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. 1996 Nov;70(11):7517–7526. doi: 10.1128/jvi.70.11.7517-7526.1996

DNA encapsidation by viruslike particles assembled in insect cells from the major capsid protein VP1 of B-lymphotropic papovavirus.

M Pawlita 1, M Müller 1, M Oppenländer 1, H Zentgraf 1, M Herrmann 1
PMCID: PMC190819  PMID: 8892870

Abstract

Capsids of polyomaviruses--small, nonenveloped DNA viruses--consist of the major structural protein VP1 and the minor structural proteins VP2 and VP3. The contributions of the individual capsid proteins to functions of the viral particle, such as DNA encapsidation, cell receptor attachment, entry, and uncoating, are still not clear. Here we show that viruslike particles assembled in nuclei of insect cells from VP1 of the monkey B-lymphotropic papovavirus (LPV) are sufficient to unspecifically encapsidate DNA. LPV VP1 expressed in large amounts in insect cells by a baculovirus vector assembled spontaneously in the nuclei to form viruslike particles. After metrizamide equilibrium density gradient purification and nuclease digestion, a fraction of these particles was shown to contain VP1-associated linear, double-stranded DNA with a predominant size of 4.5 kb. The fraction of DNA-containing VP1 particles increased with time and dose of baculovirus vector infection. The DNA-containing particles, further purified by sucrose gradient centrifugation, appeared as "full" particles in negative-staining electron microscopy. As shown by DNA hybridization, the encapsidated DNA consisted of insect cell and baculoviral sequences with no apparent strong homology to LPV sequences. Three non-LPV VP1-derived host proteins with apparent molecular masses of approximately 14, 15, and 16 kDa copurified with the DNA-containing particles and may represent insect cell histones encapsidated together with the DNA. A similar species of host DNA was also found in purified LPV wild-type virions. These data suggest that LPV VP1 alone can be sufficient to encapsidate linear DNA in a sequence-independent manner.

