Abstract
In prion diseases, metal imbalances in brain and/or metal substitutions for copper in prion protein suggest that metal-catalyzed oxidation (MCO) and oxidative stress may affect cellular function and accumulation of protease-resistant prion protein (PrP Sc). We examined the effect of metal-induced oxidative stress by Fenton reaction on prion protein with regard to its degradation, insolubility, and infectivity. Precipitation and insolubility of prion protein were induced by Fenton reaction in scrapie-infected brain homogenate. Results showed an increase in hydroxylation products (thiobarbituric acid reactive substances; TBARS) and a decrease of ferrous ion (Fe 2+) levels after Fenton reaction. Efficiency of metal-induced oxidation was higher for Fe 2+ than Mn 2+. Compared to untreated samples, there was increased susceptibility to proteolytic degradation of PrP Sc after treatment with 3.12–12.5 mM Fe 2+–Mn 2+/H 2O 2. Interestingly, we observed that Fenton reaction could extend incubation periods, indicating a decrease in scrapie infectivity. These results suggest that PrP Sc hydroxylation and degradation may affect PrP conversion and the pathogenesis of prion diseases.
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