首页> 外文期刊>Journal of the American Chemical Society >Fluorescent BODIPY-Based Zn(II) Complex as a Molecular Probe for Selective Detection of Neurofibrillary Tangles in the Brains of Alzheimer's Disease Patients
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Fluorescent BODIPY-Based Zn(II) Complex as a Molecular Probe for Selective Detection of Neurofibrillary Tangles in the Brains of Alzheimer's Disease Patients

机译:基于荧光BODIPY的Zn(II)配合物作为选择性检测阿尔茨海默氏病患者大脑中神经原纤维缠结的分子探针

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摘要

We have developed a new fluorescent binuclear Zn(II) complex for the detection of neurofibrillary tangles (NFTs) of hyperphosphorylated tau proteins, a representative hallmark of Alzheimer's disease (AD). The probe 1 incorporates a fluorescent BODIPY unit and two Zn(II)-2,2'-dipicolylamine (Dpa) complexes as a binding site for phosphorylated amino acid residues. Using fluorescence titration to evaluate the binding and sensing properties of 1 toward several phosphorylated peptide segments derived from hyperphosphorylated tau protein, we found that 1 binds preferentially to peptides presenting phosphorylated groups at the i and i+4 positions with dissociation constants (K_d) in the micromolar range. Fluorescence titration with an artificially prepared aggregate of the phosphorylated tau protein (p-Tau) revealed that 1 binds strongly to p-Tau (EC_(50) = 9 nM). In contrast, the interactions of 1 were weaker toward artificially prepared aggregates of the nonphosphorylated tau protein (n-Tau; EC_(50) = 80 nM) and Aβ_(1-42) fibrils (EC_(50) = 6_(50) nM). Histological imaging of a hippocampus tissue section obtained from an AD patient revealed that 1 fluorescently visualizes deposits of NFTs and clearly discriminates between NFTs and the amyloid plaques assembled from amyloid-β peptides, confirming our strategy toward the rational design of a molecular probe for the selective fluorescence detection of NFTs in brain tissue sections.
机译:我们已经开发了一种新的荧光双核Zn(II)复合物,用于检测高磷酸化tau蛋白的神经原纤维缠结(NFT),这是阿尔茨海默氏病(AD)的代表性标志。探针1结合有荧光BODIPY单元和两个Zn(II)-2,2′-二甲基吡啶胺(Dpa)复合物作为磷酸化氨基酸残基的结合位点。使用荧光滴定法评估1对源自超磷酸化tau蛋白的几个磷酸化肽段的结合和传感特性,我们发现1优先结合在i和i + 4位置上具有磷酸化基团的肽,其解离常数为(K_d)。微摩尔范围。用人工制备的磷酸化tau蛋白(p-Tau)聚集体进行荧光滴定表明1与p-Tau牢固结合(EC_(50)= 9 nM)。相反,对于人工制备的非磷酸化tau蛋白(n-Tau; EC_(50)= 80 nM)和Aβ_(1-42)原纤维(EC_(50)= 6_(50)nM)的聚集体,1的相互作用较弱。 )。从一名AD患者获得的海马组织切片的组织学成像显示,1荧光显示NFT的沉积物并清楚地区分NFT和由淀粉样β肽组装而成的淀粉样斑块,这证实了我们为合理设计选择性分子探针的策略荧光检测脑组织切片中的NFT。

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  • 来源
    《Journal of the American Chemical Society》 |2009年第18期|6543-6548|共6页
  • 作者单位

    Department of Synthetic Chemistry and Biological Chemistry, Graduate School of Engineering, Kyoto University, Katsura campus, Kyoto 615-8510, Japan JST, PRESTO (Life Phenomena and Measurement Analysis), Sanbancho, Chiyodaku, Tokyo 102-0075, Japan;

    Department of Synthetic Chemistry and Biological Chemistry, Graduate School of Engineering, Kyoto University, Katsura campus, Kyoto 615-8510, Japan;

    Department of Synthetic Chemistry and Biological Chemistry, Graduate School of Engineering, Kyoto University, Katsura campus, Kyoto 615-8510, Japan;

    Department of Synthetic Chemistry and Biological Chemistry, Graduate School of Engineering, Kyoto University, Katsura campus, Kyoto 615-8510, Japan;

    CNRS-Universite de Lille 1, UMR 8576, USTL, Avenue de Mandeleiev, 59655 Villeneuve d'Ascq Cedex, France;

    Department of Synthetic Chemistry and Biological Chemistry, Graduate School of Engineering, Kyoto University, Katsura campus, Kyoto 615-8510, Japan CNRS-Universite de Lille 1, UMR 8576, USTL, Avenue de Mandeleiev, 59655 Villeneuve d'Ascq Cedex, France;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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  • 入库时间 2022-08-18 03:16:53

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