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A Fluorescence-Based G-Quadruplex DNA Cleavage Assay

机译:基于荧光的G-四链体DNA裂解测定

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摘要

We describe a fluorescence-based G-quadruplex DNA cleavage assay based on intramolecular G-quadruplex-forming 5',3'-dual labeled oligonucleotides. By utilizing the difference in fluorescence emission spectra between an intact and cleaved quadruplex, the extent of G-quadruplex cleavage can be determined for a range of agents including hydroxyl radical, photo-activated porphyrin TMPyP4, and the oxo-metalloporphyrin Mn(=O)TMPyP4. This assay has been adapted to 96-well format for rapid screening, and the cleavage reaction samples can be subsequently directly analyzed by PAGE with fluorescence visualization. Agents that selectively cleave G-quadruplexes may serve as valuable probes for elucidating the formation and resolution of these structures in cells or as therapeutic agents. This assay should aid in identifying G-quadruplex cleavage agents for these various applications.
机译:我们描述了基于分子内G-四链体形成5',3'-双标记寡核苷酸的基于荧光的G-四链体DNA裂解测定。通过利用完整和裂解的四链体之间荧光发射光谱的差异,可以确定包括羟基自由基,光活化卟啉TMPyP4和氧代金属卟啉Mn(= O)在内的一系列试剂的G-四链体裂解程度。 TMPyP4。该测定方法已适应96孔格式,可进行快速筛选,随后可通过PAGE和荧光可视化直接分析裂解反应样品。选择性切割G-四链体的试剂可作为有价值的探针,用于阐明细胞中这些结构的形成和分解或作为治疗剂。该测定法应有助于鉴定用于这些各种应用的G-四链体裂解剂。

著录项

  • 来源
    《Frontiers in nucleic acids.》|2010年|p.13-32|共20页
  • 会议地点 New Orleans LA(US);New Orleans LA(US)
  • 作者单位

    Department of Chemistry and Biochemistry, University of Texas at Austin, Austin, TX, 78712 USA;

    Department of Chemistry and Biochemistry, University of Texas at Austin, Austin, TX, 78712 USA,Division of Medicinal Chemistry, College of Pharmacy, University of Texas at Austin, Austin, TX, 78712 USA;

  • 会议组织
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 核酸;核酸;
  • 关键词

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