Metal ions, dopamine, and oxidative stress in Parkinson's disease

Progetti nazionali
Programma di ricerca
PRIN 2015
Ente finanziatore
Settore ERC
LS5_2 - Molecular and cellular neuroscience
PE5_10 - Coordination chemistry
PE5_12 - Biological chemistry
02/02/2017 - 01/02/2017
Tegoni Matteo

Aree / Gruppi di ricerca

Partecipanti al progetto

Descrizione del progetto

Dopaminergic neurons in the substantia nigra, a small region of the mid brain producing dopamine, undergo extensive and selective loss with the progression of Parkinson's disease (PD), with less substantial death in other brain regions. The surviving dopaminergic cells of PD patients contain cytosolic filamentous inclusions known as Lewy bodies, within which α-synuclein (αSyn) is a major component. Neurofibrillary tangles, containing aggregated tau, are also present. Accumulation of toxic forms of αSyn is considered a critical step in the development of PD, and it is currently accepted that these toxic forms are protofibrillar aggregates of αSyn and post-transactionally modified αSyn. The pattern of post-translational αSyn modifications identified in cytosolic aggregates in experimental models and PD brains include oxidation, nitration, and phosphorylation, but the form of αSyn that is thought to be mostly responsible for neuron toxicity is the oligomeric protein resulting from the interaction with oxidized dopamine. The role of dopamine is intriguing, as this neurotransmitter is also involved in the biosynthesis of neuromelanin (NM), the pigment contained in substantia nigra neurons, which is formed upon extensive oxidative oligomerization of dopamine and conjugation with protein/peptides.

Oxidative stress and redox metal ions are strong determinants of post-translational modifications of αSyn and other neuronal proteins like tau. In this project, we plan to perform a systematic, quantitative and comparative study of the redox reactivity, capacity of generating ROS and RNS, and catalytic oxidative activity of thoroughly characterized iron and copper complexes with αSyn and tau. We believe this is the necessary step to enable a reliable assessment of the toxicity of metal ions bound to neuronal proteins and peptides in a given environment. The toxicity associated with ROS production by metal-αSyn and metal-tau peptides will be evaluated in cellular models.

The project develops along several, inter-related research lines:

1) Binding characteristics, ROS production, dopamine oxidation, and protein modification by Cu and Fe complexes with N-acetylated αSyn (Ac-αSyn) in solution and membrane environment.

2) Reactions of Cu- and Fe-Ac-αSyn complexes with NO donors, production of RNS, and protein nitration.

3) Binding and reactivity behavior of Cu and Fe complexes with oxidized, nitrated, and phosphorylated Ac-αSyn.

4) Interaction of Fe and Cu with tau fragments: binding, redox behavior, ROS and RNS production, reactivity towards biological substrates.

5) Heme toxicity: binding and reactivity behavior with tau and β-amyloid

6) ROS production by Cu and Fe complexes with αSyn and tau in cellular models

7) Protein target modification by ROS/RNS and dopamine in cells

8) Dopamination of proteins and biosynthetic pathway to NM



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