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A Cu-bis(imidazole) Substrate Intermediate Is the Catalytically Competent Center for Catechol Oxidase Activity of Copper Amyloid-β
Author(s) -
Chiara Bacchella,
Simone Dell’Acqua,
Stefania Nicolis,
Enrico Monzani,
Luigi Casella
Publication year - 2021
Publication title -
inorganic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.348
H-Index - 233
eISSN - 1520-510X
pISSN - 0020-1669
DOI - 10.1021/acs.inorgchem.0c02243
Subject(s) - chemistry , catechol , hydrogen peroxide , imidazole , reactivity (psychology) , copper , redox , superoxide , amine gas treating , catechol oxidase , catalysis , substrate (aquarium) , photochemistry , combinatorial chemistry , stereochemistry , enzyme , inorganic chemistry , organic chemistry , peroxidase , medicine , polyphenol oxidase , oceanography , alternative medicine , pathology , geology
Interaction of copper ions with Aβ peptides alters the redox activity of the metal ion and can be associated with neurodegeneration. Many studies deal with the characterization of the copper binding mode responsible for the reactivity. Oxidation experiments of dopamine and related catechols by copper(II) complexes with the N-terminal amyloid-β peptides Aβ 16 and Aβ 9 , and the Aβ 16 [H6A] and Aβ 16 [H13A] mutant forms, both in their free amine and N-acetylated forms show that efficient reactivity requires the oxygenation of a Cu I -bis(imidazole) complex with a bound substrate. Therefore, the active intermediate for catechol oxidation differs from the proposed "in-between state" for the catalytic oxidation of ascorbate. During the catechol oxidation process, hydrogen peroxide and superoxide anion are formed but give only a minor contribution to the reaction.

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