Dipartimento di Chimica, Università di Pavia, Via Taramelli 12, 27100, Pavia, Italy.
Chemistry. 2016 Nov 14;22(47):16964-16973. doi: 10.1002/chem.201603824. Epub 2016 Oct 13.
The oxidative reactivity of copper complexes with Aβ peptides 1-16 and 1-28 (Aβ16 and Aβ28) against dopamine and related catechols under physiological conditions has been investigated in parallel with the competitive oxidative modification undergone by the peptides. It was found that both Aβ16 and Aβ28 markedly increase the oxidative reactivity of copper(II) towards the catechol compounds, up to a molar ratio of about 4:1 of peptide/copper(II). Copper redox cycling during the catalytic activity induces the competitive modification of the peptide at selected amino acid residues. The main modifications consist of oxidation of His13/14 to 2-oxohistidine and Phe19/20 to ortho-tyrosine, and the formation of a covalent His6-catechol adduct. Competition by the endogenous peptide is rather efficient, as approximately one peptide molecule is oxidized every 10 molecules of 4-methylcatechol.
已对铜配合物与 Aβ 肽 1-16 和 1-28(Aβ16 和 Aβ28)在生理条件下对多巴胺和相关儿茶酚的氧化反应性进行了平行研究,同时还研究了肽所经历的竞争性氧化修饰。结果发现,Aβ16 和 Aβ28 明显增加了铜(II)对儿茶酚化合物的氧化反应性,最高可达约 4:1 的肽/铜(II)摩尔比。在催化活性期间,铜的氧化还原循环诱导肽在选定的氨基酸残基上发生竞争性修饰。主要修饰包括 His13/14 氧化为 2-氧代组氨酸和 Phe19/20 为邻酪氨酸,以及形成共价 His6-儿茶酚加合物。内源性肽的竞争相当有效,因为大约每 10 个 4-甲基儿茶酚分子就会氧化一个肽分子。