.
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• W3164273635 doi "https://doi.org/10.1371/journal.pone.0251426" @default.
• W3164273635 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/8153447" @default.
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• W3164273635 hasPublicationYear "2021" @default.
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