Skip to main content

Advertisement

Log in

Prion: the chameleon protein

  • Visions & Reflections (Minireview)
  • Published:
Cellular and Molecular Life Sciences Aims and scope Submit manuscript

Abstract.

From Creutzfeldt-Jakob disease (CJD) to variant CJD through Gerstmann-Sträussler-Scheinker syndrome, kuru and fatal familial insomnia, the journey leading to current understanding of the basic aspects of human prion diseases has been full of unexpected, but often dramatic and always fascinating twists. Recent progress in modeling prion diseases and characterization of the various prion protein forms reveal that such a wide spectrum of the diseases is associated with the chameleon-like conformational features of prions.

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

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to W. Q. Zou.

Additional information

Received 19 August 2007; received after revision 2 October 2007; accepted 10 October 2007

Rights and permissions

Reprints and permissions

About this article

Cite this article

Zou, W.Q., Gambetti, P. Prion: the chameleon protein. Cell. Mol. Life Sci. 64, 3266–3270 (2007). https://doi.org/10.1007/s00018-007-7380-8

Download citation

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00018-007-7380-8

Keywords.

Navigation