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Resistance of Cu(Aβ4 – 16) to Copper Capture by Metallothionein‐3 Supports a Function for the Aβ4 – 42 Peptide as a Synaptic Cu II Scavenger
Author(s) -
Wezynfeld Nina E.,
Stefaniak Ewelina,
Stachucy Kinga,
Drozd Agnieszka,
Płonka Dawid,
Drew Simon C.,
Krężel Artur,
Bal Wojciech
Publication year - 2016
Publication title -
angewandte chemie
Language(s) - English
Resource type - Journals
eISSN - 1521-3757
pISSN - 0044-8249
DOI - 10.1002/ange.201511968
Subject(s) - metallothionein , peptide , copper , chemistry , neuroprotection , scavenger , antioxidant , zinc , pathogenesis , biophysics , biochemistry , biology , neuroscience , immunology , organic chemistry
Aβ4‐42 is a major species of Aβ peptide in the brains of both healthy individuals and those affected by Alzheimer's disease. It has recently been demonstrated to bind Cu II with an affinity approximately 3000 times higher than the commonly studied Aβ1‐42 and Aβ1‐40 peptides, which are implicated in the pathogenesis of Alzheimer's disease. Metallothionein‐3, a protein considered to orchestrate copper and zinc metabolism in the brain and provide antioxidant protection, was shown to extract Cu II from Aβ1‐40 when acting in its native Zn 7 MT‐3 form. This reaction is assumed to underlie the neuroprotective effect of Zn 7 MT‐3 against Aβ toxicity. In this work, we used the truncated model peptides Aβ1‐16 and Aβ4‐16 to demonstrate that the high‐affinity Cu II complex of Aβ4‐16 is resistant to Zn 7 MT‐3 reactivity. This indicates that the analogous complex of the full‐length peptide Cu(Aβ4‐42) will not yield copper to MT‐3 in the brain, thus supporting the concept of a physiological role for Aβ4‐42 as a Cu II scavenger in the synaptic cleft.