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Rather than binding to His residues with a very low K D in Aβ42, Cu 2+ bound to a high- K D , low-affinity site, i.e., Met, coupled to an oxidation-reduction one-electron transfer from the Met S-atom to the Cu(II) ion, is consonant with the mechanism of forming a sulfuranyl free radical on the Met35 residue posited by the Butterfield laboratory as key to initiating lipid peroxidation in AD as described above

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