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Identification of key structural features of the elusive Cu–Aβ complex that generates ROS in Alzheimer’s disease
Oxidative stress is linked to the etiology of Alzheimer’s disease (AD), the most common cause of dementia in the elderly. Redox active metal ions such as copper catalyze the production of Reactive Oxygen Species (ROS) when bound to the amyloid-β (Aβ) peptide encountered in AD. We propose that this r...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Royal Society of Chemistry
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5613283/ https://www.ncbi.nlm.nih.gov/pubmed/28970897 http://dx.doi.org/10.1039/c7sc00809k |
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author | Cheignon, Clémence Jones, Megan Atrián-Blasco, Elena Kieffer, Isabelle Faller, Peter Collin, Fabrice Hureau, Christelle |
author_facet | Cheignon, Clémence Jones, Megan Atrián-Blasco, Elena Kieffer, Isabelle Faller, Peter Collin, Fabrice Hureau, Christelle |
author_sort | Cheignon, Clémence |
collection | PubMed |
description | Oxidative stress is linked to the etiology of Alzheimer’s disease (AD), the most common cause of dementia in the elderly. Redox active metal ions such as copper catalyze the production of Reactive Oxygen Species (ROS) when bound to the amyloid-β (Aβ) peptide encountered in AD. We propose that this reaction proceeds through a low-populated Cu–Aβ state, denoted the “catalytic in-between state” (CIBS), which is in equilibrium with the resting state (RS) of both Cu(i)–Aβ and Cu(ii)–Aβ. The nature of this CIBS is investigated in the present work. We report the use of complementary spectroscopic methods (X-ray absorption spectroscopy, EPR and NMR) to characterize the binding of Cu to a wide series of modified peptides in the RS. ROS production by the resulting Cu–peptide complexes was evaluated using fluorescence and UV-vis based methods and led to the identification of the amino acid residues involved in the Cu–Aβ CIBS species. In addition, a possible mechanism by which the ROS are produced is also proposed. These two main results are expected to affect the current vision of the ROS production mechanism by Cu–Aβ but also in other diseases involving amyloidogenic peptides with weakly structured copper binding sites. |
format | Online Article Text |
id | pubmed-5613283 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-56132832017-10-02 Identification of key structural features of the elusive Cu–Aβ complex that generates ROS in Alzheimer’s disease Cheignon, Clémence Jones, Megan Atrián-Blasco, Elena Kieffer, Isabelle Faller, Peter Collin, Fabrice Hureau, Christelle Chem Sci Chemistry Oxidative stress is linked to the etiology of Alzheimer’s disease (AD), the most common cause of dementia in the elderly. Redox active metal ions such as copper catalyze the production of Reactive Oxygen Species (ROS) when bound to the amyloid-β (Aβ) peptide encountered in AD. We propose that this reaction proceeds through a low-populated Cu–Aβ state, denoted the “catalytic in-between state” (CIBS), which is in equilibrium with the resting state (RS) of both Cu(i)–Aβ and Cu(ii)–Aβ. The nature of this CIBS is investigated in the present work. We report the use of complementary spectroscopic methods (X-ray absorption spectroscopy, EPR and NMR) to characterize the binding of Cu to a wide series of modified peptides in the RS. ROS production by the resulting Cu–peptide complexes was evaluated using fluorescence and UV-vis based methods and led to the identification of the amino acid residues involved in the Cu–Aβ CIBS species. In addition, a possible mechanism by which the ROS are produced is also proposed. These two main results are expected to affect the current vision of the ROS production mechanism by Cu–Aβ but also in other diseases involving amyloidogenic peptides with weakly structured copper binding sites. Royal Society of Chemistry 2017-07-01 2017-05-04 /pmc/articles/PMC5613283/ /pubmed/28970897 http://dx.doi.org/10.1039/c7sc00809k Text en This journal is © The Royal Society of Chemistry 2017 https://creativecommons.org/licenses/by-nc/3.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial 3.0 Unported License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Chemistry Cheignon, Clémence Jones, Megan Atrián-Blasco, Elena Kieffer, Isabelle Faller, Peter Collin, Fabrice Hureau, Christelle Identification of key structural features of the elusive Cu–Aβ complex that generates ROS in Alzheimer’s disease |
title | Identification of key structural features of the elusive Cu–Aβ complex that generates ROS in Alzheimer’s disease
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title_full | Identification of key structural features of the elusive Cu–Aβ complex that generates ROS in Alzheimer’s disease
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title_fullStr | Identification of key structural features of the elusive Cu–Aβ complex that generates ROS in Alzheimer’s disease
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title_full_unstemmed | Identification of key structural features of the elusive Cu–Aβ complex that generates ROS in Alzheimer’s disease
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title_short | Identification of key structural features of the elusive Cu–Aβ complex that generates ROS in Alzheimer’s disease
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title_sort | identification of key structural features of the elusive cu–aβ complex that generates ros in alzheimer’s disease |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5613283/ https://www.ncbi.nlm.nih.gov/pubmed/28970897 http://dx.doi.org/10.1039/c7sc00809k |
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