Unknown

Dataset Information

0

Physico-chemical requirements and kinetics of membrane fusion of flavivirus-like particles.


ABSTRACT: Flaviviruses deliver their RNA genome into the host-cell cytoplasm by fusing their lipid envelope with a cellular membrane. Expression of the flavivirus pre-membrane and envelope glycoprotein genes in the absence of other viral genes results in the spontaneous assembly and secretion of virus-like particles (VLPs) with membrane fusion activity. Here, we examined the physico-chemical requirements for membrane fusion of VLPs from West Nile and Japanese encephalitis viruses. In a bulk fusion assay, optimal hemifusion (or lipid mixing) efficiencies were observed at 37 °C. Fusion efficiency increased with decreasing pH; half-maximal hemifusion was attained at pH 5.6. The anionic lipids bis(monoacylglycero)phosphate and phosphatidylinositol-3-phosphate, when present in the target membrane, significantly enhanced fusion efficiency, consistent with the emerging model that flaviviruses fuse with intermediate-to-late endosomal compartments, where these lipids are most abundant. In a single-particle fusion assay, VLPs catalysed membrane hemifusion, tracked as lipid mixing with the cellular membrane, on a timescale of 7-20 s after acidification. Lipid mixing kinetics suggest that hemifusion is a kinetically complex, multistep process.

SUBMITTER: Esposito DL 

PROVIDER: S-EPMC4635454 | biostudies-literature | 2015 Jul

REPOSITORIES: biostudies-literature

altmetric image

Publications

Physico-chemical requirements and kinetics of membrane fusion of flavivirus-like particles.

Espósito Danillo L A DL   Nguyen Jennifer B JB   DeWitt David C DC   Rhoades Elizabeth E   Modis Yorgo Y  

The Journal of general virology 20150304 Pt 7


Flaviviruses deliver their RNA genome into the host-cell cytoplasm by fusing their lipid envelope with a cellular membrane. Expression of the flavivirus pre-membrane and envelope glycoprotein genes in the absence of other viral genes results in the spontaneous assembly and secretion of virus-like particles (VLPs) with membrane fusion activity. Here, we examined the physico-chemical requirements for membrane fusion of VLPs from West Nile and Japanese encephalitis viruses. In a bulk fusion assay,  ...[more]

Similar Datasets

| S-EPMC4293572 | biostudies-literature
| S-EPMC1797619 | biostudies-literature
| S-EPMC3477123 | biostudies-literature
| S-EPMC3165785 | biostudies-literature
| S-EPMC3126228 | biostudies-literature
| S-EPMC2568029 | biostudies-literature
| S-EPMC2556630 | biostudies-literature
| S-EPMC9239988 | biostudies-literature
| S-EPMC156766 | biostudies-literature