Skip to main content
Log in

Evidence for membrane cholesterol as the common binding site for cereolysin, streptolysin O and saponin

  • Published:
Molecular and Cellular Biochemistry Aims and scope Submit manuscript

Summary

Addition of alfalfa saponin to osmotically prepared rabbit erythrocyte membranes resulted in formation of pits or holes as revealed by negative staining followed by electron microscopic examination. The effect on the membranes was quantitatively related to the saponin concentration. Alfalfa saponin also caused disruption of liposomes made of α-lecithin and cholesterol but not of liposomes made of α-lecithin alone. Pretreatment of osmotically prepared erythrocyte membranes with alfalfa saponin prevented ferritin labeling of the membranes by cereolysin-ferritin conjugate, and the degree of inhibition was a function of the concentration of saponin used in pretreatment. Liposomes composed of both lecithin and cholesterol inhibited the hemolytic activity of cereolysin and saponin whereas liposomes containing lecithin only did not. Incubation of cereolysin or streptolysin O with untreated erythrocyte membranes caused complete inhibition of hemolytic activity whereas incubation with erythrocyte membranes pretreated with cereolysin, streptolysin O, filipin or alfalfa saponin did not. Incubation of cereolysin or streptolysin O with erythrocyte membranes pretreated with soybean saponin resulted in complete inhibition of hemolysis. The results provide strong support for the idea that alfalfa saponin, filipin, cereolysin and streptolysin O share a common membrane binding site and the binding site is cholesterol.

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

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. S. P. Halbert, inMicrobial Toxins (T. C. Montie, S. Kadis and S. J. Ajl, ed.), Vol. 3, p. 69–98, Academic Press, N.Y. (1970).

    Google Scholar 

  2. A. W. Bernheimer and P. Grushoff, J. Gen. Microbiol. 46, 143–150 (1967).

    PubMed  Google Scholar 

  3. I. R. Pendleton, K. S. Kim and A. W. Bernheimer, J. Bacteriol. 110, 722–730 (1972).

    PubMed  Google Scholar 

  4. M. M. Weber and S. C. Kinsky, J. Bacteriol. 89, 306–312 (1965).

    PubMed  Google Scholar 

  5. B. Gestetner, S. Shany and Y. Assa, Experientia 27, No. 1, 40–41 (1971).

    PubMed  Google Scholar 

  6. S. Shany, P. S. Grushoff and A. W. Bernheimer, Infect. Immunity 7, 731–734 (1973).

    Google Scholar 

  7. V. A. Fischetti, E. C. Gotschlich and A. W. Bernheimer, J. Exptl. Med. 133, 1105–1117 (1971).

    Google Scholar 

  8. J. Sri Ram, S. S. Tawde, G. B. Pierce and A. R. Midgley, J. Cell Biol. 17, 673–675 (1963).

    PubMed  Google Scholar 

  9. S. Shany, Y. Birk, B. Gestetner and A. Bondi, J. Sci. Fd. Agric. 21, 131–135 (1970).

    Google Scholar 

  10. Y. Birk, A. Bondi, B. Gestetner and I. Ishaaya, Nature 197, 1089–1090 (1963).

    Google Scholar 

  11. A. W. Bernheimer and L. L. Schwartz, J. Gen. Microbiol. 30, 455–468 (1963).

    PubMed  Google Scholar 

  12. A. W. Bernheimer and P. Grushoff, J. Bacteriol. 93, 1541–1543 (1967).

    PubMed  Google Scholar 

  13. J. E. Alouf and M. Raynaud, Ann. Inst. Pasteur 115, 97–121 (1968).

    Google Scholar 

  14. T. D. Oberly and J. L. Duncan, Infect. Immunity 4, 683–687 (1971).

    Google Scholar 

  15. A. W. Bernheimer, Science 159, 847–851 (1968).

    PubMed  Google Scholar 

  16. E. D. Walter, G. B. Van Atta, C. R. Thompson and W. D. Maclay, J. Am. Chem. Soc. 76, 2271–2273 (1954).

    Google Scholar 

  17. B. Gestetner, Y. Assa, Y. Henis, Y. Tencer, M. Rotman, Y. Birk and A. Bondi, Biochim. Biophys. Acta 270, 181–187 (1972).

    PubMed  Google Scholar 

  18. R. R. Dourmaskin, R. M. Dougherty and R. J. Harris, Nature 194, 1116–1119 (1962).

    PubMed  Google Scholar 

  19. J. A. Lucy and A. M. Glauert, J. Mol. Biol. 8, 727–748 (1964).

    Google Scholar 

  20. Y. Assa, S. Shany, B. Gestetner, Y. Tencer, Y. Birk and A. Bondi, Biochim. Biophys. Acta 307, 83–91 (1973).

    PubMed  Google Scholar 

  21. M. K. Johnson, Infect. Immunity 6, 755–760 (1972).

    Google Scholar 

  22. F. Schroeder, J. F. Holland and L. I. Bieber, J. Antibiotic 24, 846–849 (1971).

    Google Scholar 

  23. Y. Birk, inToxic constituents of plant foodstuffs (I. E. Liener, ed.), p. 169–210, Academic Press, New York (1969).

    Google Scholar 

  24. W. C. Davis, Science 175, 1006–1008 (1972).

    PubMed  Google Scholar 

  25. A. W. Bernheimer, K. S. Kim, C. C. Remsen, J. Antanavage and S. W. Watson, Infect. Immunity 6, 636–642 (1972).

    Google Scholar 

  26. A. W. Bernheimer, inMicrobial Toxins (T. C. Montie, S. Kadis and S. J. Ajl, ed.), Vol. 1, p. 183–212, Academic Press, New York (1970).

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Shany, S., Bernheimer, A.W., Grushoff, P.S. et al. Evidence for membrane cholesterol as the common binding site for cereolysin, streptolysin O and saponin. Mol Cell Biochem 3, 179–186 (1974). https://doi.org/10.1007/BF01686643

Download citation

  • Received:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01686643

Keywords

Navigation