Viral Membranes: Model Systems for Studying Biological Membrane

References

• Danielli J. F., Davson H. A contribution to the theory of permeability of thin film. J. Cell. Comp. Physiol. 1935; 5: 495
   Google Scholar
• Singer S. J. The molecular organization of membrane. Annu. Rev. Biochem. 1974; 43: 805
   PubMed Web of Science ®Google Scholar
• Fenner F. Classification and nomenclature of viruse. Second Report of the International Committee on Taxonomy of Viruses. S. Karger, Basel 1976
   Google Scholar
• Lenard J., Compans R. W. The membrane structure of lipid-containing viruse. Biochim. Biophys. Acta 1974; 334: 5194
   Google Scholar
• Lenard J. Virus envelopes and plasma membrane. Annu. Rev. Biophys. Bioeng. 1978; 7: 139
   PubMedGoogle Scholar
• Rott R., Klenk H.-D. Structure and assembly of viral envelope. Virus Infection and the Cell Surface, G. Poste, G. L. Nicholson. North-Holland, Amsterdam 1977; 47
   Google Scholar
• Compans R. W., Klenk H.-D. Viral membrane. Comprehensive Virology, H. Fraenkel-Conrat, R. R. Wagner. Plenum Press, New York, Vol. 13, in press
   Google Scholar
• Moss B. Reproduction of poxviruse. Comprehensive Virology, H. Fraenkel-Conrat, R. R. Wagner. Plenum Press, New York 1974; Vol. 3: 405
   Google Scholar
• Diener T. O., Hadidi A. Viroid. Comprehensive Virology, H. Fraenkel-Conrat, R. R. Wagner. Plenum Press, New York 1977; Vol. 11: 285
   Google Scholar
• Gross H. J., Domdey H., Lassow C., Jank P., Raba M., Alberty A., Sänger H. L. Nucleotide sequence and secondary structure of potato spindle tuber viroi. Nature (London) 1978; 273: 203
   PubMed Web of Science ®Google Scholar
• Wagner R. R. Reproduction of rhabdoviruse. Comprehensive Virology, H. Fraenkel-Conrat, R. R. Wagner. Plenum Press, New York 1975; Vol. 4: 1
   Google Scholar
• McSharry J. J., Wagner R. R. Lipid composition of purified vesicular stomatitis viru. J. Virol. 1971; 7: 59
   PubMed Web of Science ®Google Scholar
• Choppin P. W., Compans R. W. Reproduction of paramyxoviruse. Comprehensive Virology. Plenum Press, New York 1975; Vol. 4: 95
   Google Scholar
• Klenk H.-D., Choppin P. W. Plasma membrane lipids and parainfluenza virus assembl. Virology 1970; 40: 939
   PubMed Web of Science ®Google Scholar
• Compans R. W., Choppin P. W. Reproduction of myxoviruse. Comprehensive Virology, H. Fraenkel-Conrat, R. R. Wagner. Plenum Press, New York 1975; Vol. 4: 179
   Google Scholar
• Kilbourne E. D. The Influenza Viruses and Influenza. Academic Press, New York 1975
   Google Scholar
• Rawls W. E. Arenaviruse. Comprehensive Virology, H. Fraenkel-Conrat, R. R. Wagner. Plenum Press, New York, Vol. 14, in press
   Google Scholar
• Vezza A. C., Gard G. P., Compans R. W., Bishop D. H. L. Structural components of the arenavirus Pichind. J. Virol. 1977; 23: 776
   PubMed Web of Science ®Google Scholar
• Pfefferkorn E. R., Shapiro D. Reproduction of togaviruse. Comprehensive Virology, H. Fraenkel-Conrat, R. R. Wagner. Plenum Press, New York 1974; Vol. 2: 171
   Google Scholar
• Luukkonenen A., von Bondsdorff C.-H., Renkonen O. Characterization of Semliki Forest virus grown in mosquito cells. Comparison with virus from hamster cell. Virology 1977; 78: 331
   PubMed Web of Science ®Google Scholar
• Bishop D. H. L., Shope R. E. Bunyaviruse. Comprehensive Virology, H. Fraenkel-Conrat, R. R. Wagner. Plenum Press. Vol. 14, in press
   Google Scholar
• von Bonsdorff C. H., Pettersson R. Surface structure of Uukuniemi viru. J. Virol. 1975; 16: 1296
   PubMed Web of Science ®Google Scholar
• Gentsch J., Bishop D. H. L., Obijeski J. F. The virus particle nucleic acids and proteins of four bunyaviruse. J. Gen. Virol. 1977; 34: 257
   PubMed Web of Science ®Google Scholar
• Robb J. A., Bond C. W. Coronavirida. Comprehensive Virology, H. Fraenkel-Conrat, R. R. Wagner. Plenum Press, New York, Vol. 14, in press
   Google Scholar
• Sturman L. S., Holmes K. V. Characterization of a coronavirus. II. Glycoproteins of the viral envelope: tryptic peptide analysi. Virology 1977; 77: 650
   PubMed Web of Science ®Google Scholar
• Bingham R. W., Almeida J. D. Studies on the structure of a coronavirus: avian infectious bronchitis viru. J. Gen. Virol. 1977; 36: 495
   PubMed Web of Science ®Google Scholar
• Quigley J. P., Rifkin D. B., Reich E. Phospholipid composition of Rous sarcoma virus, host cell membranes, and other enveloped RNA viruse. Virology 1972; 46: 106
   Web of Science ®Google Scholar
• Bolognesi D. P. Structural components of RNA tumor viruse. Adv. Virus Res. 1974; 19: 315
   PubMedGoogle Scholar
• Witte O. N., Baltimore D. Relationship of retrovirus polyprotein cleavages to virion maturation studied with temperature-sensitive murine leukemia virus mutant. J. Virol. 1978; 26: 750
   PubMed Web of Science ®Google Scholar
• Moss B., Rosenblum E. N., Garon C. F. Glycoprotein synthesis in cells infected with vaccinia virus. III. Purification and biosynthesis of the virion glycoprotei. Virology 1973; 55: 143
   PubMed Web of Science ®Google Scholar
• Stern W., Dales S. Biogenesis of vaccinia: concerning the origin of the envelope phospholipid. Virology 1974; 62: 293
   PubMed Web of Science ®Google Scholar
• Stern W., Dales S. Biogenesis of vaccinia: isolation and characterization of a surface component that elicits antibody-suppressing activity and cell-cell fusio. Virology 1976; 75: 232
   PubMed Web of Science ®Google Scholar
• Goorha R., Granoff A. Icosahedral cytoplasmic deoxyviruse. Comprehensive Virology, H. Fraenkel-Conrat, R. R. Wagner. Plenum Press, New York, Vol. 14, in press
   Google Scholar
• Kelly D. C., Robertson J. S. Icosahedral cytoplasmic deoxyviruse. J. Gen. Virol. 1973; 20: 17
   PubMed Web of Science ®Google Scholar
• McAuslan B. R., Armentrout R. W. The biochemistry of icosahedral cytoplasmic deoxyviruse. Curr. Top. Microbiol. Immunol. 1974; 68: 77
   Google Scholar
• Roizman B., Furlong D. The replication of herpesviruse. Comprehensive Virology, H. Fraenkel-Conrat, R. R. Wagner. Plenum Press, New York 1974; Vol. 3: 229
   Google Scholar
• Spear P. C. Membrane proteins specified by herpes simplex viruses. I. Identification of four glycoprotein precursors and their products in type-1-infected cell. J. Virol. 1976; 17: 991
   PubMed Web of Science ®Google Scholar
• O'Callaghan D. J., Randall C. C. Molecular anatomy of herpesviruses: recent studie. Prog. Med. Virol. 1976; 22: 152
   PubMedGoogle Scholar
• Maniloff J., Das J., Christensen J. R. Viruses of mycoplasmas and spiroplasma. Adv. Virus Res. 1977; 21: 343
   PubMedGoogle Scholar
• Mindich L. Bacteriophages that contain lipi. Comprehensive Virology, H. Fraenkel-Conrat, R. R. Wagner. Plenum Press, New York 1977; Vol. 12: 271
   Google Scholar
• Harrison S. C., David A., Jumblatt J., Darnell J. E. Lipid and protein organization in Sindbis viru. J. Mol. Biol. 1971; 60: 523
   Web of Science ®Google Scholar
• Landsberger F. R., Lenard J., Paxton J., Compans R. W. Spin-label electron spin resonance study of the lipid-containing membrane of influenza viru. Proc. Natl. Acad. Sci. U.S.A. 1971; 68: 2579
   PubMed Web of Science ®Google Scholar
• Pike B. V., Garwes D. J. Lipids of transmissible gastroenteritis virus and their relation to those of two different host cell. J. Gen. Virol. 1977; 34: 531
   PubMed Web of Science ®Google Scholar
• Ben-Porat T., Kaplan A. S. Phospholipid metabolism of herpesvirus-infected and uninfected rabbit kidney cell. Virology 1971; 45: 252
   PubMed Web of Science ®Google Scholar
• Klenk H.-D., Choppin P. W. Lipids of plasma membranes of monkey and hamster kidney cells and of parainfluenza virions grown in these cell. Virology 1969; 38: 255
   PubMed Web of Science ®Google Scholar
• Klenk H.-D., Choppin P. W. Plasma membrane lipids and parainfluenza virus assembl. Virology 1970; 40: 939
   PubMed Web of Science ®Google Scholar
• Patzer E. J., Moore N. F., Barenholz Y., Shaw J. M., Wagner R. R. Lipid organization of the membrane of vesicular stomatitis viru. J. Biol. Chem. 1978; 253: 4544
   PubMed Web of Science ®Google Scholar
• Blough H. A., Tiffany J. M., Aaslestad H. G. Lipids of rabies virus and BHK-21 cell membrane. J. Virol. 1977; 21: 950
   PubMed Web of Science ®Google Scholar
• Schlesinger H. L., Wells H. J., Hummeler K. Comparison of the lipids of intracellular and extracellular rabies viru. J. Virol. 1973; 12: 1028
   PubMed Web of Science ®Google Scholar
• Quigley J. P., Rifkin D. B., Reich E. Lipid studies of Rous sarcoma virus and cell membrane. Virology 1972; 50: 550
