Skip to main content

Purification by Two-Phase Partitioning of an Hepatitis Core Protein-Pertussis Epitope Fusion,Expressed in Yeast

  • Chapter

Abstract

It is known that a six amino acid epitope of p69, a membrane protein of Bordetella pertussis, is involved in protection against whooping cough. Chimeric particles were obtained when a thirty amino acid peptide containing the epitope was genetically fused to the hepatitis B virus core antigen and expressed in yeast. The particles were purified by extracting the centrifuged yeast homogenate in a two-phase system composed of PEG 1450 and K phosphate. In this first step, a ten times enrichment was obtained with a total recovery of 45% of the particles. Ninety percent of these were found in the PEG phase. PEG was removed by diafiltration through a YM 100 Amicon membrane with simultaneous concentration of the particles. Gel filtration through a Trisacryl GF 2000 column achieved a good purification and an homogenous preparation as shown by electron microscopy. Immunoaffinity as an alternative to two-phase partitioning will be discussed as well as the advantages of the described protocol for large scale purification of particles.

This is a preview of subscription content, log in via an institution.

Buying options

Chapter
USD   29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD   39.99
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD   54.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Learn about institutional subscriptions

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  1. Lerner, R.A., Green, N., Alexander, H., (1981) Proc. Natl. Acad. Sci. USA 78. 3403–3407.

    Google Scholar 

  2. Emini, E.A., Jameson, B.A., and Wimmer, E., (1983) Nature 304, 699–703.

    Article  PubMed  CAS  Google Scholar 

  3. Zavala, F., Tam, J.P., Hollingdale, M.R., Cochrane, A.H. Quakyi, I., Nussenzweig, R.S., and Nussenzweig, V., (1985) Science 228, 1436–1440.

    Article  PubMed  CAS  Google Scholar 

  4. Clarke, B.E., Newston, S.E., Carroll, A.R., Francis, M.J., Appleyard, G., Syred, A.D., Highfield, P.E., Rowlands, D.J. and Brown, F., (1987) Nature 330, 381–384.

    Article  PubMed  CAS  Google Scholar 

  5. Milich, D.R., and McLachlan, A., (1986) Science 234 1398–1401.

    Article  PubMed  CAS  Google Scholar 

  6. (6) Mortimer, E.A., (1988) Vaccines 74-79 Ed. Plotkin, S.A. and Mortimer, E.A., Pub. by W.B. Saunders & Co.

    Google Scholar 

  7. Novotny, P., Kobisch. M., Cownley, K. Chubb, A.P., and Montaraz, J.A., (1985) Infect, and Imnun. 50, 190–198.

    CAS  Google Scholar 

  8. Montaraz, J.A., Novotny, P., and Ivanyi, J., (1985) Infect, and Immun. 467, 744–751.

    Google Scholar 

  9. Charles, I.G., Dougan, G., Pickard, D., Chatfield, S. Smith, M. Novotny, P., Morrisey, P. and Fairweather N.F., (1989) Proc. Natl. Acad. Sci. 86 3554–3558.

    Article  PubMed  CAS  Google Scholar 

  10. Albertsson, P.A., (1971) Partition of Cell Particles and Macromolecules 2nd Ed. Wiley Interscience.

    Google Scholar 

  11. Laemmli. U.K., (1970) Nature 227, 680–685.

    Article  PubMed  CAS  Google Scholar 

  12. Nilsson, K., Norrlow, O., and Mosbach, K., (1981) Acta. Chem. Scand. B. 35 19–27.

    Article  Google Scholar 

  13. Nilsson, K., and Mosbach, K., (1981) Biochem. Biophys. Res. Commun. 102 449–457.

    Article  PubMed  CAS  Google Scholar 

  14. Beesley, J.E., Day, S.E.J., Betts, M.P. and Thorley, C.M. (1984) J. Gen. Microbiol. 130 1481–1487.

    PubMed  CAS  Google Scholar 

  15. Serwer, P., (1986). Methods in Enzymology 130, 116-132. Ed. C.H.W. Hirs & S.N.T. Timasheff. Acad. Press Inc.

    Google Scholar 

  16. Pasek, M., Goto, T, Gilbert, W., Zuik, B., Schaller, H., MacKay, P., Leadbetter, G., and Murray, K. (1979) Nature 282, 575–579.

    Article  PubMed  CAS  Google Scholar 

  17. Argos, P., and Fuller, S.D. (1988) Embo J. 7, 819–824.

    PubMed  CAS  Google Scholar 

  18. Wasserman, G.F., Inacker, R., Silverman, C.C., and Rosenberg, M., (1987) Protein Purification: Micro to Macro p.337-354. Ed.Alan R. Liss, Inc.

    Google Scholar 

  19. Stahl, S.J. and Murray, K., (1989) Proc. Natl. Acad. Sci. USA 86, 6283–6287.

    Article  PubMed  CAS  Google Scholar 

  20. Kniskern, P.J., Hagopian, A., Montgomery, D.L., Burke, P., Dunn, N.R Hofman, K.J., Miller, W.J., and Ellis, R.W., (1986) Gene 46 135–141.

    Article  PubMed  CAS  Google Scholar 

  21. Miyanohara, A., Imamura, T., Araki, M. Sugawara, K., Ohtomo, N., and Matsubara, K., (1986) J. Virol. 59 176–180.

    PubMed  CAS  Google Scholar 

  22. Milich, D.R., McLachlan, A., Stahl, S., Wingfield, P., Thornton, G.B Hughes, J.L., and Jones, J.E. (1988). J,. Immunol. 141, 3617–3624.

    PubMed  CAS  Google Scholar 

  23. Okada, K., Kamiyama, I., Inomata, M., Imai, M., Miyakawa, Y., and Mayumi, M., (1976) N. Engl. J. Med. 294, 746–749.

    Article  PubMed  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 1990 SCI

About this chapter

Cite this chapter

Riveros-Moreno, V., Beesley, J.E. (1990). Purification by Two-Phase Partitioning of an Hepatitis Core Protein-Pertussis Epitope Fusion,Expressed in Yeast. In: Pyle, D.L. (eds) Separations for Biotechnology 2. Springer, Dordrecht. https://doi.org/10.1007/978-94-009-0783-6_25

Download citation

  • DOI: https://doi.org/10.1007/978-94-009-0783-6_25

  • Publisher Name: Springer, Dordrecht

  • Print ISBN: 978-94-010-6839-0

  • Online ISBN: 978-94-009-0783-6

  • eBook Packages: Springer Book Archive

Publish with us

Policies and ethics