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• W3100520004 startingPage "104282" @default.
• W3100520004 abstract "Severe acute respiratory syndrome-coronavirus (SARS-CoV)-2 is a newly emerging type of CoV. We evaluated the predicted anti-SARS-CoV-2 effect of major royal jelly protein (MRJP)2 and MRJP2 isoform X1, which recently showed high efficacy against other enveloped RNA-viruses (HCV and HIV). Some in-silico analyses have been performed to predict the impact of these proteins on viral entry, replication, and complications. These proteins have shown a high potency in sialic acid hydrolysis from the lung cells (WI-38) surface. Docking analysis showed that these proteins have a high binding affinity to viral receptor-binding sites in the receptor-binding domain, causing attachment prevention. Moreover, MRJPs can exert an inhibitory influence, via different mechanisms, for SARS-CoV-2 non-structural proteins (main and papain proteases, RNA replicase, RNA-dependent RNA polymerase, and methyltransferase). Also, they can bind to hemoglobin-binding sites on viral-nsps and prevent their hemoglobin attack. Thus, MRJP2 and MRJP2 X1 can be a promising therapy for SARS-CoV-2 infection." @default.
• W3100520004 created "2020-11-23" @default.
• W3100520004 creator A5054611309 @default.
• W3100520004 creator A5069557540 @default.
• W3100520004 date "2020-12-01" @default.
• W3100520004 modified "2023-10-16" @default.
• W3100520004 title "The potential antiviral effect of major royal jelly protein2 and its isoform X1 against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2): Insight on their sialidase activity and molecular docking" @default.
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• W3100520004 doi "https://doi.org/10.1016/j.jff.2020.104282" @default.
• W3100520004 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/7656998" @default.
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