Skip to main content
European Commission logo print header

Alzheimer's disease and Zinc: the missing link ?

Descrizione del progetto

Rame: potenziale bersaglio terapeutico per la malattia di Alzheimer?

La malattia di Alzheimer è un disturbo neurodegenerativo associato all’accumulo anomalo del peptide beta amiloide. Le prove emergenti indicano che gli ioni metallici, soprattutto rame e zinco, si legano al peptide beta amiloide. Il progetto aLzINK, finanziato dal Consiglio europeo della ricerca, lavora sull’ipotesi che questi ioni metallici influenzino in qualche modo la fisiopatologia della malattia di Alzheimer. L’obiettivo principale è studiare i meccanismi sottostanti, la natura dei legami e il possibile impatto tossico di questi ioni metallici. I ricercatori svilupperanno inoltre nuovi farmaci candidati in grado di colpire selettivamente il rame (rispetto allo zinco) legato all’amiloide beta, con l’obiettivo di interromperne gli effetti dannosi.

Obiettivo

Alzheimer's disease (AD) is one of the most serious diseases mankind is now facing as its social and economical impacts are increasing fastly. AD is very complex and the amyloid-β (Aβ) peptide as well as metallic ions (mainly copper and zinc) have been linked to its aetiology. While the deleterious impact of Cu is widely acknowledged, intervention of Zn is certain but still needs to be figured out.

The main objective of the present proposal, which is strongly anchored in the bio-inorganic chemistry field at interface with spectroscopy and biochemistry, is to design, synthesize and study new drug candidates (ligands L) capable of (i) targeting Cu(II) bound to Aβ within the synaptic cleft, where Zn is co-localized and ultimately to develop Zn-driven Cu(II) removal from Aβ and (ii) disrupting the aberrant Cu(II)-Aβ interactions involved in ROS production and Aβ aggregation, two deleterious events in AD. The drug candidates will thus have high Cu(II) over Zn selectively to preserve the crucial physiological role of Zn in the neurotransmission process. Zn is always underestimated (if not completely neglected) in current therapeutic approaches targeting Cu(II) despite the known interference of Zn with Cu(II) binding.

To reach this objective, it is absolutely necessary to first understand the metal ions trafficking issues in presence of Aβ alone at a molecular level (i.e. without the drug candidates).This includes: (i) determination of Zn binding site to Aβ, impact on Aβ aggregation and cell toxicity, (ii) determination of the mutual influence of Zn and Cu to their coordination to Aβ, impact on Aβ aggregation, ROS production and cell toxicity.

Methods used will span from organic synthesis to studies of neuronal model cells, with a major contribution of a wide panel of spectroscopic techniques including NMR, EPR, mass spectrometry, fluorescence, UV-Vis, circular-dichroism, X-ray absorption spectroscopy...

Meccanismo di finanziamento

ERC-STG - Starting Grant

Istituzione ospitante

CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE CNRS
Contribution nette de l'UE
€ 1 372 760,00
Indirizzo
RUE MICHEL ANGE 3
75794 Paris
Francia

Mostra sulla mappa

Regione
Ile-de-France Ile-de-France Paris
Tipo di attività
Research Organisations
Collegamenti
Costo totale
€ 1 499 947,50

Beneficiari (3)