Gaudreault, Roger; Hervé, Vincent; Van De Ven, Theo; Mousseau, Normand et Ramassamy, Charles 
ORCID: https://orcid.org/0000-0002-3252-5878
(2021).
Polyphenol-Peptide Interactions in Mitigation of Alzheimer's Disease: Role of Biosurface-Induced Aggregation
Journal of Alzheimer's Disease
, vol. 81
, nº 1.
pp. 33-55.
DOI: 10.3233/jad-201549.
Résumé
Alzheimer's disease (AD) is the most common age-related neurodegenerative disorder, responsible for nearly two-thirds of all dementia cases. In this review, we report the potential AD treatment strategies focusing on natural polyphenol molecules (green chemistry) and more specifically on the inhibition of polyphenol-induced amyloid aggregation/disaggregation pathways: in bulk and on biosurfaces. We discuss how these pathways can potentially alter the structure at the early stages of AD, hence delaying the aggregation of amyloid-β (Aβ) and tau. We also discuss multidisciplinary approaches, combining experimental and modelling methods, that can better characterize the biochemical and biophysical interactions between proteins and phenolic ligands. In addition to the surface-induced aggregation, which can occur on surfaces where protein can interact with other proteins and polyphenols, we suggest a new concept referred as "confinement stability". Here, on the contrary, the adsorption of Aβ and tau on biosurfaces other than Aβ- and tau-fibrils, e.g., red blood cells, can lead to confinement stability that minimizes the aggregation of Aβ and tau. Overall, these mechanisms may participate directly or indirectly in mitigating neurodegenerative diseases, by preventing protein self-association, slowing down the aggregation processes, and delaying the progression of AD.
| Type de document: | Article |
|---|---|
| Mots-clés libres: | Alzheimer’s Disease; Amyloid; Blood Cells; Computer Simulation; Polyphenols; Tau |
| Centre: | Centre INRS-Institut Armand Frappier |
| Date de dépôt: | 23 juin 2022 02:26 |
| Dernière modification: | 23 juin 2022 02:26 |
| URI: | https://espace.inrs.ca/id/eprint/12335 |
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