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Quantitative imaging and high-throughput analysis of RNA in living cells using molecular-beacon conjugates.

机译:使用分子信标结合物对活细胞中RNA进行定量成像和高通量分析。

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摘要

Variations in gene expression are commonly considered the major determinants for dictating cell behavior. Accordingly, methods to measure gene expression, such as reverse-transcriptase (RT) PCR and DNA microarrays, have proven to be invaluable in regards to understanding cell regulatory processes and disease mechanisms. However, these methods generally provide only the relative change in gene expression for a population of cells with limited spatial-temporal information. We hypothesize that in order to acquire a more complete gene expression profile, a molecular imaging approach must be developed to allow for the absolute quantification of gene expression in single living cells.;We have developed a novel molecular imaging probe, Quantitative Molecular Beacon (QMB), that allows for the absolute quantification of gene expression in single living cells with spatial and temporal resolution. Analogous to conventional MBs, QMBs consist of a hairpin-forming antisense oligonucleotide labeled with a reporter fluorophore and a quencher. Furthermore, QMBs are labeled with a second optically distinct "reference" dye/nanoparticle that remains unquenched regardless of the probe configuration. The reference signal allowed us to determine the intracellular distribution of QMBs, while the fluorescence ratio of the reporter dye to the reference dye (Freporter/Freference) provided us with a measure of the extent of probe hybridization. By comparing these QMB signals in single living cells with standardization curves constructed in vitro, we were able to obtain absolute measurements of RNA in single living cells.;Additionally, we developed a method for the efficient cytosolic delivery of QMBs into living cells with low cytotoxicity. This allowed QMBs to be utilized for the high-throughput detection of gene expression via flow cytometry. With further refinement of the QMB design, it is envisioned that QMBs will become a valuable tool for diagnosing genetic abnormalities.
机译:基因表达的变化通常被认为是决定细胞行为的主要决定因素。因此,已经证明测量基因表达的方法,例如逆转录酶(RT)PCR和DNA微阵列,对于理解细胞调节过程和疾病机制是非常有价值的。但是,这些方法通常只为时空信息有限的细胞群体提供基因表达的相对变化。我们假设为了获得更完整的基因表达谱,必须开发一种分子成像方法以对单个活细胞中的基因表达进行绝对定量。;我们开发了一种新型分子成像探针,定量分子信标(QMB) ),从而可以以空间和时间分辨率对单个活细胞中的基因表达进行绝对定量。类似于常规MB,QMB由形成发夹的反义寡核苷酸组成,所述寡核苷酸用报告荧光团和猝灭剂标记。此外,QMB用第二种光学上不同的“参考”染料/纳米粒子标记,无论探针的配置如何,该染料/纳米粒子都不会被淬灭。参考信号使我们能够确定QMB的细胞内分布,而报告染料与参考染料的荧光比率(Freporter / Freference)为我们提供了探针杂交程度的量度。通过将单个活细胞中的这些QMB信号与体外构建的标准化曲线进行比较,我们能够获得单个活细胞中RNA的绝对测量值;此外,我们开发了一种将QMBs有效地溶质递送到低细胞毒性的活细胞中的方法。这使得QMB可以通过流式细胞仪用于基因表达的高通量检测。随着QMB设计的进一步完善,可以预见QMB将成为诊断遗传异常的有价值的工具。

著录项

  • 作者

    Chen, Antony Kuang-Shih.;

  • 作者单位

    University of Pennsylvania.;

  • 授予单位 University of Pennsylvania.;
  • 学科 Engineering Biomedical.
  • 学位 Ph.D.
  • 年度 2008
  • 页码 271 p.
  • 总页数 271
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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