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Method for Measurement of Viral Fusion Kinetics at the Single Particle Level
Published on: September 7, 2009
Influenza hemagglutinin-mediated membrane fusion does not involve inverted phase lipid intermediates
1Abteilung Biophysikalische Chemie, Universität Basel, Switzerland.
Insights
Influenza hemagglutinin-mediated membrane fusion does not require intermediate lipid structures like those found near lamellar to inverted hexagonal phase transitions. Fusion occurs efficiently even when these structures cannot form.
Area of Science:
- Biophysics
- Membrane Biology
- Virology
Background:
- Intermediate lipid structures, such as inverted micelles, are hypothesized to facilitate membrane fusion.
- These structures typically form near the lamellar (L alpha) to inverted hexagonal (HII) phase boundaries.
Purpose of the Study:
- To investigate the role of L alpha/HII transition intermediates in influenza hemagglutinin (HA)-mediated membrane fusion.
- To determine if specific lipid phases are essential for HA-driven viral fusion.
Main Methods:
- Fusion assays were conducted using influenza virus and liposomes with varying lipid compositions.
- Liposomes were designed to either form or not form HII phases.
- Fusion was measured under conditions where lipid membranes were in gel (L beta') or liquid crystalline (L alpha) phases.
- Reconstituted HA in liposomes was used to assess fusion independent of viral lipids.
Main Results:
- Influenza virus fusion with liposomes unable to form HII phases was only slightly impaired.
- Efficient fusion occurred with liposomes in the gel phase, far from L alpha/HII transitions.
- Reconstituted HA induced fusion below the lipid phase transition temperature, ruling out viral lipid involvement in intermediate formation.
Conclusions:
- Structures resembling intermediates in L alpha/HII transitions are not essential for influenza hemagglutinin-mediated membrane fusion.
- HA-mediated fusion can occur independently of the ability of lipids to form inverted phases.
Abstract:
Intermediate lipid structures such as inverted micelles and interlamellar attachments, which can form near liquid crystalline lamellar (L alpha) to inverted hexagonal (HII) phase boundaries, are thought to play a role in membrane fusion. To investigate whether these structures are also involved in influenza hemagglutinin-mediated membrane fusion, measurement of fusion under conditions where such structures could not form was attempted. It was found that the fusion of influenza virus with liposomal membranes containing phosphatidylcholine and gangliosides, which cannot form HII phases, was only slightly slower than fusion with liposomes that also contained the HII competent phosphatidylethanolamine. Furthermore, the virus fused efficiently with liposomes consisting either of pure saturated phosphatidylcholines or phosphatidylcholine/ganglioside mixtures, even when the liposomal membranes were in the gel (L beta') phase and thus far from L alpha/HII transitions. Isolated hemagglutinin, reconstituted into dimyristoylphosphatidylcholine membranes, induced fusion with liposomes composed of dimyristoylphosphatidylcholine and gangliosides at temperatures below the L beta' to L alpha phase transition temperature of dimyristoylphosphatidylcholine. This latter finding excluded the possibility that the viral lipids alone could have formed inverted phase intermediates, thus enabling them to fuse with liposomes that do not contain lipids capable of forming inverted phases. Therefore, it is concluded that structures resembling intermediates in L alpha/HII transitions are most likely not involved in influenza hemagglutinin-mediated fusion.
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