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Interaction of iron(II)-heme and artemisinin with a peptide mimic of Plasmodium falciparum HRP-II

机译:铁(II)-血红素和青蒿素与恶性疟原虫HRP-II的肽模拟物的相互作用

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摘要

The interaction of heme or heme-artemisinin adducts (heme-art) with different peptides mimicking repeat sequences of the Histidine-Rich-Protein-II of Plasmodium falciparum (PfHRP-II) was investigated. The pseudo-first order rate constants of the coordination of heme or heme-art onto a histidine rich peptide, used as a mimic of PfHRP-II putative heme binding sequence, are of the same order of magnitude, namely 42 and 14 s(-1), respectively. Despite the intrinsic reactivity of the carbonyl at C10 of heme-art toward a hydroxyl function, a peptide containing a serine or threonine residue does not readily react with heme-art adducts. Therefore, a much higher affinity of heme-art compared to heme toward PfHRP-II, if so, must be induced by a specific interaction or a chemical reaction, these phenomena being both due to the tertiary structure of the parasite protein itself.
机译:研究了血红素或血红素-青蒿素加合物(血红素-art)与模拟恶性疟原虫组氨酸-富蛋白质-II(PfHRP-II)重复序列的不同肽的相互作用。模仿PfHRP-II假定的血红素结合序列的血红素或血红素与富组氨酸肽的配位的伪一级反应速率常数处于相同数量级,即42和14 s(- 1)。尽管血红素艺术的C 10处的羰基具有对羟基官能团的固有反应性,但是含有丝氨酸或苏氨酸残基的肽不容易与血红素艺术的加合物反应。因此,与血红素相比,血红素对PfHRP-II的亲和力要高得多,如果是这样的话,则必须通过特异性相互作用或化学反应来诱导,这些现象都是由于寄生虫蛋白本身的三级结构引起的。

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