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Ultrasensitive fluorescence-based methods for nucleic acid detection: towards amplification-free genetic analysis.

机译:基于超灵敏荧光的核酸检测方法:无扩增遗传分析。

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摘要

Real time PCR is the mainstay of current nucleic acid assays, underpinning applications in forensic science, point-of-care diagnostics and detection of bioterrorism agents. Despite its broad utility, the search for new tests continues, inspired by second and third generation DNA sequencing technologies and fuelled by progress in single molecule fluorescence spectroscopy, nanotechnology and microfabrication. These new methods promise the direct detection of nucleic acids without the need for enzymatic amplification. In this feature article, we provide a chemist's perspective on this multidisciplinary area, introducing the concepts of single molecule detection then focussing on the selection of labels and probe chemistry suitable for generating a signal detectable by ultrasensitive fluorescence spectroscopy. Finally, we discuss the further developments that are required to incorporate these detection platforms into integrated 'sample-in-answer-out' instruments, capable of detecting many target sequences in a matter of minutes.
机译:实时PCR是当前核酸测定的主要手段,可支持法医学,即时医疗诊断和生物恐怖分子检测的应用。尽管其用途广泛,但受到第二代和第三代DNA测序技术的启发,并且随着单分子荧光光谱法,纳米技术和微细加工技术的发展,新的测试仍在继续。这些新方法有望直接检测核酸,而无需酶促扩增。在这篇专题文章中,我们提供了化学家对该多学科领域的看法,介绍了单分子检测的概念,然后重点介绍了适用于产生可通过超灵敏荧光光谱检测到的信号的标记物和探针化学物质的选择。最后,我们讨论了将这些检测平台整合到集成的“进出样本”仪器中所需的进一步发展,该仪器能够在几分钟内检测到许多目标序列。

著录项

  • 作者

    Ranasinghe, RT; Brown, T;

  • 作者单位
  • 年度 2011
  • 总页数
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类

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