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A Nonemissive Iridium(lll) Complex That Specifically Lights-Up the Nuclei of Living Cells

机译:一种非发光铱(III)配合物,特别点亮了活细胞的核

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摘要

A nonemissive cyclometalated iridium(Ⅲ) solvent complex, without conjugation with a cell-penetrating molecular transporter, [Ir(ppy)_2(DMSO)_2]+PF-6(LIr1), has been developed as a first reaction-based fluorescence-turn-on agent for the nuclei of living cells. LIrl can rapidly and selectively light-up the nuclei of living cells over fixed cells, giving rise to a significant luminescence enhancement (200-fold), and shows very low cytotoxicity at the imaging concentration (incubation time < 10 min, LIrl concentration 10/uM). More importantly, in contrast to the reported nuclear stains that are based on luminescence enhancement through interaction with nucleic acids, complex LIrl as a nuclear stain has a reaction-based mode of action, which relies on its rapid reaction with histidine/histidine-containing proteins. Cellular uptake of LIrl has been investigated in detail under different conditions, such as at various temperatures, with hypertonic treatment, and in the presence of metabolic and endocytic inhibitors. The results have indicated that LIrl permeates the outer and nuclear membranes of living cells through an energy-dependent entry pathway within a few minutes. As determined by an inductively coupled plasma atomic emission spectroscopy (ICP-AEC), LIrl is accumulated in the nuclei of living cells and converted into an intensely emissive adduct. Such novel reaction-based nuclear staining for visualizing exclusively the nuclei of living cells with a significant luminescence enhancement may extend the arsenal of currently available fluorescent stains for specific staining of cellular compartments.
机译:一种不与细胞穿透分子转运蛋白[Ir(ppy)_2(DMSO)_2] + PF-6(LIr1)结合的无辐射环金属化铱(Ⅲ)溶剂配合物,已被开发出来。活细胞核的开启剂。 LIrl可以快速且有选择地照亮固定细胞上的活细胞核,从而产生显着的发光增强(200倍),并且在成像浓度下(显示时间<10分钟,LIrl浓度为10 /嗯)更重要的是,与已报道的基于通过与核酸相互作用增强发光的核染色剂相比,作为核染色剂的复杂LIrl具有基于反应的作用方式,这取决于其与组氨酸/含组氨酸的蛋白质的快速反应。已经在不同条件下,例如在各种温度下,通过高渗处理,并且在存在代谢和内吞抑制剂的情况下,详细研究了LIrl的细胞摄取。结果表明,LIr1在几分钟内通过能量依赖性进入途径渗透了活细胞的外膜和核膜。如通过电感耦合等离子体原子发射光谱法(ICP-AEC)所确定的,LIr1积累在活细胞的核中并转化为强发射加合物。这种新颖的基于反应的核染色法,可以专门观察具有显着发光增强作用的活细胞的核,可以扩展当前可用的荧光染色剂的库,用于细胞区的特异性染色。

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  • 来源
    《Journal of the American Chemical Society》 |2011年第29期|p.11231-11239|共9页
  • 作者单位

    Joint Center of Biomedical Imaging (BMI) of Department of Chemistry & Institute of Biomedical Science & Cancer Hospital, Laboratory of Advanced Materials, Fudan University, Shanghai 200433, P. R. China;

    Joint Center of Biomedical Imaging (BMI) of Department of Chemistry & Institute of Biomedical Science & Cancer Hospital, Laboratory of Advanced Materials, Fudan University, Shanghai 200433, P. R. China;

    Joint Center of Biomedical Imaging (BMI) of Department of Chemistry & Institute of Biomedical Science & Cancer Hospital, Laboratory of Advanced Materials, Fudan University, Shanghai 200433, P. R. China;

    Joint Center of Biomedical Imaging (BMI) of Department of Chemistry & Institute of Biomedical Science & Cancer Hospital, Laboratory of Advanced Materials, Fudan University, Shanghai 200433, P. R. China;

    Joint Center of Biomedical Imaging (BMI) of Department of Chemistry & Institute of Biomedical Science & Cancer Hospital, Laboratory of Advanced Materials, Fudan University, Shanghai 200433, P. R. China;

    Joint Center of Biomedical Imaging (BMI) of Department of Chemistry & Institute of Biomedical Science & Cancer Hospital, Laboratory of Advanced Materials, Fudan University, Shanghai 200433, P. R. China;

  • 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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