   PubMed Web of Science ®Google Scholar
• Renkonen O., Käärïäinen L., Simons K., Gahmberg C. O. The lipid class composition of Semliki Forest virus and of plasma membranes of host cell. Virology 1971; 46: 318
   PubMed Web of Science ®Google Scholar
• Hirschberg C. B., Robbins P. W. The glycolipids and phospholipids of Sindbis virus and their relation to the lipids of the host cell plasma membran. Virology 1974; 61: 602
   PubMed Web of Science ®Google Scholar
• Klenk H.-D. Virus membrane. Biological Membranes, D. Chapman, D. F. Holzel-Wallach. Academic Press, London 1973; 145
   Google Scholar
• St Geme J. W., Jr., Martin H. L., Davis C. W., Mead J. F. A biochemical concept of cellular production of paramyxoviruse. Pediatr. Res. 1977; 11: 174
   PubMed Web of Science ®Google Scholar
• Tiffany J. M., Blough H. A. Fatty acid composition of three strains of Newcastle disease viru. Virology 1969; 37: 492
   PubMed Web of Science ®Google Scholar
• Tiffany J. M., Blough H. A. Myxovirus envelope proteins: a directing influence on the fatty acids of membrane lipid. Science 1969; 163: 573
   PubMed Web of Science ®Google Scholar
• Lindenmann J. Host antigens in enveloped RNA viruse. Virus Infection and the Cell Surface, G. Poste, G. L. Nicolson. North-Holland, New York 1977; 291
   Google Scholar
• Klenk H.-D., Choppin P. W. Glycosphingolipids of plasma membranes of cultured cell and an enveloped virus (SV5) grown in these cell. Proc. Natl. Acad. Sci. U.S.A. 1970; 66: 57
   PubMed Web of Science ®Google Scholar
• Klenk H.-D., Choppin P. W. Glycolipid content of vesicular stomatitis virus grown in baby hamster kidney cell. J. Virol. 1971; 7: 416
   PubMed Web of Science ®Google Scholar
• Cartwright B., Brown F. Glycolipid nature of the complement-fixing host cell antigen of vesicular stomatitis viru. J. Gen. Virol. 1972; 15: 243
   PubMed Web of Science ®Google Scholar
• Bretscher M. S. Phosphatidyl-ethanolamine: differential labeling in intact cells and cell ghosts of human erythrocytes by a membrane-impermeable reagent (FMMP. J. Mol. Biol. 1972; 71: 523
   PubMed Web of Science ®Google Scholar
• Bretscher M. S. Asymmetrical lipid bilayer structure for biological membrane. Nature (London) 1972; 236: 11
   Web of Science ®Google Scholar
• Bergelson L. D., Barsukov L. I. Topological asymmetry of phospholipids in membrane. Science 1977; 197: 224
   PubMed Web of Science ®Google Scholar
• Rothman J. E., Lenard J. Membrane asymmetry. The nature of membrane asymmetry provides clues to the puzzle of how membranes are assemble. Science 1977; 195: 743
   PubMed Web of Science ®Google Scholar
• Tsai D. K., Lenard J. Asymmetry of influenza virus membrane bilayer demonstrated with phospholipase . Nature (London) 1975; 253: 554
   PubMed Web of Science ®Google Scholar
• Rothman J. E., Tsai D. K., Dawidowicz E. A., Lenard J. Transbilayer phospholipid asymmetry and its maintenance in the membrane of influenza viru. Biochemistry 1976; 15: 2361
   PubMed Web of Science ®Google Scholar
• Fong B. S., Hunt R. C., Brown J. C. Assymmetric distribution of phosphatidylethanolamine in the membrane of vesicular stomatitis viru. J. Virol. 1976; 20: 658
   PubMed Web of Science ®Google Scholar
• Shaw J. M., Moore N. F., Patzer E. J., Correa-Freire M., Thompson T. E., Wagner R. R. Transmembrane novement and asymmetry of phosophatidylcholine in the membrane of vesicular stomatitis viru. Biochemistry., 18, in press
   Google Scholar
• Gahmberg C. G., Simons K., Renkonen O., Kääriäïnen L. Exposure of proteins and lipids in the Semliki Forest virus membran. Virology 1972; 50: 259
   PubMed Web of Science ®Google Scholar
• Sandra A., Pagano R. E. Phospholipid asymmetry in LM cell plasma membrane derivatives: polar headgroup and acyl chain distribution. Biochemistry 1978; 17: 332
   PubMed Web of Science ®Google Scholar
• Chap H. J., Zwaal R. F. A., van Deenen L. L. M. Action of highly purified phospholipases on blood platelets. Evidence for an asymmetric distribution of phospholipids in the surface membran. Biochim. Biophys. Acta 1977; 467: 146
   PubMed Web of Science ®Google Scholar
• Palade G. E. Intracellular aspects of the process of protein synthesi. Science 1975; 189: 347
   PubMed Web of Science ®Google Scholar
• Nilsson O. S., Dallner G. Transverse asymmetry of phospholipids in subcellular membranes of rat live. Biochim. Biophys. Acta 1977; 464: 453
   PubMedGoogle Scholar
• Higgins J. A., Dawson R. M. C. Asymmetry of the phospholipid bilayer of rat liver endoplasmic reticulu. Biochim. Biophys. Acta 1977; 470: 342
   PubMedGoogle Scholar
• Vale M. G. P. Localization of the amino phospholipids in sarcoplasmic reticulum membranes revealed by trinitrobenzenesulfonate and fluorodinitrobenzen. Biochim. Biophys. Acta 1977; 471: 39
   PubMed Web of Science ®Google Scholar
• Hidalgo C., Ikemoto N. Disposition of proteins and amino-phospholipids in the sarcoplasmic reticulum membran. J. Biol. Chem. 1977; 252: 8446
   PubMed Web of Science ®Google Scholar
• Renooij W., van Golde L. M. G. The transposition of molecular classes of phosphatidylcholine across the rat erythrocyte membrane and their exchange between the red cell membrane and plasma lipoprotein. Biochim. Biophys. Acta 1977; 470: 465
   PubMedGoogle Scholar
• Gottlieb M. H. The reactivity of human erythrocyte membrane cholesterol with a cholesterol oxidas. Biochim. Biophys. Acta 1977; 466: 422
   PubMedGoogle Scholar
• Patzer E. J., Wagner R. R., Barenholz Y. Cholesterol oxidase as a probe for studying membrane organizatio. Nature (London) 1978; 274: 394
   PubMed Web of Science ®Google Scholar
• Barenholz Y., Patzer E. J., Moore N. F., Wagner R. R. Cholesterol oxidase as a probe for studying membrane composition and organizatio. Enzymes of Lipid Metabolism, S. Gatt, L. Freysz, P. Mandel. Plenum Press, New York 1978; 45
   Google Scholar
• Lenard J., Rothman J. E. Transbilayer distribution and movement of cholesterol and phospholipid in the membrane of influenza viru. Proc. Natl. Acad. Sci. U.S.A. 1976; 73: 391
   PubMed Web of Science ®Google Scholar
• Moore N. F., Patzer E. J., Barenholz Y., Wagner R. R. Effect of phospholipase C and cholesterol oxidase in membrane integrity, microviscosity and infectivity of vesicular stomatitis viru. Biochemistry 1977; 16: 4708
   PubMed Web of Science ®Google Scholar
• Patzer E. J., Shaw J. M., Moore N. F., Thompson T. E., Wagner R. R. Transmembrane movement and distribution of cholesterol in the membrane of vesicular stomatitis viru. Biochemistry 1978; 17: 4192
   PubMed Web of Science ®Google Scholar
• Bruckdorfer K. R., Edwards P. A., Green C. Properties of aqueous dispersions of phospholipid and cholestero. Eur. J. Biochem. 1968; 4: 506
   PubMedGoogle Scholar
• Grünze M., Deuticke B. Changes of membrane permeability due to extensive cholesterol depletion in mammalian erythrocyte. Biochim. Biophys. Acta 1974; 356: 125
   PubMed Web of Science ®Google Scholar
• Gottlieb M. H. The limited depletion of cholesterol from erythrocyte membranes on treatment with incubated plasm. Biochim. Biophys. Acta 1976; 433: 333
   Google Scholar
• Fisher K. A. Analysis of membrane halves: cholestero. Proc. Natl. Acad. Sci. U.S.A. 1976; 73: 173
   PubMed Web of Science ®Google Scholar
• Razin S., Rottem S. Cholesterol in membranes: studies with mycoplasma. Trends Biochem. Sci. 1978; 3: 51
   Web of Science ®Google Scholar
• Gahmberg C. G., Hakamori S. I. External labeling of cell surface galactose and galactosamine in glycolipid and glycoprotein of human erythrocyte. J. Biol. Chem. 1973; 248: 4311
   PubMed Web of Science ®Google Scholar
• Steck T. L., Dawson G. Topographical distribution of complex carbohydrates in the erythrocyte membran. J. Biol. Chem. 1974; 249: 2135
   PubMed Web of Science ®Google Scholar
• Stoffel W., Anderson R., Stahl J. Studies on the asymmetric arrangement of membrane-lipid-enveloped virions as a model syste. Hoppe Seylers Z. Physiol. Chem. 1975; 356: 1123
   PubMedGoogle Scholar
• Klenk H.-D., Rott R., Becht H. On the structure of the influenza virus envelop. Virology 1972; 47: 579
   PubMed Web of Science ®Google Scholar
• Johnson L. W., Hughes M. E., Zilversmit D. B. 1975, Use of phospholipid exchange protein to measure inside-outside transposition in phosphatidylcholine liposome. Biochim. Biophys. Acta 1975; 375: 176
   PubMed Web of Science ®Google Scholar
• Roseman M., Litman B. J., Thompson T. E. Transbilayer exchange of phosphatidylethanolamine for phosphatidylcholine and N-acetimidoylphosphatidylethanolamine in single-walled bilayer vesicle. Biochemistry 1975; 14: 4826
