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Copper Sources for Sod1 Activation

Copper ions (i.e., copper) are a critical part of several cellular processes, but tight regulation of copper levels and trafficking are required to keep the cell protected from this highly reactive transition metal. Cu, Zn superoxide dismutase (Sod1) protects the cell from the accumulation of radica...

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Detalles Bibliográficos
Autores principales: Boyd, Stefanie D., Ullrich, Morgan S., Skopp, Amelie, Winkler, Duane D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7346115/
https://www.ncbi.nlm.nih.gov/pubmed/32517371
http://dx.doi.org/10.3390/antiox9060500
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author Boyd, Stefanie D.
Ullrich, Morgan S.
Skopp, Amelie
Winkler, Duane D.
author_facet Boyd, Stefanie D.
Ullrich, Morgan S.
Skopp, Amelie
Winkler, Duane D.
author_sort Boyd, Stefanie D.
collection PubMed
description Copper ions (i.e., copper) are a critical part of several cellular processes, but tight regulation of copper levels and trafficking are required to keep the cell protected from this highly reactive transition metal. Cu, Zn superoxide dismutase (Sod1) protects the cell from the accumulation of radical oxygen species by way of the redox cycling activity of copper in its catalytic center. Multiple posttranslational modification events, including copper incorporation, are reliant on the copper chaperone for Sod1 (Ccs). The high-affinity copper uptake protein (Ctr1) is the main entry point of copper into eukaryotic cells and can directly supply copper to Ccs along with other known intracellular chaperones and trafficking molecules. This review explores the routes of copper delivery that are utilized to activate Sod1 and the usefulness and necessity of each.
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spelling pubmed-73461152020-07-14 Copper Sources for Sod1 Activation Boyd, Stefanie D. Ullrich, Morgan S. Skopp, Amelie Winkler, Duane D. Antioxidants (Basel) Review Copper ions (i.e., copper) are a critical part of several cellular processes, but tight regulation of copper levels and trafficking are required to keep the cell protected from this highly reactive transition metal. Cu, Zn superoxide dismutase (Sod1) protects the cell from the accumulation of radical oxygen species by way of the redox cycling activity of copper in its catalytic center. Multiple posttranslational modification events, including copper incorporation, are reliant on the copper chaperone for Sod1 (Ccs). The high-affinity copper uptake protein (Ctr1) is the main entry point of copper into eukaryotic cells and can directly supply copper to Ccs along with other known intracellular chaperones and trafficking molecules. This review explores the routes of copper delivery that are utilized to activate Sod1 and the usefulness and necessity of each. MDPI 2020-06-07 /pmc/articles/PMC7346115/ /pubmed/32517371 http://dx.doi.org/10.3390/antiox9060500 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Boyd, Stefanie D.
Ullrich, Morgan S.
Skopp, Amelie
Winkler, Duane D.
Copper Sources for Sod1 Activation
title Copper Sources for Sod1 Activation
title_full Copper Sources for Sod1 Activation
title_fullStr Copper Sources for Sod1 Activation
title_full_unstemmed Copper Sources for Sod1 Activation
title_short Copper Sources for Sod1 Activation
title_sort copper sources for sod1 activation
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7346115/
https://www.ncbi.nlm.nih.gov/pubmed/32517371
http://dx.doi.org/10.3390/antiox9060500
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