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• W1978035722 startingPage "6218" @default.
• W1978035722 abstract "Flavivirus protein biosynthesis involves the proteolytic processing of a single polyprotein precursor by host- and virus-encoded proteinases. In this study, the requirement for the proteolytic function of the viral proteinase NS3 for correct processing of a polyprotein segment encompassing the Murray Valley encephalitis virus structural proteins is shown. The NS3-mediated cleavage in the structural polyprotein region presumably releases the capsid protein from its membrane anchor and triggers the appearance of the premembrane (prM) protein. This suggests that cleavage of prM by signal peptidase in the lumen of the endoplasmic reticulum is under control of a cytoplasmic cleavage catalyzed by a viral proteinase. The function of the viral proteinase is also essential for secretion of flaviviral spike proteins when expressed from cDNA via vaccinia virus recombinants or in COS cell transfections. This has important implications for the design of flavivirus subunit vaccines." @default.
• W1978035722 created "2016-06-24" @default.
• W1978035722 creator A5072894345 @default.
• W1978035722 date "1993-07-01" @default.
• W1978035722 modified "2023-10-16" @default.
• W1978035722 title "Flavivirus premembrane protein cleavage and spike heterodimer secretion require the function of the viral proteinase NS3." @default.
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• W1978035722 doi "https://doi.org/10.1073/pnas.90.13.6218" @default.
• W1978035722 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/46899" @default.
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