   PubMed Web of Science ®Google Scholar
• Rothman J. E., Dawidowicz E. A. Asymmetric exchange of vesicle phospholipids catalyzed by the phosphatidylcholine exchange protein. Measurement of inside-outside transition. Biochemistry 1975; 14: 2809
   PubMed Web of Science ®Google Scholar
• Shaw J. M., Hutton W. C., Lentz B. R., Thompson T. E. Proton nuclear magnetic resonance study of the decay of transbilayer compositional asymmetry generated by a phosphatidylcholine exchange protei. Biochemistry 1977; 16: 4156
   PubMed Web of Science ®Google Scholar
• Rothman J. E., Kennedy E. P. Rapid transmembrane movement of newly synthesized phospholipids during membrane assembl. Proc. Natl. Acad. Sci. U.S.A. 1977; 74: 1821
   PubMed Web of Science ®Google Scholar
• Zilversmit D. B., Hughes M. E. Extensive exchange of rat liver microsomal phospholipid. Biochim. Biophys. Acta 1977; 469: 99
   PubMedGoogle Scholar
• Renooij W., van Golde L. M. G., Zwaal R. F. A., van Deenen L. L. M. Topological asymmetry of phospholipid metabolism in rat erythrocyte membrane. Eur. J. Biochem. 1976; 61: 53
   PubMedGoogle Scholar
• Bloj B., Zilversmit D. B. Complete exchangeability of cholesterol in phosphatidylcholine/cholesterol vesicles of different degrees of unsaturatio. Biochemistry 1977; 16: 3943
   PubMed Web of Science ®Google Scholar
• Rousselet A., Guthmann C., Matricon J., Bienvenue A., Devaux P. F. Study of transverse diffusion of spinlabeled phospholipids in biological membranes. I. Human red blood cell. Biochim. Biophys. Acta 1976; 426: 357
   PubMedGoogle Scholar
• Van Zoelen E. J. J., De Kruijff B., van Deenen L. L. M. Protein-mediated transbilayer movement of lysophosphatidylcholine in glycophorin containing vesicle. Biochim. Biophys. Acta 1978; 508: 97
   PubMedGoogle Scholar
• Poznansky M. J., Lange Y. Transbilayer movement of cholesterol in dipalmitoyllecithin-cholesterol vesicle. Nature (London) 1976; 259: 420
   PubMed Web of Science ®Google Scholar
• Poznansky M. J., Lange Y. Transbilayer movement of cholesterol in phospholipid vesicles under equilibrium and non-equilibrium condition. Biochim. Biophys. Acta 1978; 506: 256
   PubMedGoogle Scholar
• Lange Y., Cohen C. M., Poznansky M. J. Transmembrane movement of cholesterol in human erythrocyte. Proc. Natl. Acad. Sci. U.S.A. 1977; 74: 1538
   PubMed Web of Science ®Google Scholar
• Devaux P., McConnell H. M. Lateral diffusion in spinlabeled phosphatidylcholine multilayer. J. Am. Chem. Soc. 1972; 94: 4475
   PubMed Web of Science ®Google Scholar
• Shinitzky M., Barenholz Y. Dynamics of the hydrocarbon layer in liposomes of lecithin and sphingomyelin containing dicetylphosphat. J. Biol. Chem. 1974; 249: 2652
   PubMed Web of Science ®Google Scholar
• Landsberger F. R., Compans R. W. Effect of membrane protein on lipid bilayer structure: a spin-label electron spin reasonance study of vesicular stomatitis viru. Biochemistry 1976; 15: 2356
   PubMed Web of Science ®Google Scholar
• Sefton B. M., Gaffney B. J. Effect of the viral proteins on the fluidity of the membrane lipids in Sindbis viru. J. Mol. Biol. 1974; 90: 343
   PubMed Web of Science ®Google Scholar
• Barenholz Y., Moore N. F., Wagner R. R. Enveloped viruses as model membrane systems: microviscosity of vesicular stomatitis virus and host cell membrane. Biochemistry 1976; 15: 3563
   PubMed Web of Science ®Google Scholar
• Moore N. F., Barenholz Y., McAllister P. E., Wagner R. R. Comparative membrane microviscosity of fish and mammalian rhabdoviruses studied by fluorescence depolarizatio. J. Virol. 1976; 19: 275
   PubMedGoogle Scholar
• Moore N. F., Barenholz Y., Wagner R. R. Microviscosity of togavirus membranes studied by fluorescence depolarization: influence of envelope proteins and the host cel. J. Virol. 1976; 19: 126
   PubMed Web of Science ®Google Scholar
• Van Blitterswijk W. J., Emmelot P., Hilkmann H. A. M., Oomen-Meulemans E. P. M., Inbar M. Differences in lipid fluidity among isolated plasma membranes of normal and leukemic lymphocytes and membranes exfoliated from their cell surfac. Biochim. Biophys. Acta 1977; 467: 309
   PubMedGoogle Scholar
• Esko J. D., Gilmore J. R., Glaser M. Use of a fluorescent probe to determine the viscosity of LM cell membranes with altered phospholipid composition. Biochemistry 1977; 16: 1881
   PubMed Web of Science ®Google Scholar
• Ladbrooke B. D., Chapman D. Thermal analysis of lipids, proteins and biological membranes. A review and summary of some recent studie. Chem. Phys. Lipids 1969; 3: 304
   PubMed Web of Science ®Google Scholar
• Chapman D., Wallach D. F. H. Biological Membranes, D. Chapman. Academic Press, London 1968; 125
   Google Scholar
• Lenard J., Tsai D. K., Compans R. W., Landsberger F. R. Observations on the membrane organization of standard and incomplete influenza grown in MDBK cell. Virology 1976; 71: 389
   PubMed Web of Science ®Google Scholar
• Lenard J., Compans R. W. Polypeptide composition of incomplete influenza virus grown in MDBK cell. Virology 1975; 65: 418
   PubMed Web of Science ®Google Scholar
• Lenard J., Wong C. Y., Compans R. W. Association of the internal membrane protein with the lipid bilayer in influenza virus. A study with the fluorescent probe 12-(9-anthroyl)-stearic aci. Biochim. Biophys. Acta 1974; 332: 341
   Google Scholar
• Landsberger F. R., Compans R. W., Choppin P. W., Lenard J. Organization of the lipid phase in viral membranes. Effects of independent variation of the lipid and the protein compositio. Biochemistry 1973; 12: 4498
   PubMed Web of Science ®Google Scholar
• Stoffel W., Bister K. 13C nuclear magnetic resonance studies on the lipid organization in enveloped virions (vesicular stomatitis virions. Biochemistry 1975; 14: 2841
   PubMed Web of Science ®Google Scholar
• Stoffel W., Bister K., Schreiber C., Tunggal B. 3C NMR studies of the membrane structure of enveloped virion. Hoppe Seylers Z. Physiol. Chem. 1976; 357: 905
   PubMedGoogle Scholar
• Patzer E. J., Schmidt C., Wagner R. R., unpublished data
   Google Scholar
• Moore N. F., Patzer E. J., Wagner R. R., Yeagle P. L., Hutton W. C., Martin R. B. The structure of vesicular stomatitis virus membrane — A phosphorus nuclear magnetic resonance approac. Biochim. Biophys. Acta 1977; 464: 234
   PubMedGoogle Scholar
• Keith A. D., Snipes W. Dynamic apsects of biological membrane. Horiz. Biochem. Biophys. 1977; 4: 31
   PubMedGoogle Scholar
• Gennis R. B., Jonas A. Protein-lipid interaction. Annu. Rev. Biophys. Bioeng. 1977; 6: 195
   PubMedGoogle Scholar
• Utermann G., Simons K. Studies on the amphipathic nature of the membrane proteins in Semliki Forest viru. J. Mol. Biol. 1974; 85: 569
   PubMed Web of Science ®Google Scholar
• Mudd J. A. Glycoprotein fragment associated with vesicular stomatitis virus after proteolytic digestio. Virology 1974; 62: 573
   PubMed Web of Science ®Google Scholar
• Schloemer R. H., Wagner R. R. Association of vesicular stomatitis virus glycoprotein with virion membranes: characterization of the lipophilic tail fragmen. J. Virol. 1975; 16: 237
   PubMed Web of Science ®Google Scholar
• Hosaka Y., Shimizu Y. K. Artificial assembly of envelope particles of HVJ (Sendai virus). I. Assembly of hemolytic and fusion factors from envelopes solubilized by Nonidet P4. Virology 1972; 49: 627
   PubMed Web of Science ®Google Scholar
• Hosaka Y., Shimizu Y. K. Artificial assembly of envelope particles of HVJ (Sendai virus). II. Lipid components for formation of the active hemolysi. Virology 1972; 49: 640
   PubMed Web of Science ®Google Scholar
• Hosaka Y., Semba T., Fukai K. Artificial assembly of envelope particles of HVJ (Sendai virus). Fusion activity of envelope particle. J. Gen. Virol. 1974; 25: 391
   PubMed Web of Science ®Google Scholar
• Hall W. W., Martin S. J. The biochemical and biological characteristics of the surface components of measles viru. J. Gen. Virol. 1974; 22: 363
   PubMed Web of Science ®Google Scholar
• Martin F., MacDonald R. Liposomes can mimic virus membrane. Nature (London) 1974; 252: 161
   PubMed Web of Science ®Google Scholar
• Martin F., MacDonald R. C. Lipid vesicle — cell interactions. 1. Hemagglutination and hemolysi. J. Cell Biol. 1976; 70: 494
   PubMed Web of Science ®Google Scholar
• Martin F., MacDonald R. C. Lipid vesicle-cell interactions. II. Induction of cell fusio. J. Cell Biol. 1976; 70: 506
   PubMed Web of Science ®Google Scholar
