Metal binding to the amyloid-β peptides in the presence of biomembranes: potential mechanisms of cell toxicity.
Amyloid disease
Amyloid-beta peptide
Cytotoxicity
Membrane pore
Phospholipid membrane
Reactive oxygen species
Redox-active metal ion
Journal
Journal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry
ISSN: 1432-1327
Titre abrégé: J Biol Inorg Chem
Pays: Germany
ID NLM: 9616326
Informations de publication
Date de publication:
12 2019
12 2019
Historique:
received:
04
06
2019
accepted:
10
09
2019
pubmed:
29
9
2019
medline:
11
8
2020
entrez:
29
9
2019
Statut:
ppublish
Résumé
The amyloid-β (Aβ) peptides are key molecules in Alzheimer's disease (AD) pathology. They interact with cellular membranes, and can bind metal ions outside the membrane. Certain oligomeric Aβ aggregates are known to induce membrane perturbations and the structure of these oligomers-and their membrane-perturbing effects-can be modulated by metal ion binding. If the bound metal ions are redox active, as e.g., Cu and Fe ions are, they will generate harmful reactive oxygen species (ROS) just outside the membrane surface. Thus, the membrane damage incurred by toxic Aβ oligomers is likely aggravated when redox-active metal ions are present. The combined interactions between Aβ oligomers, metal ions, and biomembranes may be responsible for at least some of the neuronal death in AD patients.
Identifiants
pubmed: 31562546
doi: 10.1007/s00775-019-01723-9
pii: 10.1007/s00775-019-01723-9
doi:
Substances chimiques
Amyloid beta-Peptides
0
Reactive Oxygen Species
0
Copper
789U1901C5
Iron
E1UOL152H7
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Review
Langues
eng
Sous-ensembles de citation
IM