An analysis of the role of the target membrane on the Gp64-induced fusion pore

Virology

Volumn 253, Issue 1, 1999, Pages 65-76

  Plonsky, Ilya ^a   Cho, Myoung Soon ^a   Oomens, Antonius G P ^b   Blissard, Gary ^b   Zimmerberg, Joshua ^a  

^a EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH AND HUMAN DEVELOPMENT   (United States)

^b United States Department of Agriculture Agricultural Research Service and Boyce Thompson Institute for Plant Research   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

HYBRID PROTEIN; INFLUENZA VIRUS HEMAGGLUTININ;

ANIMAL CELL; ARTICLE; BACULOVIRUS; CELL MEMBRANE CONDUCTANCE; CHANNEL GATING; CONTROLLED STUDY; HOST CELL; LEPIDOPTERA; NONHUMAN; POLYHEDROSIS VIRUS; PRIORITY JOURNAL; PROTEIN AGGREGATION; PROTEIN EXPRESSION; TARGET CELL; VIRUS ENVELOPE;

EID: 0033524323     PISSN: 00426822     EISSN: None     Source Type: Journal    
DOI: 10.1006/viro.1998.9493     Document Type: Article

References (43)

1. Adams, J. R., Goodwin, R. H., and Wilcox, T. A. (1977). Electron microscopic investigations on invasion and replication of insect baculoviruses in vivo and in vitro. biol. Cell. 28, 261-267.
2. Bentz, J. (1992). Intermediates and kinetics of membrane fusion. Biophys. J. 63, 448-459.
3. Blissard, G. W., and Rohrmann, G. F. (1989). Location, sequence, transcriptional mapping, and temporal expression of the gp64 envelope glycoprotein gene of the Orgyia pseudotsugata multicapsid nuclear polyhedrosis virus. Virology 170, 537-555.
4. Blissard, G. W., and Rohrmann, G. F. (1991). Baculovirus gp64 gene expression: Analysis of sequences modulating early transcription and transactivation by IE1. J. Virol. 65, 5820-5827.
5. Blissard, G. W., and Wenz, J. R. (1992). Baculovirus GP64 envelope glycoprotein is sufficient to mediate pH-dependent membrane fusion. J. Virol. 66, 6829-6835.
6. Blumenthal, R., Pak, C. C., Raviv, Y., Krumbiegel, M., Bergelson, L. D., Morris, S. J., and Lowy, R. J. (1995). Transient domains induced by influenza haemagglutinin during membrane fusion. Mol. Membr. Biol. 12, 135-142.
7. Blumenthal, R., Sarkar, D. P., Durell, S. W., Howard, D. E., and Morris, S. J. (1996). Dilation of the influenza hemagglutinin fusion pore revealed by the kinetics of individual cell-cell fusion events. J. Cell biol. 135, 63-71.
8. Breckenridge, L. J., and Almers, W. (1987). Currents through the fusion pore that forms during exocytosis of a secretory vesicle. Nature 328, 814-817.
9. Bundo-Morita, K., Gibson, S., and Lenard, J. (1988). Radiation inactivation analysis of fusion and hemolysis by vesicular stomatitis virus. Virology 163, 622-624.
10. Chernomordik, L., Kozlov, M. M., and Zimmerberg, J. (1995). Lipids in biological membrane fusion. J. Membr. Biol. 146, 1-14.
11. Chernomordik, L. V., Frolov, V. A., Leikina, E., and Zimmerberg, J. (1998). The pathway of membrane fusion catalyzed by influenza hemagglutinin: Restrictions of lipids, hemifusion, and lipidic fusion pore formation. J. Cell Biol. 140, 1369-1382.
12. Chizmadzhev, Y. A., Cohen, F. S., Shcherbakov, A., and Zimmerberg, J. (1995). Membrane mechanics can account for fusion pore dilation in stages. Biophys. J. 69, 2489-2500.
13. Curran, M. J., Cohen, F. S., Chandler, D. E., Munson, P. J., and Zimmerberg, J. (1993). Exocytotic fusion pores exhibit semi-stable states. J. Membr. Biol. 133, 61-75.
14. Danieli, T., Pelletier, S. L., Henis, Y. I., and White, J. M. (1996). Membrane fusion mediated by the influenza virus hemagglutinin requires the concerted action of at least three hemagglutinin trimers. J. Cell Biol. 133, 559-569.
15. Ellens, H., Bentz, J., Mason, D., Zhang, F., and White, J. M. (1990). Fusion of influenza hemagglutinin-expressing fibroblasts with glycophorinbearing liposomes: Role of hemagglutinin surface density. Biochemistry 29, 9697-9707.
16. Gauden Y., Raux, H., Flamand, A., and Ruigrok, R. W. H. (1996). Identification of amino acids controlling the low-pH-induced conformational change of rabies virus glycoprotein. J. Virol. 70, 7371-7378.
17. Hays, W. L., and Winkler, R. L. (1970). "Statistics: Probability, Inference, and Decision," Vol. 2. Holt, Rinehart and Winston, New York.
18. Hink, W. F. (1970). Established insect cell line from the cabbage looper, Trichoplusia ni. Nature 226, 466-467.
19. Kemble, G. W., Danieli, T., and White, J. W. (1994). Lipid-anchored influenza hemagglutinin promotes hemifusion, not complete fusion. Cell 76, 383-391.
