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Exploring the differences between mouse mAβ_(1-42) and human hAβ(1-42) for Alzheimer's disease related properties and neuronal cytotoxicity

机译:探索小鼠mAβ_(1-42)和人类hAβ(1-42)之间的阿尔茨海默氏病相关特性和神经元细胞毒性的差异

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摘要

The differences between mouse mAβ_(1-42) and human hAβ_(1-42). Explored using CD and fluorescence spectroscopy, transmission electron microscopy, ROS fluorescent assay, and neuronal cell viability, revealed that mAβ_(1-42) as a three-site mutant (R5G, Y10F and H13R) of hAβ_(1-42) altered the metal (copper and zinc) binding sites, reduced the proneness to form ss-sheet structures and aggregated fibrils, alleviated the generation of ROS, and decreased the cytotoxicity, in contrast to hAβ_(1-42).
机译:小鼠mAβ_(1-42)和人类hAβ_(1-42)之间的差异。使用CD和荧光光谱,透射电镜,ROS荧光测定和神经元细胞活力进行了探索,发现作为hAβ_(1-42)的三位突变体(R5G,Y10F和H13R)的mAβ_(1-42)改变了与hAβ_(1-42)相比,金属(铜和锌)的结合位点减少了形成ss-sheet结构和聚集的原纤维的倾向,减轻了ROS的产生,并降低了细胞毒性。

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  • 来源
    《Chemical Communications》 |2013年第52期|5865-5867|共3页
  • 作者单位

    Department of Chemistry and Institutes of Biomedical Sciences, Fudan University, Shanghai 200433, China;

    Department of Chemistry and Institutes of Biomedical Sciences, Fudan University, Shanghai 200433, China;

    Department of Chemistry and Institutes of Biomedical Sciences, Fudan University, Shanghai 200433, China;

    State Key Laboratory of Medical Neurobiology, Shanghai Medical College of Fudan University, Shanghai, China;

    State Key Laboratory of Medical Neurobiology, Shanghai Medical College of Fudan University, Shanghai, China;

    Department of Chemistry and Institutes of Biomedical Sciences, Fudan University, Shanghai 200433, China;

    Department of Chemistry and Institutes of Biomedical Sciences, Fudan University, Shanghai 200433, China;

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