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Alpha-Synuclein Is a Cellular Ferrireductase

α-synuclein (αS) is a cellular protein mostly known for the association of its aggregated forms with a variety of diseases that include Parkinson's disease and Dementia with Lewy Bodies. While the role of αS in disease is well documented there is currently no agreement on the physiological func...

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Detalles Bibliográficos
Autores principales: Davies, Paul, Moualla, Dima, Brown, David R.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3018422/
https://www.ncbi.nlm.nih.gov/pubmed/21249223
http://dx.doi.org/10.1371/journal.pone.0015814
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author Davies, Paul
Moualla, Dima
Brown, David R.
author_facet Davies, Paul
Moualla, Dima
Brown, David R.
author_sort Davies, Paul
collection PubMed
description α-synuclein (αS) is a cellular protein mostly known for the association of its aggregated forms with a variety of diseases that include Parkinson's disease and Dementia with Lewy Bodies. While the role of αS in disease is well documented there is currently no agreement on the physiological function of the normal isoform of the protein. Here we provide strong evidence that αS is a cellular ferrireductase, responsible for reducing iron (III) to bio available iron (II). The recombinant form of the protein has a V(Max) of 2.72 nmols/min/mg and K(m) 23 µM. This activity is also evident in lysates from neuronal cell lines overexpressing αS. This activity is dependent on copper bound to αS as a cofactor and NADH as an electron donor. Overexpression of α-synuclein by cells significantly increases the percentage of iron (II) in cells. The common disease mutations associated with increased susceptibility to PD show differences in activity or iron (II) levels. This discovery may well provide new therapeutic targets for PD and Lewy body dementias.
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spelling pubmed-30184222011-01-19 Alpha-Synuclein Is a Cellular Ferrireductase Davies, Paul Moualla, Dima Brown, David R. PLoS One Research Article α-synuclein (αS) is a cellular protein mostly known for the association of its aggregated forms with a variety of diseases that include Parkinson's disease and Dementia with Lewy Bodies. While the role of αS in disease is well documented there is currently no agreement on the physiological function of the normal isoform of the protein. Here we provide strong evidence that αS is a cellular ferrireductase, responsible for reducing iron (III) to bio available iron (II). The recombinant form of the protein has a V(Max) of 2.72 nmols/min/mg and K(m) 23 µM. This activity is also evident in lysates from neuronal cell lines overexpressing αS. This activity is dependent on copper bound to αS as a cofactor and NADH as an electron donor. Overexpression of α-synuclein by cells significantly increases the percentage of iron (II) in cells. The common disease mutations associated with increased susceptibility to PD show differences in activity or iron (II) levels. This discovery may well provide new therapeutic targets for PD and Lewy body dementias. Public Library of Science 2011-01-10 /pmc/articles/PMC3018422/ /pubmed/21249223 http://dx.doi.org/10.1371/journal.pone.0015814 Text en Davies et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Davies, Paul
Moualla, Dima
Brown, David R.
Alpha-Synuclein Is a Cellular Ferrireductase
title Alpha-Synuclein Is a Cellular Ferrireductase
title_full Alpha-Synuclein Is a Cellular Ferrireductase
title_fullStr Alpha-Synuclein Is a Cellular Ferrireductase
title_full_unstemmed Alpha-Synuclein Is a Cellular Ferrireductase
title_short Alpha-Synuclein Is a Cellular Ferrireductase
title_sort alpha-synuclein is a cellular ferrireductase
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3018422/
https://www.ncbi.nlm.nih.gov/pubmed/21249223
http://dx.doi.org/10.1371/journal.pone.0015814
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