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Control of baculovirus gp64-induced syncytium formation by membrane lipid composition.
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2
Baculovirus gp64 envelope glycoprotein is sufficient to mediate pH-dependent membrane fusion.
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Incorporation of GP64 into Helicoverpa armigera nucleopolyhedrovirus enhances virus infectivity in vivo and in vitro.
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Non-bilayer lipids and biological fusion intermediates.
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Unraveling the entry mechanism of baculoviruses and its evolutionary implications.
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Envelope-Fusion-Syncytium Formation in Maturation.
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The late endosome-resident lipid bis(monoacylglycero)phosphate is a cofactor for Lassa virus fusion.
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SARS-CoV fusion peptides induce membrane surface ordering and curvature.
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Maturation of the Gag core decreases the stability of retroviral lipid membranes.
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Baculovirus GP64-mediated entry into mammalian cells.
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Intracellular curvature-generating proteins in cell-to-cell fusion.
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3
A spring-loaded mechanism for the conformational change of influenza hemagglutinin.
Cell. 1993 May 21;73(4):823-32. doi: 10.1016/0092-8674(93)90260-w.
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Lysolipids reversibly inhibit Ca(2+)-, GTP- and pH-dependent fusion of biological membranes.
FEBS Lett. 1993 Feb 22;318(1):71-6. doi: 10.1016/0014-5793(93)81330-3.
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Mechanisms of membrane fusion.
Annu Rev Biophys Biomol Struct. 1993;22:433-66. doi: 10.1146/annurev.bb.22.060193.002245.
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Lipid-anchored influenza hemagglutinin promotes hemifusion, not complete fusion.
Cell. 1994 Jan 28;76(2):383-91. doi: 10.1016/0092-8674(94)90344-1.

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