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首页> 外文期刊>Russian journal of bioorganic chemistry >Regulation of Aggregation of Self-Associated Peptides, Including N-Terminal Fragments of the Alzheimer's -Amyloid Peptide, by Nitro Derivatives of Azoloazine
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Regulation of Aggregation of Self-Associated Peptides, Including N-Terminal Fragments of the Alzheimer's -Amyloid Peptide, by Nitro Derivatives of Azoloazine

机译:自相关肽的聚集的调节,包括阿尔茨海默氏蛋白肽的N-末端片段,由氮杂氮杂的硝基衍生物

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摘要

The potential of the nitro compounds of the azoloazine class as regulators of aggregation of natural self-associating peptides was demonstrated by the example of fragments of the Alzheimer -amyloid peptide and the melittin cytolytic peptide from bee venom. Depending on the type of an azoloazine derivative, association of a peptide into insoluble aggregates either occurred or was suppressed up to the peptide aggregates dissolution. The sites and stoichiometry of the azoloazine binding to the examined peptides are determined in the associates. These effects were explained by a unique ability of the azoloazine nitro derivatives to dissociate in aqueous solutions with the formation of a stable aromatic anion with electrostatic affinity to basic amino acid residues of the peptide molecules. This property of nitroazoloazines was used for a test of their ability to regulate the aggregation processes. Therefore, the nitro derivatives of azoloazines are promising inducers or inhibitors of the aggregation of the Alzheimer -amyloid peptide and, possibly, other peptides which can form amyloid deposits.
机译:通过阿尔茨海默蛋白 - 烷肽的片段和来自蜂毒液的蛋白质细胞分解肽的碎片的实例,证明了偶氮嗪类作为天然自相关肽的聚集的调节剂的氮杂化合物的潜力。取决于偶氮嗪衍生物的类型,肽将肽与不溶性聚集体的结合发生或被抑制到肽聚集体溶解。在缔合物中测定偶氮嗪与所检查肽结合的唑唑嗪结合的部位和化学计量。通过氮杂杂嗪硝基衍生物在水溶液中解散的独特能力解释了这些效果,以形成稳定的芳香族的阳性亲和力,肽分子的碱性亲和力。 Nitroazoloozines的这种性质用于测试它们调节聚集过程的能力。因此,氮醌的硝基衍生物是阿尔茨海默聚酰胺肽的聚集的承诺诱导剂或抑制剂,并且可能是可以形成淀粉样沉积物的其他肽。

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