Chemistry of mammalian metallothioneins and their interaction with amyloidogenic peptides and proteins12. (8th November 2017)
- Record Type:
- Journal Article
- Title:
- Chemistry of mammalian metallothioneins and their interaction with amyloidogenic peptides and proteins12. (8th November 2017)
- Main Title:
- Chemistry of mammalian metallothioneins and their interaction with amyloidogenic peptides and proteins12
- Authors:
- Atrián-Blasco, Elena
Santoro, Alice
Pountney, Dean L.
Meloni, Gabriele
Hureau, Christelle
Faller, Peter - Abstract:
- Abstract : Tutorial focusing on the chemistry of mammalian metallothioneins, important to understand its biological functions in zinc and copper metabolism, detoxification and oxidative stress. Abstract : Cu and Zn ions are essential in most living beings. Their metabolism is critical for health and mis-metabolism can be lethal. In the last two decades, a large body of evidence has reported the role of copper, zinc and iron, and oxidative stress in several neurodegenerative diseases like Alzheimer's, Parkinson's, prion diseases, etc. To what extent this mis-metabolism is causative or a consequence of these diseases is still a matter of research. In this context metallothioneins (MTs) appear to play a central gate-keeper role in controlling aberrant metal–protein interactions. MTs are small proteins that can bind high amounts of Zn(ii ) and Cu(i ) ions in metal-cluster arrangements via their cysteine thiolates. Moreover, MTs are well known antioxidants. The present tutorial outlines the chemistry underlying the interconnection between copper(i /ii ) and zinc(ii ) coordination to amyloidogenic proteins and MTs, and their redox properties in generation and/or silencing reactive oxygen species (overproduced in oxidative stress) and other reactants. These studies have revealed the coordination chemistry involved in neurodegenerative diseases and the interactions between MTs and amyloidogenic protein metal-complexes (like amyloid-β, α-synuclein and prion-protein). Overall, theAbstract : Tutorial focusing on the chemistry of mammalian metallothioneins, important to understand its biological functions in zinc and copper metabolism, detoxification and oxidative stress. Abstract : Cu and Zn ions are essential in most living beings. Their metabolism is critical for health and mis-metabolism can be lethal. In the last two decades, a large body of evidence has reported the role of copper, zinc and iron, and oxidative stress in several neurodegenerative diseases like Alzheimer's, Parkinson's, prion diseases, etc. To what extent this mis-metabolism is causative or a consequence of these diseases is still a matter of research. In this context metallothioneins (MTs) appear to play a central gate-keeper role in controlling aberrant metal–protein interactions. MTs are small proteins that can bind high amounts of Zn(ii ) and Cu(i ) ions in metal-cluster arrangements via their cysteine thiolates. Moreover, MTs are well known antioxidants. The present tutorial outlines the chemistry underlying the interconnection between copper(i /ii ) and zinc(ii ) coordination to amyloidogenic proteins and MTs, and their redox properties in generation and/or silencing reactive oxygen species (overproduced in oxidative stress) and other reactants. These studies have revealed the coordination chemistry involved in neurodegenerative diseases and the interactions between MTs and amyloidogenic protein metal-complexes (like amyloid-β, α-synuclein and prion-protein). Overall, the protective role of MTs in neurodegenerative processes is emerging, serving as a foundation for exploring MT chemistry as inspiration for therapeutic approaches. … (more)
- Is Part Of:
- Chemical Society reviews. Volume 46:Number 24(2017)
- Journal:
- Chemical Society reviews
- Issue:
- Volume 46:Number 24(2017)
- Issue Display:
- Volume 46, Issue 24 (2017)
- Year:
- 2017
- Volume:
- 46
- Issue:
- 24
- Issue Sort Value:
- 2017-0046-0024-0000
- Page Start:
- 7683
- Page End:
- 7693
- Publication Date:
- 2017-11-08
- Subjects:
- Chemistry -- Periodicals
540 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/cs#!recentarticles&adv ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c7cs00448f ↗
- Languages:
- English
- ISSNs:
- 0306-0012
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3151.550000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 5490.xml