• Almeida J. D., Edwards D. C., Brand C. M., Heath T. D. Formation of virosomes from influenza subunits and liposome. Lancet 1975; 2: 899
   PubMed Web of Science ®Google Scholar
• Ichihashi Y. Vaccinia-specific hemagglutinatio. Virology 1977; 76: 527
   PubMed Web of Science ®Google Scholar
• Smith E. C., Pratt B. C., Baxby D. In vitro dissociation and reconstitution of poxvirus hemagglutini. J. Gen. Virol. 1973; 18: 111
   PubMed Web of Science ®Google Scholar
• Bishop D. H. L., Repik P., Obijeski J. F., Moore N. F., Wagner R. R. Restitution of infectivity to spikeless vesicular stomatitis virus by solubilized viral component. J. Virol. 1975; 16: 75
   PubMed Web of Science ®Google Scholar
• Helenius A., Fries E., Kartenbeck J. Reconstitution of Semliki Forest virus membran. J. Cell Biol. 1977; 75: 866
   PubMed Web of Science ®Google Scholar
• Jost P. C., Capaldi R. A., Vanderkooi G., Griffith O. H. Lipid-protein and lipid-lipid interactions in cytochrome oxidase model membrane. J. Supramol. Struct. 1973; 1: 269
   PubMedGoogle Scholar
• Griffith O. H., Jost P., Capaldi R. A., Vanderkooi G. Boundary lipid and fluid bilayer regions in cytochrome oxidase model membrane. Ann. N. Y. Acad. Sci. 1973; 222: 561
   PubMed Web of Science ®Google Scholar
• Dehlinger P. J., Jost P. C., Griffith O. H. Lipid binding to the amphipathic membrane protein cytochrome b5. Proc. Natl. Acad. Sci. U.S.A. 1974; 71: 2280
   PubMed Web of Science ®Google Scholar
• Brulet P., McConnell H. M. Protein-lipid interactions: glycophorin and dipalmitoylphosphatidylcholin. Biochem. Biophys. Res. Commun. 1976; 68: 363
   PubMed Web of Science ®Google Scholar
• Armitage I. M., Shapiro D. L., Furthmayr H., Marchesi V. T. 31P Nuclear magnetic resonance evidence for polyphosphoinositide associated with the hydrophobic segment of glycophorin . Biochemistry 1977; 16: 1317
   PubMed Web of Science ®Google Scholar
• Brown D. T., Riedl B. Morphogenesis of vesicular stomatitis virus: electron microscope observations with freeze-fracture technique. J. Virol. 1977; 21: 1601
   Web of Science ®Google Scholar
• Birrell G. B., Griffith O. H. Cytochrome C induced lateral phase separation in a diphosphatidylglycerolsteroid spin-label model membran. Biochemistry 1976; 15: 2925
   PubMed Web of Science ®Google Scholar
• Morrison T. G., McQuain C. Assembly of viral membranes. I. Association of vesicular stomatitis virus membrane proteins and membranes in a cell-free syste. J. Virol. 1977; 21: 451
   PubMed Web of Science ®Google Scholar
• Kohn A., Klibansky C. Studies on the inactivation of cell-fusing property of Newcastle disease virus by phospholipase . Virology 1967; 31: 385
   PubMed Web of Science ®Google Scholar
• Simpson R. W., Hauser R. E. Influence of lipids on the viral phenotype. II. Interaction of myxoviruses and their lipid constituents with phospholipase. Virology 1966; 30: 684
   PubMed Web of Science ®Google Scholar
• Friedman R. M., Pastan I. Nature and function of the structural phospholipids of an arbovirus (SFV. J. Mol. Biol. 1969; 40: 107
   PubMed Web of Science ®Google Scholar
• Cartwright B., Smale C. J., Brown F. Surface structure of vesicular stomatitis viru. J. Gen. Virol. 1969; 5: 1
   PubMed Web of Science ®Google Scholar
• Glaser M., Simpkins H., Singer S. J., Sheetz M., Chan S. I. On the interactions of lipids and proteins in the red blood cell membran. Proc. Natl. Acad. Sci. U.S.A. 1970; 65: 721
   PubMed Web of Science ®Google Scholar
• Viola E., Strinna E., Bragadin M., Azzone G. F. Functional and structural changes induced by phospholipase C in intact mitochondria and submitochondrial particle. Biochim. Biophys. Acta 1976; 433: 318
   Google Scholar
• Prasad R., Kalra V. K., Brodie A. F. Effect of phospholipase A on the structure and functions of membrane vesicles from Mycobacterium phlei. J. Biol. Chem. 1975; 250: 3690
   PubMed Web of Science ®Google Scholar
• Bittman R., Chen W. C., Anderson O. R. Interaction of filipin III and amphotericin B with lecithin-sterol vesicles and cellular membranes. Spectral and electron microscope studie. Biochemistry 1974; 13: 1364
   PubMed Web of Science ®Google Scholar
• Bittman R., Majuk Z., Honig D. S., Compans R. W., Lenard J. Permeability properties of the membrane of vesicular stomatitis virion. Biochim. Biophys. Acta 1976; 433: 63
   PubMedGoogle Scholar
• Majuk Z., Bittman R., Landsberger F. R., Compans R. W. Effects of filipin on the structure and biological activity of enveloped viruse. J. Virol. 1977; 24: 883
   PubMed Web of Science ®Google Scholar
• Wagner R. R., Schnaitman C. A. Proteins of vesicular stomatitis viru. The Biology of Large RNA Viruses, R. D. Burry, B. W. J. Mahy. Academic Press, London 1970; 655
   Google Scholar
• Moore N. F., Patzer E. J., Shaw J. M., Thompson T. E., Wagner R. R. Interaction of vesicular stomatitis virus with lipid vesicles: depletion of cholesterol and effect on virion membrane fluidity and infectivit. J. Virol. 1978; 27: 320
   PubMed Web of Science ®Google Scholar
• Shinitzky M., Inbar M. Microviscosity parameters and protein mobility in biological membrane. Biochim. Biophys. Acta 1976; 433: 133
   PubMed Web of Science ®Google Scholar
• Shattil S. J., Cooper R. A. Membrane microviscosity and human platelet functio. Biochemistry 1976; 15: 4832
   PubMed Web of Science ®Google Scholar
• Luukkonen A., Kääriäïnen L., Renkonen O. Phospholipids of Semliki Forest virus grown in cultured mosquito cell. Biochim. Biophys. Acta 1976; 450: 109
   PubMedGoogle Scholar
• Blough H. A., Weinstein D. B., Lawson D. E. M., Kodicek E. The effect of Vitamin A on myxoviruses. II. Alterations in the lipids of influenza viru. Virology 1967; 33: 459
   PubMed Web of Science ®Google Scholar
• Steinhart W. L., Hogeman C. S., Powanda M. C. Inhibition of the production of infectious herpes simplex virus by clofibrat. Virology 1976; 70: 241
   PubMed Web of Science ®Google Scholar
• Bates S. R., Rothblat G. H. Incorporation of L cell sterols into vesicular stomatitis viru. J. Virol. 1972; 9: 883
   PubMed Web of Science ®Google Scholar
• Mulligan J. J., Lynch R. D., Schneeberger E. E., Geyer R. P. Utilization of exogenous linolenic and oleic acids for plasma membrane phosphoglyceride synthesis in L-fibroblast. Biochim. Biophys. Acta 1977; 470: 92
   PubMedGoogle Scholar
• Saito Y., Chou S. M., Silbert D. F. Animal cell mutants defective in sterol metabolism: a specific selection procedure and partial characterization of defect. Proc. Natl. Acad. Sci. U.S.A. 1977; 74: 3730
   PubMed Web of Science ®Google Scholar
• Walter G., Mudd J. A. lodination of vesicular stomatitis virus with lactoperoxidas. Virology 1973; 52: 574
   PubMed Web of Science ®Google Scholar
• Moore N. F., Kelley J. M., Wagner R. R. Envelope proteins of vesicular stomatitis virions: accessibility to iodinatio. Virology 1974; 61: 292
   PubMed Web of Science ®Google Scholar
• Eger R., Compans R. W., Rifkin D. B. The organization of the proteins of vesicular stomatitis virions: labeling with pyridoxal phosphat. Virology 1975; 66: 610
   PubMed Web of Science ®Google Scholar
• McSharry J. J. The effect of chemical and physical treatments on the lactoperoxidase catalyzed iodination of vesicular stomatitis viru. Virology 1977; 83: 482
   PubMed Web of Science ®Google Scholar
• Sefton B. M., Wickus G. G., Burge B. W. Enzymatic iodination of Sindbis virus protei. J. Virol. 1973; 11: 730
   PubMed Web of Science ®Google Scholar
• McCarthy M., Harrison S. C. Glycosidase susceptibility, a probe for the distribution of glycoprotein oligosaccharides in Sindbis viru. J. Virol. 1977; 23: 61
   PubMed Web of Science ®Google Scholar
• Luukkonen A., Gahmberg C. G., Renkonen O. Surface labeling of Semliki Forest virus glycoproteins using galactose oxidase. Exposure of E3-glycoprotei. Virology 1977; 76: 55
   PubMed Web of Science ®Google Scholar
• Stanly P., Haslam E. A. The polypeptides of influenza virus. V. Localization of polypeptides in the virion by iodination technique. Virology 1971; 46: 764
   PubMed Web of Science ®Google Scholar
• McLellan W. L., August J. T. Analysis of the envelope of Rauscher murine oncornaviruses: in vitro labeling of glycopeptide. J. Virol. 1976; 20: 627
   PubMed Web of Science ®Google Scholar
• Famulari N. G., Buchhagen D. L., Klenk H.-D., Fleissner E. Presence of murine leukemia virus envelope proteins gp70 and p15E in a common polyprotein of infected cell. J. Virol. 1976; 20: 501
   PubMed Web of Science ®Google Scholar
