Article
Dominant prion mutants induce curing through pathways that promote chaperone-mediated disaggregation.
Nature structural & molecular biology - 1 Apr 2011
DiSalvo Susanne, Derdowski Aaron, Pezza John A, Serio Tricia R
Abstract excerpt
Protein misfolding underlies many neurodegenerative diseases, including the transmissible spongiform encephalopathies (prion diseases). Although cells typically recognize and process misfolded proteins, prion proteins evade protective measures by forming stable, self-replicating aggregates. However, coexpression of dominant-negative prion mutants can overcome aggregate accumulation and disease progression through...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
