Chasing the Elusive “In‐Between” State of the Copper‐Amyloid β Complex by X‐ray Absorption through Partial Thermal Relaxation after Photoreduction

Author:

Falcone Enrico1ORCID,Nobili Germano23ORCID,Okafor Michael1ORCID,Proux Olivier4ORCID,Rossi Giancarlo235ORCID,Morante Silvia23ORCID,Faller Peter16ORCID,Stellato Francesco23ORCID

Affiliation:

1. Institut de Chimie (UMR 7177) University of Strasbourg, CNRS 4 Rue Blaise Pascal 67081 Strasbourg France

2. Università di Roma Tor Vergata, Via della Ricerca Scientifica 00133 Roma Italy

3. INFN, Sezione di Roma Tor Vergata, Via della Ricerca Scientifica 00133 Roma Italy

4. Observatoire des Sciences de l'Univers de Grenoble, UMS 832 CNRS-Université Grenoble Alpes 38041 Grenoble France

5. Centro Fermi, Museo Storico della Fisica e Centro Studi e Ricerche Enrico Fermi Via Panisperna 89a 00184 Roma Italy

6. Institut Universitaire de France (IUF) 1 rue Descartes 75231 Paris France

Abstract

AbstractThe redox activity of Cu ions bound to the amyloid‐β (Aβ) peptide is implicated as a source of oxidative stress in the context of Alzheimer's disease. In order to explain the efficient redox cycling between CuII‐Aβ (distorted square‐pyramidal) and CuI‐Aβ (digonal) resting states, the existence of a low‐populated “in‐between” state, prone to bind Cu in both oxidation states, has been postulated. Here, we exploited the partial X‐ray induced photoreduction at 10 K, followed by a thermal relaxation at 200 K, to trap and characterize by X‐ray Absorption Spectroscopy (XAS) a partially reduced Cu‐Aβ1–16 species different from the resting states. Remarkably, the XAS spectrum is well‐fitted by a previously proposed model of the “in‐between” state, hence providing the first direct spectroscopic characterization of an intermediate state. The present approach could be used to explore and identify the catalytic intermediates of other relevant metal complexes.

Funder

Instituto Nazionale di Fisica Nucleare

Agence Nationale de la Recherche

Publisher

Wiley

Subject

General Medicine

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