• Witte O. N., Weissman I. L., Kaplan H. S. Structural characteristics of some murine oncornaviruses studied by lactoperoxidase iodinatio. Proc. Natl. Acad. Sci. U.S.A. 1973; 70: 36
   PubMed Web of Science ®Google Scholar
• Schloemer R. H., Schlom J., Schochetman G., Kimball P., Wagner R. R. Sialylation of glycoproteins of murine mammary tumor virus, murine leukemia virus, and Mason-Pfizer monkey viru. J. Virol. 1976; 18: 804
   PubMed Web of Science ®Google Scholar
• McSharry J. J., Compans R. W., Choppin P. W. Proteins of vesicular stomatitis virus and of phenotypically mixed vesicular stomatitis virus-simian virus 5 virion. J. Virol. 1971; 8: 722
   PubMed Web of Science ®Google Scholar
• Bussereau F., Cartwright B., Doel T. R., Brown F. A comparative study of the surface projections of different strains of vesicular stomatitis viru. J. Gen. Virol. 1975; 29: 189
   PubMed Web of Science ®Google Scholar
• Compans R. W., Klenk H.-D., Caliguiri L. A., Choppin P. W. Influenza virus proteins. I. Analysis of polypeptides of the virion and identification of spike glycoprotein. Virology 1970; 42: 880
   PubMed Web of Science ®Google Scholar
• Schulze I. T. The structure of influenza virus. I. The polypeptides of the virio. Virology 1970; 42: 890
   PubMed Web of Science ®Google Scholar
• Chen G., Compans R. W., Choppin P. W. Parainfluenza virus surface projections. Glycoproteins with hemagglutinin and neuraminidase activitie. J. Gen. Virol. 1971; 11: 53
   PubMed Web of Science ®Google Scholar
• Gahmberg C. G., Utermann G., Simons K. The membrane proteins of Semliki Forest virus have a hydrophobic part attached to the viral membran. FEBS Lett. 1972; 28: 179
   PubMed Web of Science ®Google Scholar
• Compans R. W. Location of the glycoprotein in the membrane of Sindbis viru. Nature (London) New Biol. 1971; 229: 114
   PubMedGoogle Scholar
• Rifkin D. B., Compans R. W. Identification of the spike proteins of Rous sarcoma viru. Virology 1971; 46: 485
   PubMed Web of Science ®Google Scholar
• Obijeski J. F., Bishop D. H. L., Murphy F. A., Palmer E. L. Structural proteins of La Cross viru. J. Virol. 1976; 19: 985
   PubMed Web of Science ®Google Scholar
• Bächi T., Gierhard W., Lindenmann J., Mühlethaier K. Morphogenesis of influenza A virus in Ehrlich ascites tumor cells as revealed by thin-sectioning and freeze-etchin. J. Virol. 1969; 4: 769
   PubMed Web of Science ®Google Scholar
• Apostolov K., Flewett T. H. Further observations on the structure of influenza viruses A and . J. Gen. Virol. 1969; 4: 365
   PubMed Web of Science ®Google Scholar
• Compans R. W., Dimmock N. J. An electron microscopic study of single cycle infection of chick embryo fibroblasts by influenza viru. Virology 1969; 39: 499
   PubMed Web of Science ®Google Scholar
• Kendal A. P., Apostolov K., Belyavin G. The effect of protease treatment on the morphology of influenza A, B and C viruse. J. Gen. Virol. 1969; 5: 141
   PubMed Web of Science ®Google Scholar
• Schulze I. T. The structure of influenza virus. 11. A model based on the morphology and composition of subviral particle. Virology 1972; 47: 181
   PubMed Web of Science ®Google Scholar
• Kelley J. M., Emerson S. U., Wagner R. R. The glycoprotein of vesicular stomatitis virus is the antigen that gives rise to and reacts with neutralizing antibod. J. Virol. 1972; 10: 1231
   PubMedGoogle Scholar
• Dietzschold B., Schneider L. G., Cox J. H. Serological characterization of the three major proteins of vesicular stomatitis viru. J. Virol. 1974; 14: 1
   PubMed Web of Science ®Google Scholar
• Cartwright B., Talbot P., Brown F. The proteins of biologically active subunits of vesicular stomatitis viru. J. Gen. Virol. 1970; 7: 267
   PubMed Web of Science ®Google Scholar
• Emerson S. U., Wagner R. R. Dissociation and reconsitution of the transcriptase and template activities of vesicular stomatitis B and T virion. J. Virol. 1972; 10: 297
   PubMed Web of Science ®Google Scholar
• McAllister P. E., Wagner R. R. Structural proteins of two salmonid rhabdoviruse. J. Virol. 1975; 15: 733
   PubMed Web of Science ®Google Scholar
• Shimizu K., Hosaka Y., Shimizu Y. K. Solubilization of envelopes of HVJ (Sendai virus) with akalai-Emasol treatment and reassembly of envelope particles with removal of the detergen. J. Virol. 1972; 9: 842
   PubMed Web of Science ®Google Scholar
• Shimizu K., Ishida N. The smallest protein of Sendai virus: its candidate function of binding nucleocapsid to envelop. Virology 1975; 67: 427
   Web of Science ®Google Scholar
• McSharry J. J., Compans R. W., Lackland H., Choppin P. W. Isolation and characterization of the nonglycosylated membrane protein and a nucleocapsid complex from the paramyxovirus SV. Virology 1975; 67: 365
   PubMed Web of Science ®Google Scholar
• Hewitt J. A., Nermut M. V. A morphological study of the M protein of Sendai viru. J. Gen. Virol. 1977; 84: 127
   Google Scholar
• Yoshida T., Nagai Y., Yoshi S., Maeno K., Matsumoto T., Hoshino M. Membrane (M) protein of HVJ (Sendai virus): its role in virus assembl. Virology 1976; 71: 143
   PubMed Web of Science ®Google Scholar
• Mountcastle W. E., Choppin P. W. A comparison of the polypeptides of four measles virus strain. Virology 1977; 78: 463
   PubMed Web of Science ®Google Scholar
• Lamb R. A., Many B. W. J., Choppin P. W. The synthesis of Sendai virus polypeptides in infected cell. Virology 1976; 69: 116
   PubMed Web of Science ®Google Scholar
• Wang E., Wolf B. A., Lamb R. A., Choppin P. W., Goldberg A. R. The presence of actin in enveloped viruse. Cell Motility, R. Goldman, T. Pollard, J. Rosenbaum. Cold Spring Harbor Laboratory, Cold Spring Harbor, New York 1976; 589
   Google Scholar
• Zavada J. Viral pseudotypes and phenotypic mixin. Arch. Virol. 1976; 50: 1
   PubMed Web of Science ®Google Scholar
• Hecht T. T., Summers D. T. Effect of vesicular stomatitis virus infection on the histocompatibility antigen of L cell. J. Virol. 1972; 10: 578
   PubMed Web of Science ®Google Scholar
• Hecht T. T., Summers D. F. Interactions of vesicular stomatitis virus with murine cell surface antigen. J. Virol. 1976; 19: 833
   PubMed Web of Science ®Google Scholar
• Bubbers J. E., Lilly F. Selective incorporation of H-2 antigenic determinants into Friend virus particle. Nature (London) 1977; 266: 458
   PubMed Web of Science ®Google Scholar
• Strand M., August J. T. Protein kinase and phosophate acceptor proteins in Rauscher murine leukemia viru. Nature (London) New Biol. 1971; 233: 137
   PubMedGoogle Scholar
• Imblum R. L., Wagner R. R. Protein kinase and phosphoproteins of vesicular stomatitis viru. J. Virol. 1974; 13: 113
   PubMed Web of Science ®Google Scholar
• Mover S. A., Summer D. F. Phosphorylation of vesicular stomatitis virus in vivo and, in vitr. J. Virol. 1974; 13: 455
   PubMed Web of Science ®Google Scholar
• Mizutani S., Temin H. M. Enzymes and nucleotides in virions of Rous sarcoma viru. J. Virol. 1971; 8: 409
   PubMed Web of Science ®Google Scholar
• Sturman L. S. Characterization of a coronavirus structural proteins: effects of preparative conditions on the migration of protein in polyacrylamide gel. Virology 1977; 77: 637
   PubMed Web of Science ®Google Scholar
• Furthmayr H., Marchesi V. T. Subunit structure of human erythrocyte glycophorin . Biochemistry 1976; 15: 1137
   PubMed Web of Science ®Google Scholar
• Capaldi R. A. Membrane Proteins and their Interaction with Lipids. Marcel Dekker, Inc., New York 1977
   Google Scholar
• Skehel J. J., Waterfield M. D. Studies on the primary structure of the influenza virus glycoprotei. Proc. Natl. Acad. Sci. U.S.A. 1975; 72: 93
   PubMed Web of Science ®Google Scholar
• Gething M. J., White J. M., Waterfield M. D. Purification of the fusion protein of Sendai virus: analysis of the NH2-terminal sequence generated by precursor activatio. Proc. Natl. Acad. Sci. U.S.A. 1978; 75: 2737
   PubMed Web of Science ®Google Scholar
• Rothman J. E., Lodish H. F. Synchronized transmembrane insertion and glycosylation of a nascent membrane protei. Nature (London) 1977; 269: 775
   PubMed Web of Science ®Google Scholar
• Cohen G. H., Atkinson P. H., Summers D. F. Interaction of vesicular stomatitis virus structural proteins with HeLa plasma membran. Nature (London), New Biol. 1971; 231: 121
   PubMedGoogle Scholar
• Wagner R. R., Kiley M. P., Snyder R. M., Schnaitman C. A. Cytoplasmic compartmentalization of the proteins and RNA of vesicular stomatitis viru. J. Virol. 1972; 9: 672
   PubMed Web of Science ®Google Scholar
