Role of Target Membrane Structure in Fusion with Influenza Virus: Effect of Modulating Erythrocyte Transbilayer Phospholipid Distribution

References

• Bitbol M., Fellmann P., Zachowski A., Devaux P. F. Ion regulation of phosphatidylserine and phosphatidylethanolamine outside-inside translocation in human erythrocytes. Biochim. Biophys. Acta 1987; 904: 268–282
   PubMed Web of Science ®Google Scholar
• Bligh E. G., Dyer W. J. Lipid extraction using chloroform-methanol. Can. J. Biochem. Physiol. 1959; 37: 911–917
   PubMedGoogle Scholar
• Blumenthal R., Bali-Puri A., Walter A., Covell D., Eidelman O. pH-Dependent fusion of vesicular stomatitis virus with vero cells: measurement by dequenching of octadecylrhodamine fluorescence. J. Biol. Chem. 1987; 262: 13614–13619
   PubMed Web of Science ®Google Scholar
• Blumenthal R., Schoch C., Puri A., Clague M. J. A dissection of steps leading to viral envelope protein-mediated fusion. Ann. NY Acad. Sci. 1991; 635: 285–296
   PubMed Web of Science ®Google Scholar
• Brandts J. F., Erickson L., Lysko K., Schwartz A. T., Taverna R. D. Calorimetric studies of the structural transitions of the human erythrocyte membrane. The involvement of spectrin in the A transition. Biochemistry 1977; 16: 3450–3454
   PubMed Web of Science ®Google Scholar
• Calvez J. Y., Zachowski A., Herrmann A., Devaux P. F. Asymmetric distribution of phospholipids in spectrin-poor erythrocyte vesicles. Biochemistry 1988; 27: 5666–5670
   PubMedGoogle Scholar
• Clague M. J., Schoch C., Blumenthal R. The delay time for influenza hemagglutinin-induced membrane fusion depends on the hemagglutinin surface density. J. Virol. 1991; 65: 2402–2407
   PubMed Web of Science ®Google Scholar
• Clague M. J., Schoch C., Zech L., Blumenthal R. Gating kinetics of pH-activated membrane fusion of vesicular stomatitis virus with cells: stopped flow measurements by dequenching of octadecylrhodamine fluorescence. Biochemistry 1990; 29: 1303–1308
   PubMed Web of Science ®Google Scholar
• Connor J., Gillum K., Schroit A. J. Maintenance of lipid asymmetry in red blood cells and ghosts: effect of divalent cations and serum albumin on the transbilayer distribution of phosphatidylserine. Biochim. Biophys. Acta 1990; 1025: 82–86
   PubMed Web of Science ®Google Scholar
• Deutsch J. W., Kelly R. B. Lipids of synaptic vesicles: relevance to the mechanism of membrane fusion. Biochemistry 1981; 20: 378–385
   PubMedGoogle Scholar
• Doms R. W., Helenius A., White J. Membrane fusion activity of the influenza virus hemagglutinin. The low pH-induced conformational change. J. Biol. Chem. 1985; 260: 2973–2981
   PubMed Web of Science ®Google Scholar
• Dressier V., Schwister K., Haest C. W., Deuticke B. Dielectric breakdown of the erythrocyte membrane enhances transbilayer mobility of phospholipids. Biochim. Biophys. Acta 1983; 732: 304–307
   PubMedGoogle Scholar
• Gething M. J., Sambrook J. Cell-surface expression of influenza haemagglutinin from a cloned DNA copy of the RNA gene. Nature 1981; 293: 620–625
   PubMedGoogle Scholar
• Gudi S. R., Kumar A., Bhakuni V., Gokhale S. M., Gupta C. M. Membrane skeleton-bilayer interaction is not the major determinant of membrane phospholipid asymmetry in human erythrocytes. Biochim. Biophys. Acta 1990; 1023: 63–72
   PubMedGoogle Scholar