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Selected References

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  1. Barouch D. H., Harrison S. C. Interactions among the major and minor coat proteins of polyomavirus. J Virol. 1994 Jun;68(6):3982–3989. doi: 10.1128/jvi.68.6.3982-3989.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Barr S. M., Keck K., Aposhian H. V. Cell-free assembly of a polyoma-like particle from empty capsids and DNA. Virology. 1979 Jul 30;96(2):656–659. doi: 10.1016/0042-6822(79)90124-7. [DOI] [PubMed] [Google Scholar]
  3. Brade L., Vogl W., Gissman L., zur Hausen H. Propagation of B-lymphotropic papovavirus (LPV) in human B-lymphoma cells and characterization of its DNA. Virology. 1981 Oct 15;114(1):228–235. doi: 10.1016/0042-6822(81)90268-3. [DOI] [PubMed] [Google Scholar]
  4. Chang D., Cai X., Consigli R. A. Characterization of the DNA binding properties of polyomavirus capsid protein. J Virol. 1993 Oct;67(10):6327–6331. doi: 10.1128/jvi.67.10.6327-6331.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Clem R. J., Fechheimer M., Miller L. K. Prevention of apoptosis by a baculovirus gene during infection of insect cells. Science. 1991 Nov 29;254(5036):1388–1390. doi: 10.1126/science.1962198. [DOI] [PubMed] [Google Scholar]
  6. Clever J., Dean D. A., Kasamatsu H. Identification of a DNA binding domain in simian virus 40 capsid proteins Vp2 and Vp3. J Biol Chem. 1993 Oct 5;268(28):20877–20883. [PubMed] [Google Scholar]
  7. Forstová J., Krauzewicz N., Sandig V., Elliott J., Palková Z., Strauss M., Griffin B. E. Polyoma virus pseudocapsids as efficient carriers of heterologous DNA into mammalian cells. Hum Gene Ther. 1995 Mar;6(3):297–306. doi: 10.1089/hum.1995.6.3-297. [DOI] [PubMed] [Google Scholar]
  8. Forstová J., Krauzewicz N., Wallace S., Street A. J., Dilworth S. M., Beard S., Griffin B. E. Cooperation of structural proteins during late events in the life cycle of polyomavirus. J Virol. 1993 Mar;67(3):1405–1413. doi: 10.1128/jvi.67.3.1405-1413.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Garber E. A., Seidman M. M., Levine A. J. Intracellular SV40 nucleoprotein complexes: synthesis to encapsidation. Virology. 1980 Dec;107(2):389–401. doi: 10.1016/0042-6822(80)90306-2. [DOI] [PubMed] [Google Scholar]
  10. Griffith J. P., Griffith D. L., Rayment I., Murakami W. T., Caspar D. L. Inside polyomavirus at 25-A resolution. Nature. 1992 Feb 13;355(6361):652–654. doi: 10.1038/355652a0. [DOI] [PubMed] [Google Scholar]
  11. Gruss P., Sauer G. Infectious linear DNA sequences replicating in simian virus 40-infected cells. J Virol. 1977 Feb;21(2):565–578. doi: 10.1128/jvi.21.2.565-578.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Haun G., Keppler O. T., Bock C. T., Herrmann M., Zentgraf H., Pawlita M. The cell surface receptor is a major determinant restricting the host range of the B-lymphotropic papovavirus. J Virol. 1993 Dec;67(12):7482–7492. doi: 10.1128/jvi.67.12.7482-7492.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Herrmann M., Oppenländer M., Pawlita M. Fast and high-affinity binding of B-lymphotropic papovavirus to human B-lymphoma cell lines. J Virol. 1995 Nov;69(11):6797–6804. doi: 10.1128/jvi.69.11.6797-6804.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Keppler O. T., Herrmann M., Oppenländer M., Meschede W., Pawlita M. Regulation of susceptibility and cell surface receptor for the B-lymphotropic papovavirus by N glycosylation. J Virol. 1994 Nov;68(11):6933–6939. doi: 10.1128/jvi.68.11.6933-6939.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Koch M. A., Eggers H. J., Anderer F. A., Schlumberger H. D., Frank H. Structure of simian virus 40. I. Purification and physical characterization of the virus particle. Virology. 1967 Jul;32(3):503–510. doi: 10.1016/0042-6822(67)90302-9. [DOI] [PubMed] [Google Scholar]
  16. Liddington R. C., Yan Y., Moulai J., Sahli R., Benjamin T. L., Harrison S. C. Structure of simian virus 40 at 3.8-A resolution. Nature. 1991 Nov 28;354(6351):278–284. doi: 10.1038/354278a0. [DOI] [PubMed] [Google Scholar]
  17. Mattern C. F., Takemoto K. K., DeLeva A. M. Electron microscopic observations on multiple polyoma virus-related particles. Virology. 1967 Jul;32(3):378–392. doi: 10.1016/0042-6822(67)90288-7. [DOI] [PubMed] [Google Scholar]
