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基于超灵敏荧光的核酸检测方法:迈向无扩增的遗传分析。

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

机构信息

Department of Chemistry, University of Cambridge, Lensfield Road, Cambridge, UK CB2 1EW.

出版信息

Chem Commun (Camb). 2011 Apr 7;47(13):3717-35. doi: 10.1039/c0cc04215c. Epub 2011 Jan 31.

Abstract

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.

摘要

实时 PCR 是目前核酸检测的主要手段,为法医学、即时诊断和生物恐怖主义制剂检测等领域提供了支持。尽管其用途广泛,但在第二代和第三代 DNA 测序技术的启发下,在单分子荧光光谱学、纳米技术和微制造技术进步的推动下,人们仍在继续寻找新的检测方法。这些新方法有望实现无需酶扩增即可直接检测核酸。在这篇专题文章中,我们从化学角度介绍了这个多学科领域,介绍了单分子检测的概念,然后重点介绍了适合通过超灵敏荧光光谱法产生可检测信号的标签和探针化学的选择。最后,我们讨论了将这些检测平台集成到“样品进-结果出”仪器中所需要的进一步发展,使这些仪器能够在数分钟内检测到多个目标序列。

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