Issue 10, 2016

Metal-catalyzed oxidation of Aβ and the resulting reorganization of Cu binding sites promote ROS production

Abstract

In the context of Alzheimer's disease (AD), the production of HO˙ by copper–amyloid beta (Aβ) in the presence of ascorbate is known to be deleterious for the Aβ peptide itself and also for the surrounding molecules, thus establishing a direct link between AD and oxidative stress. The metal-catalyzed oxidation (MCO) of Aβ primarily targets the residues involved in copper coordination during HO˙ production. In the present work, we demonstrate that the oxidative damage undergone by Aβ during MCO lead to a change in copper coordination, with enhanced catalytic properties that increases the rates of ascorbate consumption and HO˙ production, and the amount of HO˙ released by the system. This phenomenon is observed after the peptide has been sufficiently oxidized.

Graphical abstract: Metal-catalyzed oxidation of Aβ and the resulting reorganization of Cu binding sites promote ROS production

Supplementary files

Article information

Article type
Paper
Submitted
05 Jul 2016
Accepted
24 Aug 2016
First published
25 Aug 2016
This article is Open Access
Creative Commons BY-NC license

Metallomics, 2016,8, 1081-1089

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