Related Experiment Video
Updated: Aug 29, 2025

Investigating the Spreading and Toxicity of Prion-like Proteins Using the Metazoan Model Organism C. elegans
Published on: January 8, 2015
Cryo-EM structure of disease-related prion fibrils provides insights into seeding barriers
Qiuye Li1, Christopher P Jaroniec2, Witold K Surewicz3
1Department of Physiology and Biophysics, Case Western Reserve University, Cleveland, OH, USA.
Abstract:
One of the least understood aspects of prion diseases is the structure of infectious prion protein aggregates. Here we report a high-resolution cryo-EM structure of amyloid fibrils formed by human prion protein with the Y145Stop mutation that is associated with a familial prion disease. This structural insight allows us not only to explain previous biochemical findings, but also provides direct support for the conformational adaptability model of prion transmissibility barriers.
Related Concept Videos
Amyloid Fibrils
Amyloid deposits were observed as early as 1639 in the liver and the spleen. In 1854, Rudolph Virchow performed iodine staining,...
Cryo-electron Microscopy
Subviral Agents