20. Kozlov, M. M., Leikin, S. L., Chernomordik, L. V., Markin, V. S, and Chizmadzhev, Y. A. (1989). Stalk mechanism of membrane fusion. Eur. Biophys. J. 17, 121-129.
21. Lanzrein, M., Kasermann, N., Weingart, R., and Kempf, C. (1993). Early events of Semliki Forest virus-induced cell-cell fusion. Virology 196, 541-547.
22. Lindau, M. (1991). Time-resolved capacitance measurements: Monitoring exocytosis in single cells. Q. Rev. Biophys. 24, 75-101.
23. Melikyan, G. B., Jin, H., Lamb, R. A., and Cohen, F. S. (1997). The role of the cytoplasmic tail region in formation and growth of fusion pores. Virology 235, 118-128.
24. Melikyan, G. B., Niles, W. D., and Cohen, F. S. (1993). Influenza virus hemagglutinin-induced cell-planar-bilayer fusion: Quantitative dissection of fusion pore kinetics into stages. J. Gen. Physiol. 102, 1151-1170.
25. Melikyan, G. B., Niles, W. D., and Cohen, F. S. (1995a). The fusion kinetics of influenza hemagglutinin expressing cells to planar bilayer membranes is affected by HA density and host cell surface. J. Gen. Physiol. 106, 783-802.
26. Melikyan, G. B., Niles, W. D., Ratinov, V., Kaharnek, M., Zimmerberg, J., and Cohen, F. S. (1995b). Comparison of transient and successfully open fusion pores connecting hemagglutinin (HA) expressing cells to planar membranes. J. Gen. Physiol. 106, 803-821.
27. Melikyan, G. B., White, J. M., and Cohen, F. S. (1995c). GPI-anchored influenza hemagglutinin induces hemifusion to both red blood cell and planar bilayer membranes. J. Cell Biol. 131, 679-691.
28. Monck, J. R., and Fernandez, J. M. (1992). The exocytotic fusion pore. J. Cell Biol. 119, 1395-1404.
29. Monsma, S. A., and Blissard, G. W. (1995). Identification of a membrane fusion domain and an oligomerization domain in the baculovirus GP64 envelope fusion protein. J. Virol. 69, 2583-2595.
30. Monsma, S. A., Oomens, A. G., and Blissard, G. W. (1996). The GP64 envelope fusion protein is an essential baculovirus protein required for cell-to-cell transmission of infection. J. Virol. 70, 4607-4616.
31. Nanavati, C., Markin, V. S., Oberhauser, A. F., and Fernandez, J. M. (1992). The exocytotic fusion pore modeled as a lipidic pore. Biophys. J. 63, 1118-1132.
32. Neher, E., and Marty, A. (1982). Discrete changes of cell membrane capacitance observed under conditions of enhanced secretion in bovine adrenal chromaffin cells. Proc. Natl. Acad. Sci. USA 79, 6712-6716.
33. Oomens, A. G., Monsma, A., and Blissard, G. W. (1995). The baculovirus GP64 envelope fusion protein: Synthesis, oligomerization, and processing. Virology 209, 592-603.
34. Plonsky, I., and Zimmerberg, J. (1996). The initial fusion pore induced by baculovirus GP64 is large and forms quickly. J. Cell biol. 135, 1831-1839.
35. Ratinov, V., Plonsky, I., and Zimmerberg, J. (1998). Fusion pore conductance: Experimental approaches and theoretical algorithms. Biophys. J. 74, 2374-2387.
36. Southern, P. J., and Berg, P. (1982). Transformation of mammalian cells to antibiotic resistance with a bacterial gene under control of the SV40 early region promoter. J. Mol. Appl. Genet. 1, 327-341.
37. Spruce, A. E., Iwata, A., and Almers, W. (1991). The first millisecond of the pore formed by a fusogenic viral envelope protein during membrane fusion. Proc. Natl. Acad. Sci. USA 88, 3623-3627.
38. Spruce, A. E., Iwata, A., White, J. M., and Almers, W. (1989). Patch clamp studies of single cell-fusion events mediated by a viral protein. Nature 342, 555-558.
39. Tse, F. W., Iwata, A., and Almers, W. (1993). Membrane flux through the pore formed by a fusogenic viral envelope protein during cell fusion. J. Cell Biol. 121, 543-552.
40. Wang, P., Hammer, D. A., and Granados, R. R. (1997). Binding and fusion of Autographa californica nucleopolyhedrovirus to cultured insect cells. J. Gen. Virol. 78, 3081-3089.
41. Zimmerberg, J., Blumenthal, R., Sarkar, D. P., Curran, M., and Morris, S. J. (1994). Restricted movement of lipid and aqueous dyes through pores formed by influenza hemagglutinin during cell fusion. J. Cell Biol. 127, 1885-1894.
42. Zimmerberg, J., Curran, M., and Cohen, F. S. (1991). A lipid/protein complex hypothesis for exocytotic fusion pore formation. Ann. N.Y. Acad. Sci. 635, 307-317.
43. Zimmerberg, J., Curran, M., Cohen, F. S., and Brodwick, M. (1987). Simultaneous electrical and optical measurement show that membrane fusion precedes secretory granule swelling during exocytosis of beige mouse mast cell. Proc. Natl. Acad. Sci. USA 84, 1585-1589.