Copper(I/II), α/β‐Synuclein and Amyloid‐β: Menage à Trois?. Issue 16 (25th September 2015)
- Record Type:
- Journal Article
- Title:
- Copper(I/II), α/β‐Synuclein and Amyloid‐β: Menage à Trois?. Issue 16 (25th September 2015)
- Main Title:
- Copper(I/II), α/β‐Synuclein and Amyloid‐β: Menage à Trois?
- Authors:
- De Ricco, Riccardo
Valensin, Daniela
Dell'Acqua, Simone
Casella, Luigi
Hureau, Christelle
Faller, Peter - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>Copper binding to α‐synuclein (aS) and to amyloid‐β (Ab) has been connected to Parkinson's and Alzheimer's disease (AD), respectively, because Cu ions can modulate the peptide aggregation, and these Cu<bold>⋅</bold>peptide complexes can catalyse the production of reactive oxygen species (ROS). In a significant proportion of AD brains, aggregation of aS and Ab has been detected, and it was proposed that Ab and aS interact with each other. Thus, we investigated the potential interactions of Ab and aS through their binding of copper(I) and copper(II). Additionally, β‐synuclein (bS) was investigated, due to its additional methionine residue, a potential Cu<sup>I</sup> ligand. We found that: 1) the peptides containing the Cu‐binding domains Ab1–16, aS1–15 and bS1–15 have similar affinities towards Cu<sup>II</sup> and towards Cu<sup>I</sup>, with Ab1–16 being slightly stronger, 2) in the case of Cu<sup>I</sup>, the additional Met residue in bS1–15 increased the affinity slightly, 3) the exchange of Cu<sup>I/II</sup> between the two peptides is rapid (≤ms), 4) a/bS1–15 and Ab1–16 form a heterodimeric complex with Cu<sup>II</sup>, 5) Cu<sup>I</sup> probably promotes a transient ternary complex, 6) the different Cu<sup>I/II</sup> coordination of Ab1–16, aS1–15 and bS1–15 impacts the capacity to produce ROS and to oxidise catechol, and 7) when Ab1–16, aS1–15 and Cu are present, the ROS production more closely<abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>Copper binding to α‐synuclein (aS) and to amyloid‐β (Ab) has been connected to Parkinson's and Alzheimer's disease (AD), respectively, because Cu ions can modulate the peptide aggregation, and these Cu<bold>⋅</bold>peptide complexes can catalyse the production of reactive oxygen species (ROS). In a significant proportion of AD brains, aggregation of aS and Ab has been detected, and it was proposed that Ab and aS interact with each other. Thus, we investigated the potential interactions of Ab and aS through their binding of copper(I) and copper(II). Additionally, β‐synuclein (bS) was investigated, due to its additional methionine residue, a potential Cu<sup>I</sup> ligand. We found that: 1) the peptides containing the Cu‐binding domains Ab1–16, aS1–15 and bS1–15 have similar affinities towards Cu<sup>II</sup> and towards Cu<sup>I</sup>, with Ab1–16 being slightly stronger, 2) in the case of Cu<sup>I</sup>, the additional Met residue in bS1–15 increased the affinity slightly, 3) the exchange of Cu<sup>I/II</sup> between the two peptides is rapid (≤ms), 4) a/bS1–15 and Ab1–16 form a heterodimeric complex with Cu<sup>II</sup>, 5) Cu<sup>I</sup> probably promotes a transient ternary complex, 6) the different Cu<sup>I/II</sup> coordination of Ab1–16, aS1–15 and bS1–15 impacts the capacity to produce ROS and to oxidise catechol, and 7) when Ab1–16, aS1–15 and Cu are present, the ROS production more closely resembles that by Ab1–16. The work gives insights into the coordination chemistry of these related peptides, and the relevance of coordination differences, the ternary complex and ROS production are discussed.</p> </abstract> … (more)
- Is Part Of:
- Chembiochem. Volume 16:Issue 16(2015)
- Journal:
- Chembiochem
- Issue:
- Volume 16:Issue 16(2015)
- Issue Display:
- Volume 16, Issue 16 (2015)
- Year:
- 2015
- Volume:
- 16
- Issue:
- 16
- Issue Sort Value:
- 2015-0016-0016-0000
- Page Start:
- 2319
- Page End:
- 2328
- Publication Date:
- 2015-09-25
- Subjects:
- Biochemistry -- Periodicals
Molecular biology -- Periodicals
Pharmaceutical chemistry -- Periodicals
572 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7633 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/cbic.201500425 ↗
- Languages:
- English
- ISSNs:
- 1439-4227
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3133.490980
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 4328.xml