  18. Menezes J., Leibold W., Klein G., Clements G. Establishment and characterization of an Epstein-Barr virus (EBC)-negative lymphoblastoid B cell line (BJA-B) from an exceptional, EBV-genome-negative African Burkitt's lymphoma. Biomedicine. 1975 Jul;22(4):276–284. [PubMed] [Google Scholar]
  19. Michel M. R., Hirt B., Weil R. Mouse cellular DNA enclosed in polyoma viral capsids (pseudovirions). Proc Natl Acad Sci U S A. 1967 Oct;58(4):1381–1388. doi: 10.1073/pnas.58.4.1381. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Montross L., Watkins S., Moreland R. B., Mamon H., Caspar D. L., Garcea R. L. Nuclear assembly of polyomavirus capsids in insect cells expressing the major capsid protein VP1. J Virol. 1991 Sep;65(9):4991–4998. doi: 10.1128/jvi.65.9.4991-4998.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Moreland R. B., Montross L., Garcea R. L. Characterization of the DNA-binding properties of the polyomavirus capsid protein VP1. J Virol. 1991 Mar;65(3):1168–1176. doi: 10.1128/jvi.65.3.1168-1176.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Mühlbach P., Pawlita M. A stable flank of unstable lymphotropic papovavirus integration sites is associated with a cellular S1 nuclease-sensitive sequence. Virology. 1992 Jan;186(1):65–73. doi: 10.1016/0042-6822(92)90061-s. [DOI] [PubMed] [Google Scholar]
  23. Oppenheim A., Sandalon Z., Peleg A., Shaul O., Nicolis S., Ottolenghi S. A cis-acting DNA signal for encapsidation of simian virus 40. J Virol. 1992 Sep;66(9):5320–5328. doi: 10.1128/jvi.66.9.5320-5328.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Pawlita M., Clad A., zur Hausen H. Complete DNA sequence of lymphotropic papovavirus: prototype of a new species of the polyomavirus genus. Virology. 1985 May;143(1):196–211. doi: 10.1016/0042-6822(85)90108-4. [DOI] [PubMed] [Google Scholar]
  25. Qasba P. K., Aposhian H. V. DNA and gene therapy: transfer of mouse DNA to human and mouse embryonic cells by polyoma pseudovirions. Proc Natl Acad Sci U S A. 1971 Oct;68(10):2345–2349. doi: 10.1073/pnas.68.10.2345. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Rayment I., Baker T. S., Caspar D. L., Murakami W. T. Polyoma virus capsid structure at 22.5 A resolution. Nature. 1982 Jan 14;295(5845):110–115. doi: 10.1038/295110a0. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Rickwood D., Birnie G. D. Metrizamide, a new density-gradient medium. FEBS Lett. 1975 Feb 1;50(2):102–110. doi: 10.1016/0014-5793(75)80467-4. [DOI] [PubMed] [Google Scholar]
  28. Salunke D. M., Caspar D. L., Garcea R. L. Polymorphism in the assembly of polyomavirus capsid protein VP1. Biophys J. 1989 Nov;56(5):887–900. doi: 10.1016/S0006-3495(89)82735-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Salunke D. M., Caspar D. L., Garcea R. L. Self-assembly of purified polyomavirus capsid protein VP1. Cell. 1986 Sep 12;46(6):895–904. doi: 10.1016/0092-8674(86)90071-1. [DOI] [PubMed] [Google Scholar]
  30. Slilaty S. N., Berns K. I., Aposhian H. V. Polyoma-like particle: characterization of the DNA encapsidated in vitro by polyoma empty capsids. J Biol Chem. 1982 Jun 10;257(11):6571–6575. [PubMed] [Google Scholar]
  31. Soussi T. DNA-binding properties of the major structural protein of simian virus 40. J Virol. 1986 Sep;59(3):740–742. doi: 10.1128/jvi.59.3.740-742.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Tweeten K. A., Bulla L. A., Consigli R. A. Characterization of an extremely basic protein derived from granulosis virus nucleocapsids. J Virol. 1980 Feb;33(2):866–876. doi: 10.1128/jvi.33.2.866-876.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Wilson M. E., Miller L. K. Changes in the nucleoprotein complexes of a baculovirus DNA during infection. Virology. 1986 Jun;151(2):315–328. doi: 10.1016/0042-6822(86)90052-8. [DOI] [PubMed] [Google Scholar]
  34. Wilson M. E., Price K. H. Association of Autographa californica nuclear polyhedrosis virus (AcMNPV) with the nuclear matrix. Virology. 1988 Nov;167(1):233–241. doi: 10.1016/0042-6822(88)90073-6. [DOI] [PubMed] [Google Scholar]
  35. Winocour E. Further studies on the incorporation of cell DNA into polyoma-related particles. Virology. 1968 Apr;34(4):571–582. doi: 10.1016/0042-6822(68)90078-0. [DOI] [PubMed] [Google Scholar]
  36. zur Hausen H., Gissmann L. Lymphotropic papovaviruses isolated from African green monkey and human cells. Med Microbiol Immunol. 1979 Aug;167(3):137–153. doi: 10.1007/BF02121180. [DOI] [PubMed] [Google Scholar]

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