• Herrmann A., Clague M. J., Puri A., Morris S. J., Blumenthal R., Grimaldi S. Effect of erythrocyte transbilayer phospholipid distribution on fusion with vesicular stomatitis virus. Biochemistry 1990; 29: 4054–4058
   PubMed Web of Science ®Google Scholar
• Herrmann A., Lassmann G., Groth T., Donath E., Hillebrecht B. Conformational alterations within the glycocalyx of erythrocyte membranes studied by spin labeling. Biochim. Biophys. Acta 1986; 861: 111–121
   PubMed Web of Science ®Google Scholar
• Herrmann A., Zachowski A., Devaux P. F., Blumenthal R. Control of fusion of biological membranes by phospholipid asymmetry. Cell and Model Membrane Interactions, S. Ohki. Plenum Press, New York 1991; 89–114
   Google Scholar
• Hoekstra D., de Boer T., Klappe K., Wilschut J. Fluorescence method for measuring the kinetics of fusion between biological membranes. Biochemistry 1984; 23: 5675–5681
   PubMed Web of Science ®Google Scholar
• Hui S. W., Stewart C. M., Cherry R. J. Electron microscopic observation of the aggregation of membrane proteins in human erythrocyte by melittin. Biochim. Biophys. Acta 1990; 1023: 335–340
   PubMedGoogle Scholar
• Hullin F., Bossant M. J., Salem N., Jr. Aminophospholipid molecular species asymmetry in the human erythrocyte plasma membrane. Biochim. Biophys. Acta 1991; 1061: 15–25
   PubMed Web of Science ®Google Scholar
• Israelachvili J. N., Marcelja S., Horn R. G. Physical principles of membrane organization. Q. Rev. Biophys. 1980; 13: 121–200
   PubMed Web of Science ®Google Scholar
• Li Q. X., Dowhan W. Structural characterization of Escherichia coli phosphatidylserine decarboxylaze. J. Biol. Chem. 1988; 263: 11515–11522
   Google Scholar
• Maeda T., Kawasaki K., Ohnishi S. I. Interaction of influenza hemagglutinin with target membrane lipids is a key step in virus-induced hemolysis and fusion at pH 5.2. Proc. Natl. Acad. Sci. USA 1981; 78: 4133–4137
   PubMed Web of Science ®Google Scholar
• McEvoy L., Williamson P., Schlegel R. A. Membrane phospholipid asymmetry as a determinant of erythrocyte recognition by macrophages. Proc. Natl. Acad. Sci. USA 1986; 83: 3311–3315
   PubMed Web of Science ®Google Scholar
• Morris S. J., Sarkar D. P., White J. M., Blumenthal R. Kinetics of pH-dependent fusion between 3T3 fibroblasts expressing influenza hemagglutinin and red blood cells. J. Biol. Chem. 1989; 264: 3972–3978
   PubMed Web of Science ®Google Scholar
• Ohki S. Surface tension, hydration energy and membrane fusion. Molecular Mechanisms of Membrane Fusion, S. Ohki, D. Doyle, T. D. Flanagan, S. W. Hui, E. Mayhew. Plenum Press, New York 1988; 123–139
   Google Scholar
• Sarkar D. P., Morris S. J., Eidelman O., Zimmerberg J., Blumenthal R. Initial stages of influenza hemagglutinin-induced cell fusion monitored simultaneously by two fluorescent events: cytoplasmic continuity and lipid mixing. J. Cell Biol. 1989; 109: 113–122
   PubMed Web of Science ®Google Scholar
• Seigneuret M., Devaux P. F. ATP-dependent asymmetric distribution of spin-labeled phospholipids in the erythrocyte membrane: relation to shape changes. Proc. Natl. Acad. Sci. USA 1984; 81: 3751–3755
   PubMed Web of Science ®Google Scholar
• Seigneuret M., Zachowski A., Herrmann A., Devaux P. F. Asymmetric lipid fluidity in human erythrocyte membrane: new spin-label evidence. Biochemistry 1984; 23: 4271–4275