• David A. E. Assembly of the vesicular stomatitis envelope: incorporation of viral polypeptides into the host plasma membran. J. Mol. Biol. 1973; 76: 135
   PubMed Web of Science ®Google Scholar
• Morrison T. G., Lodish H. F. Site of synthesis of membrane and non-membrane proteins of vesicular stomatitis viru. J. Biol. Chem. 1975; 250: 6955
   PubMed Web of Science ®Google Scholar
• Atkinson P. H., Moyer S. A., Summers D. F. Assembly of vesicular stomatitis virus glycoprotein and matrix protein into HeLa cell plasma membrane. J. Mol. Biol. 1976; 102: 613
   PubMed Web of Science ®Google Scholar
• Hunt L. A., Summers D. F. Association of vesicular stomatitis virus proteins with HeLa cell membranes and released viru. J. Virol. 1976; 20: 637
   PubMed Web of Science ®Google Scholar
• David A. E. Assembly of the vesicular stomatitis virus envelope: transfer of viral polypeptides from polysomes to cellular membrane. Virology 1977; 76: 98
   PubMed Web of Science ®Google Scholar
• Knipe D. M., Baltimore D., Lodish H. F. Separate pathways of maturation of the major structural proteins of vesicular stomatitis viru. J. Virol. 1977; 21: 1128
   PubMed Web of Science ®Google Scholar
• Knipe D. M., Lodish H. F., Baltimore D. Localization of two cellular forms of the vesicular stomatitis viral glycoprotei. J. Virol. 1977; 21: 1121
   PubMed Web of Science ®Google Scholar
• Morrison T. G., McQuain C. O. Assembly of viral membranes: nature of the association of vesicular stomatitis virus proteins to membrane. J. Virol. 1978; 26: 115
   PubMed Web of Science ®Google Scholar
• Lafay F. Envelope proteins of vesicular stomatitis virus: effect of temperature-sensitive mutants in complementation groups III and . J. Virol. 1974; 14: 1220
   PubMed Web of Science ®Google Scholar
• Knipe D. M., Baltimore D., Lodish H. F. Maturation of viral proteins in cells infected with temperature-sensitive mutants of vesicular stomatitis viru. J. Virol. 1977; 21: 1149
   PubMed Web of Science ®Google Scholar
• Morrison T. G., McQuain C. O., Simpson D. Assembly of viral membranes: maturation of the vesicular stomatitis virus glycoprotein in the presence of tunicamyci. J. Virol. 1978; 28: 368
   PubMed Web of Science ®Google Scholar
• Katz F., Rothman J. E., Lingappa V. R., Blobel G., Lodish H. F. Membrane assembly in vitro: synthesis, glycosylation and asymmetric insertion of a transmembrane protei. Proc. Natl. Acad. Sci. U.S.A. 1977; 74: 3278
   PubMed Web of Science ®Google Scholar
• Toneguzzo F., Ghosh H. P. Synthesis and glycosylation in vitro of glycoprotein of vesicular stomatitis viru. Proc. Natl. Acad. Sci. U.S.A. 1977; 74: 1516
   PubMed Web of Science ®Google Scholar
• Toneguzzo F., Ghosh H. P. In vitro synthesis of vesicular stomatitis virus membrane glycoprotein and insertion into membrane. Proc. Natl. Acad. Sci. U.S.A. 1978; 75: 715
   PubMed Web of Science ®Google Scholar
• Blobel G., Doberstein B. Transfer of proteins across membranes. I. Presence of proteolytically processed and unprocessed nascent immunoglobulin light chains on membrane-bound ribosomes of murine myelom. J. Cell Biol. 1975; 67: 835
   PubMed Web of Science ®Google Scholar
• Katz F. N., Rothman J. E., Knipe D. M., Lodish H. F. Membrane assembly: synthesis and intracellular processing of the vesicular stomatitis virus glycoprotei. J. Supramol. Struct. 1977; 7: 353
   PubMedGoogle Scholar
• Atkinson P. H. Glycoprotein and protein precursors to plasma membrane in vesicular stomatitis virus infected HeLa cell. J. Supramol. Struct. 1977; 8: 525
   Google Scholar
• Schlesinger M. J., Schlesinger S., Burge B. W. Identification of a second glycoprotein in Sindbis viru. Virology 1972; 47: 539
   PubMed Web of Science ®Google Scholar
• Sefton B. M., Keegstra K. Glycoproteins of Sindbis virus: preliminary characterization of the oligosaccharide. J. Virol. 1974; 14: 522
   PubMed Web of Science ®Google Scholar
• Burge B. W., Huang A. S. Comparison of membrane protein glycopeptides of Sindbis virus and vesicular stomatitis viru. J. Virol. 1970; 6: 176
   PubMed Web of Science ®Google Scholar
• Burge B. W., Strauss J. H. Glycopeptides of the membrane glycoprotein of Sindbis viru. J. Mol. Biol. 1970; 47: 449
   PubMedGoogle Scholar
• Keegstra K., Sefton B., Burke D. Sindbis virus glycoproteins: effect of the host cell on the oligosaccharide. J. Virol. 1975; 16: 613
   PubMed Web of Science ®Google Scholar
• Burke D. J., Keegstra K. Purification and composition of the proteins from Sindbis virus grown in chick and BHK cell. J. Virol. 1977; 20: 676
   Web of Science ®Google Scholar
• Etchison J. R., Holland J. J. Carbohydrate composition of the membrane glycoprotein of vesicular stomatitis virus grown in four mammalian cell line. Proc. Natl. Acad. Sci. U.S.A. 1974; 71: 4011
   PubMed Web of Science ®Google Scholar
• Moyer S. A., Summers D. F. Vesicular stomatitis virus envelope glycoprotein alterations induced by host cell transformatio. Cell 1974; 7: 63
   Google Scholar
• Moyer S. A., Tsang J. M., Athinson P. H., Summers D. F. Oligosaccharide moieties of the glycoprotein of vesicular stomatitis viru. J. Virol 1976; 18: 167
   PubMed Web of Science ®Google Scholar
• Robertson J. S., Etchison J. R., Summers D. F. Glycosylation sites of vesicular stomatitis virus glycoprotei. J. Virol. 1976; 19: 871
   PubMed Web of Science ®Google Scholar
• Etchison J. R., Robertson J. S., Summers D. F. Partial structural analysis of the oligosaccharide moieties of the vesicular stomatitis virus glycoprotein by sequential chemical and enzymatic degradatio. Virology 1977; 78: 375
   PubMed Web of Science ®Google Scholar
• Emerson S. U. Vesicular stomatitis virus: structure and function of virion component. Current Top. Microbiol. Immunol. 1976; 73: 1
   PubMedGoogle Scholar
• Dietzschold B. Oligosaccharides of the glycoprotein of rabies viru. J. Virol. 1977; 23: 286
   PubMed Web of Science ®Google Scholar
• Sefton B. M. Virus-dependent glycosylatio. J. Virol. 1976; 17: 85
   Web of Science ®Google Scholar
• Keegstra K., Burke D. Comparision of the carbohydrate of Sindbis virus glycoproteins with the carbohydrate of host glycoprotein. J. Supramol. Struct. 1977; 7: 371
   PubMedGoogle Scholar
• Schwarz R. T., Schmidt M. F. G., Anwer U., Klenk H.-D. Carbohydrates of influenza virus. I. Glycopeptides derived from viral glycoproteins after labeling with radioactive sugar. J. Virol. 1977; 23: 217
   PubMed Web of Science ®Google Scholar
• Nakamura K., Compans R. W. Glycopeptide components of influenza viral glycoprotei. Virology 1978; 86: 432
   PubMed Web of Science ®Google Scholar
• Compans R. W., Pinter A. Incorporation of sulfate into influenza glycoprotein. Virology 1975; 66: 151
   PubMed Web of Science ®Google Scholar
• Nakamura K., Compans R. W. The cellular site of sulfation of influenza viral glycoprotein. Virology 1977; 79: 381
   PubMed Web of Science ®Google Scholar
• Kaplan A. S., Ben-Porat T. Synthesis of proteins in cells infected with herpesvirus. XI. Sulfated, structural glycoprotei. Virology 1976; 70: 561
   PubMed Web of Science ®Google Scholar
• Kornfeld R., Kornfeld S. Comparative aspects of glycoprotein structur. Annu. Rev. Biochem. 1976; 45: 217
   PubMed Web of Science ®Google Scholar
• Waechter C. J., Lennarz W. J. The role of polyprenol-linked sugars in glycoprotein synthesi. Annu. Rev. Biochem. 1976; 45: 95
   PubMed Web of Science ®Google Scholar
• Robbins P. W., Hubbard S. C., Turco S. J., Wirth D. F. Proposal for a common oligosaccharide intermediate in the synthesis of membrane glycoprotein. Cell 1977; 12: 893
   PubMed Web of Science ®Google Scholar
• Reading C. L., Penhoet E. E., Ballou C. E. Carbohydrate structure of vesicular stomatitis virus glycoprotei. J. Biol. Chem. 1978; 253: 5600
   PubMed Web of Science ®Google Scholar
• Klenk H.-D., Scholtissek C., Rott R. Inhibition of glycoprotein biosynthesis of influenza virus by D-glucosamine and 2-deoxy-D-glucos. Virology 1972; 49: 723
   PubMed Web of Science ®Google Scholar
• Compans R. W., Meier-Ewart H., Palese P. Assembly of lipid-containing viruse. J. Supramol. Struct. 1974; 2: 496
   PubMedGoogle Scholar
• Takatsuki A., Kohno K., Tamura G. Inhibition of biosynthesis of polyisoprenol sugars in chick embryo microsomes by tunicamyci. Agric. Biol. Chem. 1975; 39: 2089
   Web of Science ®Google Scholar
• Tkacz J. S., Lampen J. O. Tunicamycin inhibition of polyisoprenol N-acetylglucosaminyl pyrophosphate formation in calf liver microsome. Biochem. Biophys. Res. Commun. 1975; 65: 248
