Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

  • Letter
  • Published:

Isolation and quantification of soluble Alzheimer's β-peptide from biological fluids

Abstract

CEREBRAL deposition of the β-amyloid peptide (Aβ) is an invariant feature of Alzheimer's disease. Since the original isola-tion and characterization of αβ (ref. 1) and the subsequent cloning of its precursor protein2–5, no direct evidence for the actual production of discrete Aβ has been reported6–11. Here we investigate whether Aβ is present in human biological fluids using antibodies specific for an epitope within Aβ that spans the site of normal constitutive cleavage12,13. These antibodies were used to construct a sandwich type enzyme-linked immunosorbent assay that detects Aβ in cerebrospinal fluid, plasma and conditioned medium of human mixed-brain cells grown in vitro (see also ref. 14). By affinity chromatography, we have purified and sequenced Aβ and a novel Aβ fragment from human cerebrospinal fluid and conditioned medium of human mixed-brain cell cultures. These findings demonstrate that Aβ is produced and released both in vivo and in vitro. These observations offer new opportunities for developing diagnostic tests for Alzheimer's disease and therapeutic strategies aimed at reducing the cerebral deposition of Aβ.

This is a preview of subscription content, access via your institution

Access options

Buy this article

Prices may be subject to local taxes which are calculated during checkout

Similar content being viewed by others

References

  1. Glenner, G. G. & Wong, C. W. Biochem. biophys. Res. Commun. 120, 885–890 (1984).

    Article  CAS  Google Scholar 

  2. Kang, J. et al. Nature 325, 733–736 (1987).

    Article  CAS  ADS  Google Scholar 

  3. Ponte, P. et al. Nature 331, 525–527 (1988).

    Article  CAS  ADS  Google Scholar 

  4. Tanzi, R. E. et al. Nature 331, 528–530 (1988).

    Article  CAS  ADS  Google Scholar 

  5. Kitaguchi, N., Takahashi, Y., Tokushima, Y., Shiojiri, S. & Ito, H. Nature 331, 530–532 (1988).

    Article  CAS  ADS  Google Scholar 

  6. Joachim, C. L., Mori, H. & Selkoe, D. J. Nature 341, 226–230 (1989).

    Article  CAS  ADS  Google Scholar 

  7. Estus, S. et al. Science 255, 726–728 (1992).

    Article  CAS  ADS  Google Scholar 

  8. Golde, T. et al. Science 255, 728–730 (1992).

    Article  CAS  ADS  Google Scholar 

  9. Tamaoka, A. et al. Proc. natn. Acad. Sci. U.S.A. 89, 1345–1347 (1992).

    Article  CAS  ADS  Google Scholar 

  10. Nordstedt, C. et al. Proc. natn. Acad. Sci. U.S.A. 88, 8910–8914 (1991).

    Article  CAS  ADS  Google Scholar 

  11. Buxbaum, J. D. et al. Proc. natn. Acad. Sci. U.S.A. 87, 6003–6006 (1990).

    Article  CAS  ADS  Google Scholar 

  12. Esch, F. S. et al. Science 248, 1122–1124 (1990).

    Article  CAS  ADS  Google Scholar 

  13. Anderson, J. P. et al. Neurosci. Lett. 128, 126–128 (1991).

    Article  CAS  Google Scholar 

  14. Haass, C. et al. Nature 359, 322–325 (1992).

    Article  CAS  ADS  Google Scholar 

  15. Hyman, B. T. et al. J. Neuropath. exp. Neurol. 51, 76–83 (1992).

    Article  CAS  Google Scholar 

  16. Joachin, C. L. et al. Brain Res. 474, 100–111 (1988).

    Article  Google Scholar 

  17. Mori, H. et al. J. biol. Chem. 267, 17082–17086 (1992).

    CAS  PubMed  Google Scholar 

  18. Prelli, F. et al. J. Neurochem. 51, 648–651 (1988).

    Article  CAS  Google Scholar 

  19. Zagorski, M. G. & Barrow, C. J. Biochemistry 31, 5621–5631 (1992).

    Article  CAS  Google Scholar 

  20. Hilbich, C. et al. J. molec. Biol. 218, 149–163 (1991).

    Article  CAS  Google Scholar 

  21. Goate, A. et al. Nature 349, 704–706 (1991).

    Article  CAS  ADS  Google Scholar 

  22. Chartier-Harlin, M. C. et al. Nature 353, 844–846 (1991).

    Article  CAS  ADS  Google Scholar 

  23. Levy, E. et al. Science 248, 1124–1126 (1990).

    Article  CAS  ADS  Google Scholar 

  24. Murrell, J., Farlow, M., Ghetti, B. & Benson, M. D. Science 254, 97–99 (1991).

    Article  CAS  ADS  Google Scholar 

  25. Köhler, G. & Milstein, C. Nature 256, 495–497 (1975).

    Article  ADS  Google Scholar 

  26. Oi, V. T. et al. Methods in Cellular Immunology Ch. 17 (Freeman, San Francisco, 1990).

    Google Scholar 

  27. Wang, R. W. et al. J. Immun. Meth. 18, 157–164 (1984).

    Article  Google Scholar 

  28. Johnstone, E. M. et al. Molec. Brain Res. 10, 299–305 (1991).

    Article  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Seubert, P., Vigo-Pelfrey, C., Esch, F. et al. Isolation and quantification of soluble Alzheimer's β-peptide from biological fluids. Nature 359, 325–327 (1992). https://doi.org/10.1038/359325a0

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1038/359325a0

This article is cited by

Comments

By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.

Search

Quick links

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing