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Fluorogenic Dendrons with Multiple Donor Chromophores as Bright Genetically Targeted and Activated Probes

机译:具有多个供体发色团的荧光树突作为明亮的遗传靶向和激活探针。

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摘要

We have developed a class of dendron-based fluorogenic dyes (termed dyedrons) comprised of multiple cyanine (Cy3) donors coupled to a single malachite green (MG) acceptor that fluoresce only when the MG is noncovalently but specifically bound to a cognate single chain antibody (scFv). These cell-impermeant dydrons exploit efficient intramolecular energy transfer from Cy3 donors to stoichiometrically amplify the fluorescence of MG chromophores that are activated by binding to the scFv. These chromophore enhancements, coupled with our optimized scFv, can significantly increase fluorescence emission generated by the dyedron/ scFv complex to brightness levels several-fold greater than that for single fluorescent proteins and targeted small molecule fluorophores. Efficient intramolecular quenching of free dyedrons enables sensitive homogeneous (no wash) detection under typical tissue culture conditions, with undetectable nonspecific activation.
机译:我们已经开发出了一类基于树枝状的荧光染料(称为染料),由多个花菁(Cy3)供体与单个孔雀石绿(MG)受体偶联,仅当MG非共价但特异性结合同源单链抗体时才发荧光(scFv)。这些不渗透细胞的中子利用来自Cy3供体的有效分子内能量转移,以化学计量方式放大了通过与scFv结合而激活的MG生色团的荧光。这些生色团的增强,加上我们优化的scFv,可以显着增加染料/ scFv复合物产生的荧光发射,使其亮度水平比单个荧光蛋白和目标小分子荧光团的亮度水平高几倍。游离染料的有效分子内淬灭可以在典型的组织培养条件下进行灵敏的均相(无需洗涤)检测,并且具有不可检测的非特异性激活。

著录项

  • 来源
    《Journal of the American Chemical Society》 |2010年第32期|p.11103-11109|共7页
  • 作者单位

    Carnegie Mellon University, Molecular Biosensors;

    rnCarnegie Mellon University, Molecular Biosensors;

    rnCarnegie Mellon University, Molecular Biosensors Waitt Advanced Biophotonics Center, Salk Institute for Biological Studies, 10010 North Torrey Pines Road, La Jo11a, CA 92037;

    rnCarnegie Mellon University, Molecular Biosensors Imaging Center, Department of Chemistry, 4400 Fifth Avenue, Pittsburgh, Pennsylvania 15213;

  • 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);
  • 原文格式 PDF
  • 正文语种 eng
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  • 入库时间 2022-08-18 03:15:45

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