Journal of Virology · 2000 · 209 citations · 32 references
Life SciencesBiochemistryMicrobiologyMolecular VirologyProtein FoldingVirologyProtein Folding PathwaysViral AssemblyViral MaturationViral Protein ProcessingViral StructureVirus StructureViral Envelope GlycoproteinsViral Envelope Protein ProcessingViral Envelope ProteinsViral Glycoprotein ProcessingViral GlycoproteinsViral Protein FoldingViral Protein Processing In The Endoplasmic ReticulumVirion Morphogenesis
We report that endoplasmic reticulum alpha-glucosidase inhibitors have antiviral effects on dengue (DEN) virus. We found that glucosidase inhibition strongly affects productive folding pathways of the envelope glycoproteins prM (the intracellular glycosylated precursor of M [membrane protein]) and E (envelope protein): the proper folding of prM bearing unprocessed N-linked oligosaccharide is inefficient, and this causes delayed formation of prME heterodimer. The complexes formed between incompletely folded prM and E appear to be unstable, leading to a nonproductive pathway. Inhibition of alpha-glucosidase-mediated N-linked oligosaccharide trimming may thus prevent the assembly of DEN virus by affecting the early stages of envelope glycoprotein processing.
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