   PubMed Web of Science ®Google Scholar
• Sessions A., Horwitz A. F. Differentiation-related differences in the plasma membrane phospholipid asymmetry of myogenic and fibrogenic cells. Biochim. Biophys. Acta 1983; 728: 103–111
   PubMedGoogle Scholar
• Skehel J. J., Bayley P. M., Brown E. B., Martin S. R., Waterfield M. D., White J. M., Wilson I. A., Wiley D. C. Changes in the conformation of influenza virus hemagglutinin at the pH optimum of virus-mediated membrane fusion. Proc. Natl. Acad. Sci. USA 1982; 79: 968–972
   PubMed Web of Science ®Google Scholar
• Spruce A. E., Iwata A., Aimers W. The first milliseconds of the pore formed by a fusogenic viral envelope protein during membrane fusion. Proc. Natl. Acad. Sci. USA 1991; 88: 3623–3627
   PubMed Web of Science ®Google Scholar
• Stegmann T., Hoekstra D., Scherphof G., Wilschut J. Fusion activity of influenza virus. A comparison between biological and artificial target membrane vesicles. J. Biol. Chem. 1986; 261: 10966–10969
   PubMed Web of Science ®Google Scholar
• Stegmann T., White J. M., Helenius A. Intermediates in influenza-induced membrane fusion. EMBO J. 1990; 9: 4231–4241
   PubMed Web of Science ®Google Scholar
• Stubbs C. D., Smith A. D. The modification of mammalian membrane polyunsaturated fatty acid composition in relation to membrane fluidity and function. Biochim. Biophys. Act 1984; 779: 89–137
   PubMed Web of Science ®Google Scholar
• Tanaka K. I., Ohnishi S. Heterogeneity in the fluidity of intact erythrocyte membrane and its homogenization upon hemolysis. Biochim. Biophys. Acta 1976; 426: 218–231
   PubMed Web of Science ®Google Scholar
• Tullius E. K., Williamson P., Schlegel R. A. Effect of transbilayer phospholipid distribution on erythrocyte fusion. Biosci. Rep. 1989; 9: 623–633
   PubMedGoogle Scholar
• van Meer G., Davoust J., Simons K. Parameters affecting low-pH-mediated fusion of liposomes with the plasma membrane of cells infected with influenza virus. Biochemistry 1985; 24: 3593–3602
   PubMed Web of Science ®Google Scholar
• Verhoeven B. M., Schlegel R. A., Williamson P. (1990) Lipid asymmetry in erythrocytes is rapidly lost and regained. Internal. Biophys. Congress, VancouverCanada, 1990, 353, (Abstract)
   Google Scholar
• White J., Kartenbeck J., Helenius A. Membrane fusion activity of influenza virus. EMBO J. 1982; 1: 217–222
   PubMed Web of Science ®Google Scholar
• White J., Kielian M., Helenius A. Membrane fusion proteins of enveloped animal viruses. Q. Rev. Biophys. 1983; 16: 151–195
   PubMed Web of Science ®Google Scholar
• Williams J. H., Kuchmak M., Witter R. F. Fatty acids in phospholipids isolated from human red cells. Lipids 1966; 1: 391–398
   PubMedGoogle Scholar
• Williamson P., Algarin L., Bateman J., Choe H. R., Schlegel R. A. Phospholipid asymmetry in human ghost erythrocytes. J. Cell Physiol. 1985; 123: 209–214
   PubMedGoogle Scholar
• Yoshino H., Minari O. Heat-induced dissociation of human erythrocyte spectrin dimer into monomers. Biochim. Biophys. Acta 1987; 905: 100–108
   PubMedGoogle Scholar
• Zwaal R. F., Roelofsen B., Comfurius P., van Deenen L. L. Organization of phospholipids in human red cell membranes as detected b y the action of various purified phospholipases. Biochim. Biophys. Acta 1975; 406: 83–96
   PubMedGoogle Scholar