   PubMed Web of Science ®Google Scholar
• Leavitt R., Schlesinger S., Kornfeld S. Tunicamycin inhibits glycosylation and multiplication of Sindbis and vesicular stomatitis viruse. J. Virol. 1977; 21: 375
   PubMed Web of Science ®Google Scholar
• Gibson R., Leavitt R., Kornfeld S., Schlesinger S. Synthesis and infectivity of vesicular stomatitis virus containing nonglycosylated G protei. Cell 1978; 13: 671
   PubMed Web of Science ®Google Scholar
• Nakamura K., Compans R. W. Effects of glucosamine, 2-deoxyglucose, and tunicamycin on glycosylation, sulfation, and assembly of influenza viral protein. Virology 1978; 84: 303
   PubMed Web of Science ®Google Scholar
• Garoff H., Schwarz R. T. Glycosylation is not necessary for membrane insertion and cleavage of Semliki Forest virus membrane protein. Nature (London) 1978; 274: 487
   PubMed Web of Science ®Google Scholar
• Schloemer R. H., Wagner R. R. Sialoglycoprotein of vesicular stomatitis virus: role of the neuraminic acid in infectio. J. Virol. 1974; 14: 270
   PubMed Web of Science ®Google Scholar
• Dore-Duffy P., Howe C. N-acetylneuraminic acid in measles viru. Proc. Soc. Exp. Biol. Med. 1978; 157: 622
   PubMed Web of Science ®Google Scholar
• Cartwright B., Brown F. Role of sialic acid in infection with vesicular stomatitis viru. J. Gen. Virol. 1977; 35: 197
   PubMed Web of Science ®Google Scholar
• McSharry J. J., Ledda C. A., Freeman H. J., Choppin P. W. Biological properties of the VSV glycoprotein. II. Effects of the host cell and of the glycoprotein carbohydrate composition on hemagglutinatio. Virology 1978; 84: 183
   PubMed Web of Science ®Google Scholar
• Robertson M. A., Etchison J. R., Robertson J. S., Summers D. F., Stanley P. Specific changes in the oligosaccharide moities of VSV grown in different lectin-resistant CHO cell. Cell 1978; 13: 515
   PubMed Web of Science ®Google Scholar
• August M. J., Harter D. H., Compans R. W. Characterization of Visna virus envelope neuraminic aci. J. Virol. 1977; 22: 832
   PubMed Web of Science ®Google Scholar
• Stollar V., Stollar B. D., Koo R., Harrap K. A., Schlesinger R. W. Sialic acid content of Sindbis virus from vertebrate and mosquito cell. Virology 1976; 69: 104
   PubMed Web of Science ®Google Scholar
• Collins J. K., Knight C. A. Removal of carbohydrate from influenza A virus and its hemagglutinin and the effect on biological activitie. J. Virol. 1978; 27: 164
   PubMed Web of Science ®Google Scholar
• Bolognesi D. P., Collins J. J., Leis J. P., Moenning V., Schäfer W., Atkinson P. H. Role of carbohydrate in determining the immunological properties of the major glycoprotein (gp71) of Friend leukemia viru. J. Virol. 1975; 16: 1453
   PubMed Web of Science ®Google Scholar
• Schäfer W., Fischinger P. J., Collins J. J., Bolognesi D. P. Role of carbohydrate in biological functions of Friend murine leukemia virus gp7. J. Virol. 1977; 21: 35
   PubMed Web of Science ®Google Scholar
• Van Eldik L. J., Paulson J. C., Green R. W., Smith R. E. The influence of carbohydrate on the antigenicity of the envelope glycoprotein of avian myeloblastosis virus and B, avian sarcoma viru. Virology 1978; 86: 193
   PubMed Web of Science ®Google Scholar
• Lazarowitz S. G., Compans R. W., Choppin P. W. Influenza virus structural and non-structural proteins in infected cells and their plasma membrane. Virology 1971; 46: 830
   PubMed Web of Science ®Google Scholar
• Lazarowitz S. G., Compans R. W., Choppin P. W. Proteolytic cleavage of the hemagglutinin polypeptides of influenza virus. Function of the uncleaved polypeptide H. Virology 1973; 52: 199
   PubMed Web of Science ®Google Scholar
• Skehel J. J. Polypeptide synthesis in influenza virus-infected cell. Virology 1972; 49: 23
   PubMed Web of Science ®Google Scholar
• Stanley P., Gandhi S. S., White D. O. The polypeptides of influenza virus. VII. Synthesis of the hemagglutini. Virology 1973; 53: 92
   PubMed Web of Science ®Google Scholar
• Laver R. Separation of two polypeptide chains from the hemagglutinin subunit of influenza viru. Virology 1971; 45: 275
   PubMed Web of Science ®Google Scholar
• Skehel J. J., Schild G. The polypeptide composition of influenza A viruse. Virology 1971; 44: 396
   PubMed Web of Science ®Google Scholar
• Klenk H.-D., Rott R., Orlich M., Blödorn J. Activation of influenza A viruses by trypsin treatmen. Virology 1975; 68: 426
   PubMed Web of Science ®Google Scholar
• Lazarowitz S. G., Choppin P. W. Enhancement of the infectivity of influenza A and B viruses by proteolytic cleavage of the hemagglutinin polypeptid. Virology 1975; 68: 440
   PubMed Web of Science ®Google Scholar
• Homma M. Trypsin action on the growth of Sendai virus in tissue culture. I. Restoration of the infectivity for L cells by direct action of trypsin on L cell-borne Sendai viru. J. Virol 1971; 8: 619
   PubMed Web of Science ®Google Scholar
• Homma M., Ohuchi M. Trypsin action on the growth of Sendai virus in tissue culture cells. III. Structural difference of Sendai viruses grown in eggs and tissue culture cell. J. Virol. 1973; 12: 1457
   PubMed Web of Science ®Google Scholar
• Scheid A., Choppin P. W. Identification of the biological activities of paramyxovirus glycoproteins. Activation of cell fusion, hemolysis, and infectivity by proteolytic cleavage of an inactive precursor protein of Sendai viru. Virology 1974; 57: 475
   PubMed Web of Science ®Google Scholar
• Ohuchi M., Homma M. Trypsin action on the growth of Sendai virus in tissue culture cells. IV. Evidence for activation of Sendai virus by cleavage of a glycoprotei. J. Virol. 1976; 18: 1147
   PubMed Web of Science ®Google Scholar
• Scheid A., Choppin P. W. Two disulfide-linked polypeptide chains constitute the active F protein of paramyxoviruse. Virology 1977; 80: 54
   PubMed Web of Science ®Google Scholar
• Nagai Y., Klenk H.-D., Rott R. Proteolytic cleavage of the viral glycoprotein and its significance for the virulence of Newcastle disease viru. Virology 1976; 72: 494
   PubMed Web of Science ®Google Scholar
• Nagai Y., Klenk H.-D. Activation of precursors to both glycoproteins of Newcastle disease virus by proteolytic cleavag. Virology 1977; 77: 125
   PubMed Web of Science ®Google Scholar
• Schlesinger S., Schlesinger M. J. Formation of Sindbis virus proteins: identification of a precursor for one of the envelope protein. J. Virol. 1972; 10: 925
   PubMed Web of Science ®Google Scholar
• Simons K., Keranen S., Kaariainen L. Identification of a precursor for one of the Semliki Forest virus membrane protein. FEBS Lett. 1973; 29: 87
   PubMed Web of Science ®Google Scholar
• Dickson C., Puma J. P., Nandi S. Identification of a precursor protein to the major glycoproteins of mouse mammary tumor viru. J. Virol. 1976; 17: 275
   Web of Science ®Google Scholar
• Laver W. G., Valentine R. C. Morphology of the isolated hemagglutinin and neuraminidase subunits of influenza viru. Virology 1969; 38: 105
   PubMed Web of Science ®Google Scholar
• Brand C. M., Skehel J. J. Crystalline antigen from the influenza virus envelop. Nature (London), New Biol. 1972; 238: 145
   PubMedGoogle Scholar
• Laver W. G. The polypeptides of influenza viruse. Adv. Virus Res. 1973; 18: 57
   Google Scholar
• Wiley D. C., Skehel J. J., Waterfield M. Evidence from studies with a crosslinking reagent that the hemagglutinin of influenza virus is a trime. Virology 1977; 79: 446
   PubMed Web of Science ®Google Scholar
• Wrigley N. G., Skehel J. J., Charlwood P. A., Brand C. M. The size and shape of influenza virus neuraminidas. Virology 1973; 51: 525
   PubMed Web of Science ®Google Scholar
• Kendal A. P., Echert E. A. The preparation and properties of14C-carboxyaminomethylated subunits from A2/1957 influenza neuraminidas. Biochim. Biophys. Acta 1972; 258: 484
   PubMedGoogle Scholar
• Bucher D. J., Kilbourne E. D. A2(N2) neuraminidase of the X-7 influenza virus recombinant: determination of the molecular size and subunit composition of the active uni. J. Virol. 1972; 10: 60
   PubMed Web of Science ®Google Scholar
• Scheid A., Caliguiri L. A., Compans R. W., Choppin P. W. Isolation of paramyxovirus glycoproteins. Association of both hemagglutinating and neuraminidase activities with the larger SV5 glycoprotei. Virology 1972; 50: 640
   PubMed Web of Science ®Google Scholar
• Scheid A., Choppin P. W. Isolation and purification of the envelope proteins of Newcastle disease viru. J. Virol. 1973; 11: 263
   PubMed Web of Science ®Google Scholar
