Chemical chaperones interfere with the formation of scrapie prion protein

EMBO J. 1996 Dec 2;15(23):6363-73.


The fundamental event in prion diseases involves a conformational change in one or more of the alpha-helices of the cellular prion protein (PrP(C)) as they are converted into beta-sheets during the formation of the pathogenic isoform (PrP(Sc)). Here, we show that exposure of scrapie-infected mouse neuroblastoma (ScN2a) cells to reagents known to stabilize proteins in their native conformation reduced the rate and extent of PrP(Sc) formation. Such reagents include the cellular osmolytes glycerol and trimethylamine N-oxide (TMAO) and the organic solvent dimethylsulfoxide (DMSO), which we refer to as 'chemical chaperones' because of their influence on protein folding. Although the chemical chaperones did not appear to affect the existing population of PrP(Sc) molecules in ScN2a cells, they did interfere with the formation of PrP(Sc) from newly synthesized PrP(C). We suggest that the chemical chaperones act to stabilize the alpha-helical conformation of PrP(C) and thereby prevent the protein from undergoing a conformational change to produce PrP(Sc). These observations provide further support for the idea that prions arise due to a change in protein conformation and reveal potential strategies for preventing PrP(Sc) formation.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Brain / metabolism*
  • Cell Line
  • Dimethyl Sulfoxide / pharmacology
  • Glycerol / pharmacology
  • Kinetics
  • Methylamines / pharmacology*
  • Mice
  • Molecular Chaperones*
  • Neuroblastoma
  • Phospholipases
  • PrPSc Proteins / biosynthesis*
  • PrPSc Proteins / chemistry*
  • PrPSc Proteins / drug effects
  • Protein Folding*
  • Protein Structure, Secondary
  • Reference Values
  • Scrapie / metabolism*
  • Solubility
  • Tumor Cells, Cultured


  • Methylamines
  • Molecular Chaperones
  • PrPSc Proteins
  • Phospholipases
  • trimethyloxamine
  • Glycerol
  • Dimethyl Sulfoxide