Evidence that Rabies Virus Forms Different Kinds of Fusion Machines with Different pH Thresholds for Fusion
- 15 August 2004
- journal article
- Published by American Society for Microbiology in Journal of Virology
- Vol. 78 (16) , 8746-52
- https://doi.org/10.1128/jvi.78.16.8746-8752.2004
Abstract
Fusion of rabies virus with membranes is triggered at a low pH and is mediated by a viral glycoprotein (G). Fusion of rabies virus with liposomes was monitored by using a lipid mixing assay based on fluorescence resonance energy transfer. Fusion was detected below pH 6.4, and its extent increased with H(+) concentrations to be maximal around pH 6.15. The origin of the partial fusion activity of rabies virus under suboptimal pH conditions (i.e., between pH 6.15 and 6.4) was investigated. We demonstrate unambiguously that fusion at a suboptimal pH is distinct from the phenomenon of low-pH-induced inactivation and that it is not due to heterogeneity of the virus population. We also show that viruses that do not fuse under suboptimal pH conditions are indeed bound to the target liposomes and that the fusion complexes they have formed are blocked at an early stage of the fusion pathway. Our conclusion is that along the fusion reaction, different kinds of fusion machines with different pH thresholds for fusion can be formed. Possible explanations of this difference of pH sensitivity are discussed.Keywords
This publication has 41 references indexed in Scilit:
- Kinetically Differentiating Influenza Hemagglutinin Fusion and Hemifusion MachinesBiophysical Journal, 2003
- Evidence That the Transition of HIV-1 Gp41 into a Six-Helix Bundle, Not the Bundle Configuration, Induces Membrane FusionThe Journal of cell biology, 2000
- Receptor Binding and Membrane Fusion in Virus Entry: The Influenza HemagglutininAnnual Review of Biochemistry, 2000
- An Early Stage of Membrane Fusion Mediated by the Low pH Conformation of Influenza Hemagglutinin Depends upon Membrane LipidsThe Journal of cell biology, 1997
- The initial fusion pore induced by baculovirus GP64 is large and forms quickly.The Journal of cell biology, 1996
- Dilation of the influenza hemagglutinin fusion pore revealed by the kinetics of individual cell-cell fusion events.The Journal of cell biology, 1996
- Partial Fusion Activity of Influenza Virus toward Liposomes and Erythrocyte Ghosts Is Distinct from Viral InactivationPublished by Elsevier ,1996
- Membrane fusion mediated by the influenza virus hemagglutinin requires the concerted action of at least three hemagglutinin trimers.The Journal of cell biology, 1996
- Low-pH induced conformational changes in viral fusion proteins: implications for the fusion mechanismJournal of General Virology, 1995
- Use of resonance energy transfer to monitor membrane fusionBiochemistry, 1981