Aberrant metal binding by prion protein in human prion disease

Academic Article


  • Human prion diseases are characterized by the conversion of the normal prion protein (PrPc) into a pathogenic isomer (PrpSc). Distinct PrPSc conformers are associated with different subtypes of prion diseases. PrPc binds copper and has antioxidation activity. Changes in metal-ion occupancy can lead to significant decline of the antioxidation activity and changes in conformation of the protein. We studied the trace element status of brains from patients with sporadic Creutzfeldt-Jakob disease (sCJD). We found a decrease of up to 50% of copper and an increase in manganese of approximately 10-fold in the brain tissues from sCJD subjects. We have also studied the metal occupancy of PrP in sCJD patients. We observed striking elevation of manganese and, to a lesser extent, of zinc accompanied by significant reduction of copper bound to purified PrP in all sCJD variants, determined by the PrP genotype and PrPsc type, combined. Both zinc and manganese were undetectable in PrPc preparations from controls. Copper and manganese changes were pronounced in sCJD subjects homozygous for methionine at codon 129 and carrying PrPSc type-1. Anti-oxidation activity of purified PrP was dramatically reduced by up to 85% in the sCJD variants, and correlated with increased in oxidative stress markers in sCJD brains. These results suggest that altered metal-ion occupancy of PrP plays a pivotal role in the pathogenesis of prion diseases. Since the metal changes differed in each sCJD variants, they may contribute to the diversity of PrPSc and disease phenotype in sCJD. Finally, this study also presented two potential approaches in the diagnosis of CJD; the significant increase in brain manganese makes it potentially detectable by MRI, and the binding of manganese by PrP in sCJD might represent a novel diagnostic marker.
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    Author List

  • Wong BS; Chen SG; Colucci M; Xie Z; Pan T; Liu T; Li R; Gambetti P; Sy MS; Brown DR
  • Start Page

  • 1400
  • End Page

  • 1408
  • Volume

  • 78
  • Issue

  • 6