• Ozawa M., Asano A., Okada Y. Importance of interpeptide disulfide bond in a viral glycoprotein with hemagglutination and neuraminidase activitie. FEBS Lett. 1976; 70: 145
   PubMed Web of Science ®Google Scholar
• Moore N. F., Burke D. C. Characterization of the structural proteins of different strains of Newcastle disease viru. J. Gen. Virol. 1974; 25: 275
   PubMed Web of Science ®Google Scholar
• Moore N. F., Kelly D. C. Sendai virus structural proteins: analysis of polypeptides linked with disulfide bond. Intervirology 1973; 2: 128/74
   Web of Science ®Google Scholar
• Hardwick J. M., Bussell R. H. Glycoproteins of measles virus under reducing and nonreducing condition. J. Virol. 1978; 25: 687
   PubMedGoogle Scholar
• Simons K., Helenius A., Garoff H. Solubilization of the membrane proteins from Semliki Forest virus with Triton X-10. J. Mol. Biol. 1973; 80: 119
   PubMed Web of Science ®Google Scholar
• Garoff H. Crosslinking of the spike glycoproteins in Semliki Forest virus with dimethylsuberimidat. Virology 1974; 62: 385
   PubMed Web of Science ®Google Scholar
• Jones K. J., Scupham R. K., Pferl J. A., Wan K., Sagik B. P., Bose H. R. Interaction of Sindbis virus glycoproteins during morphogenesi. J. Virol. 1977; 21: 778
   PubMed Web of Science ®Google Scholar
• Leamnson R. N., Halpern M. S. Subunit structure of the glycoprotein complex of avian tumor viru. J. Virol. 1976; 18: 956
   PubMed Web of Science ®Google Scholar
• Montelaro R. C., Sullivan S. J., Bolognesi D. P. An analysis of type-C retrovirus polypeptides and their associations in the virion. Virology 1978; 84: 19
   PubMed Web of Science ®Google Scholar
• Pinter A., Fleissner E. The presence of disulfidelinked gp70-p15(E) complexes in AKR murine leukemia viru. Virology 1977; 83: 417
   PubMed Web of Science ®Google Scholar
• England J. M., Bolognesi D. P., Dietzschold B., Halpern M. S. Evidence that a precursor glycoprotein is cleaved to yield the major glycoprotein of avian tumor viru. J. Virol. 1977; 21: 810
   PubMed Web of Science ®Google Scholar
• Brown D. T., Waite M. R. F., Pfefferkorn E. R. Morphology and morphogenesis of Sindbis virus as seen with freeze-etching technique. J. Virol. 1972; 10: 524
   PubMed Web of Science ®Google Scholar
• Brown D. T., Riedel B. Morphogenesis of vesicular stomatitis virus: electron microscopic observations with freeze-fracture technique. J. Virol. 1977; 21: 601
   PubMed Web of Science ®Google Scholar
• Deamer D. W. The relation of membrane ultrastructure to membrane functio. Mammalian Cell Membranes, G. A. Jamieson, D. M. Robinson. Butterworths, London 1977; Vol. 4: 1
   Google Scholar
• Garoff H., Simons K. Location of the spike glycoproteins in the Semliki Forest virus membran. Proc. Natl. Acad. Sci. U.S.A. 1977; 71: 3988
   Google Scholar
• Garoff H. Crosslinking of the spike glycoproteins in Semiliki Forest virus with dimethylsuberimidat. Virology 1974; 62: 385
   PubMed Web of Science ®Google Scholar
• von Bondsdorff G. H., Harrison S. C. Sindbis virus proteins form a regular icosahedral surface lattic. J. Virol. 1975; 16: 141
   PubMed Web of Science ®Google Scholar
• Dubovi E. J., Wagner R. R., unpublished data
   Google Scholar
• Richardson C. D., Vance D. E. Chemical crosslinking of the proteins of Semliki Forest virus: studies with virus particles and plasma membranes from BHK-21 cells treated with colchicine or dibucain. J. Virol. 1978; 28: 193
   PubMed Web of Science ®Google Scholar
• Dubovi E. J., Wagner R. R. Spatial relationships of the proteins of vesicular stomatitis virus: induction of reversible oligomers by cleavable protein cross-linkers and oxidatio. J. Virol. 1977; 22: 500
   PubMed Web of Science ®Google Scholar
• Miyakawa T., Takemoto L. J., Fox C. F. Supramolecular organization of proteins in Newcastle disease viru. Animal Virology, A. S. Huang, D. Baltimore, C. F. Fox. Academic Press, New York 1976; 465
   Google Scholar
• Howe C., Lee L. T. Virus-erythrocyte interaction. Adv. Virus Res. 1972; 17: 1
   PubMedGoogle Scholar
• Bächi T., Deas J. E., Howe C. Virus-erythrocyte membrane interaction. Virus Infection and the Cell Surface, G. Poste, G. L. Nicolson. North-Holland, Amsterdam 1977; 83
   Google Scholar
• Poste G., Allison A. C. Membrane fusio. Biochim. Biophys. Acta 1973; 300: 421
   PubMed Web of Science ®Google Scholar
• Shotton D. Freeze-fracture view of membrane fusio. Nature (London) 1978; 272: 16
   Web of Science ®Google Scholar
• Papahadjopoulos D., Poste G., Schaeffer B. E. Fusion of mammalian cells by unilamellar lipid vesicles: influence of lipid surface charge, fluidity and cholestero. Biochim. Biophys. Acta 1973; 323: 23
   PubMed Web of Science ®Google Scholar
• Lucy A. J. The fusion of biological membrane. Nature (London) 1970; 227: 815
   PubMed Web of Science ®Google Scholar
• Pagano R. E., Huang L. Interaction of phospholipid vesicles with cultured mammalian cells. II. Studies of mechanis. J. Cell Biol. 1975; 67: 49
   PubMed Web of Science ®Google Scholar
• Weinstein J. N., Yoshikami S., Henkart P., Blumenthal R., Hagins W. A. Liposome-cell interaction: transfer and intracellular release of a trapped fluorescent marke. Science 1977; 195: 489
   PubMed Web of Science ®Google Scholar
• Shimizu Y. K., Shimizu K., Ishida N., Homma M. On the study of Sendai virus hemolysis. II. Morphological study of envelope fusion and hemolysi. Virology 1976; 71: 48
   PubMed Web of Science ®Google Scholar
• Choppin P. W., Klenk H.-D., Compans R. W., Caliguiri L. A. The parainfluenza virus SV5 and its relationship to the cell membran. Perspectives in Virology VII, M. Pollard. Academic Press, New York 1971; 127
   Google Scholar
• Poste G., Reeve P., Alexander D. J., Terry G. Effect of plasma membrane lipid composition on cellular susceptibility to virus-induced cell fusio. J. Gen. Virol 1972; 17: 133
   PubMed Web of Science ®Google Scholar
• Haywood A. M. Characteristics of Sendai virus receptors in a model membran. J. Mol. Biol. 1974; 83: 427
   PubMed Web of Science ®Google Scholar
• Haywood A. M. “Phagocytosis” of Sendai Virus by Model Membrane. J. Gen. Virol. 1975; 29: 63
   PubMed Web of Science ®Google Scholar
• Haywood A. M. Fusion of Sendai viruses with model membrane. J. Mol. Biol. 1974; 87: 625
   PubMed Web of Science ®Google Scholar
• Yamamoto K., Inoue D., Seizuki K. Interaction of paramyxoviruses with erythrocyte membranes modified by concanavalin . Nature (London) 1974; 250: 511
   PubMed Web of Science ®Google Scholar
• Lyles D. S., Landsberger F. R. Virus and lectin agglutination of erythrocytes: spin label study of membrane lipid-protein interaction. Proc. Natl. Acad. Sci. U.S.A. 1976; 73: 3497
   PubMed Web of Science ®Google Scholar
• Levanon A., Kohn A., Inbar M. Increase in lipid fluidity of cellular membranes induced by adsorption of RNA and DNA virion. J. Virol. 1977; 22: 353
   PubMed Web of Science ®Google Scholar
• Maeda T., Asano A., Ohki K., Okada Y., Ohnishi S. A spin-label study on fusion of red blood cells induced by hemagglutinating virus of Japa. Biochemistry 1975; 14: 3736
   PubMed Web of Science ®Google Scholar
• Maeda T., Asano A., Okada Y., Ohnishi S. Transmembrane phospholipid motions induced by F glycoprotein in hemagglutinating virus of Japa. J. Virol. 1977; 21: 232
   PubMed Web of Science ®Google Scholar
• Tanaka K.-I., Ohnishi S.-I. Heterogeneity in the fluidity of intact erythrocyte membrane and its homogenization upon hemolysi. Biochim. Biophys. Acta 1976; 426: 218
   PubMed Web of Science ®Google Scholar
• Nakamura M., Ohnishi S.-I., Kitamura H., Inai S. Membrane fluidity change in erythrocyte induced by complement syste. Biochemistry 1976; 15: 4838
   PubMed Web of Science ®Google Scholar
• Lyles D. S., Landsberger F. R. Sendai virus-induced hemolysis: reduction in heterogeneity of erythrocyte lipid bilayer fluidit. Proc. Natl. Acad. Sci. U.S.A. 1977; 74: 1918
   PubMed Web of Science ®Google Scholar
• Simpson R. W., Hauser R. E., Dales S. Viropexis of vesicular stomatitis virus by L cell. Virology 1969; 17: 285
   Google Scholar
• Heine J. W., Schnaitman C. A. Fusion of vesicular stomatitis virus with cytoplasmic membrane of L cell. J. Virol. 1969; 3: 619
   PubMed Web of Science ®Google Scholar
• Heine J. W., Schnaitman C. A. Entry of vesicular stomatitis virus into L cell. J. Virol. 1971; 8: 786
   PubMed Web of Science ®Google Scholar
• Mason J. T., personal communication
   Google Scholar
• Carroll A. R., personal communication
   Google Scholar
• Patzer E. J., Wagner R. R., unpublished results
   Google Scholar