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α-synuclein implicated in Parkinson’s disease catalyses the formation of hydrogen peroxide in vitro.

Research output: Contribution to Journal/MagazineJournal articlepeer-review

<mark>Journal publication date</mark>15/05/2001
<mark>Journal</mark>Free Radical Biology and Medicine
Issue number10
Number of pages8
Pages (from-to)1163-1170
Publication StatusPublished
<mark>Original language</mark>English


Some rare inherited forms of Parkinson’s disease (PD) are due to mutations in the gene encoding a 140-amino acid presynaptic protein called -synuclein. In PD, and some other related disorders such as dementia with Lewy bodies, -synuclein accumulates in the brain in the form of fibrillar aggregates, which are found inside the neuronal cytoplasmic inclusions known as Lewy bodies. By means of an electron spin resonance (ESR) spin trapping method, we show here that solutions of full-length -synuclein, and a synthetic peptide fragment of -synuclein corresponding to residues 61–95 (the so-called non-Aβ component or NAC), both liberate hydroxyl radicals upon incubation in vitro followed by the addition of Fe(II). We did not observe this property for the related β- and γ-synucleins, which are not found in Lewy bodies, and are not linked genetically to any neurodegenerative disorder. There is abundant evidence for the involvement of free radicals and oxidative stress in the pathogenesis of nigral damage in PD. Our new data suggest that the fundamental molecular mechanism underlying this pathological process could be the production of hydrogen peroxide by -synuclein.