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Updated: Aug 12, 2026

Protein Misfolding Cyclic Amplification of Prions
Published on: November 7, 2012
Mouse models for studying the formation and propagation of prions
Joel C Watts1, Stanley B Prusiner2
1From the Institute for Neurodegenerative Diseases and the Department of Neurology, University of California, San Francisco, California 94143.
Abstract:
Prions are self-propagating protein conformers that cause a variety of neurodegenerative disorders in humans and animals. Mouse models have played key roles in deciphering the biology of prions and in assessing candidate therapeutics. The development of transgenic mice that form prions spontaneously in the brain has advanced our understanding of sporadic and genetic prion diseases. Furthermore, the realization that many proteins can become prions has necessitated the development of mouse models for assessing the potential transmissibility of common neurodegenerative diseases. As the universe of prion diseases continues to expand, mouse models will remain crucial for interrogating these devastating illnesses.

