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A homogeneous europium cryptate-based assay for the diagnosis of mutations by time-resolved fluorescence resonance energy transfer

机译:基于均相euro的一种基于时间分辨荧光共振能量转移的突变诊断方法

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摘要

Oligonucleotide ligation assay (OLA) is considered to be a very useful methodology for the detection and characterization of mutations, particularly for clinical purposes. The fluorescence resonance energy transfer between a fluorescent donor and a suitable fluorophore as acceptor has been applied in the past to several scientific fields. This technique is well adapted to nucleic acid analysis such as DNA sequencing, DNA hybridization and polymerase chain reaction. We describe here a homogeneous format based on the use of a rare earth cryptate label as donor: tris-bipyridine-Eu3+. The long-lived fluorescence of this label makes it possible to reach a high sensitivity by using a time-resolved detection mode. A non-radiative energy transfer technology, known as time-resolved amplification of cryptate emission (TRACE(R)) characterized by a temporal and spectral selectivity has been developed. The TRACE(R) detection of characterized single nucleotide polymorphism using the OLA for allelic discrimination is proposed. We demonstrate the potentialities of this OLA-TRACE(R) methodology through the analysis of K-ras oncogene point mutations.
机译:寡核苷酸连接测定法(OLA)被认为是检测和表征突变,特别是用于临床目的的非常有用的方法。过去已经将荧光供体和合适的荧光团作为受体之间的荧光共振能量转移应用于一些科学领域。该技术非常适合核酸分析,例如DNA测序,DNA杂交和聚合酶链反应。我们在此基于使用稀土加密标记作为供体的tris-bipyridine-Eu3 +来描述均匀格式。该标记的长寿命荧光使得可以通过使用时间分辨检测模式来达到高灵敏度。已经开发了一种非辐射能量转移技术,称为时间分辨的隐秘发射放大(TRACE),其特征在于时间和光谱的选择性。提出了使用OLA进行等位基因识别的特征单核苷酸多态性的TRACE(R)检测。我们通过分析K-ras癌基因点突变证明了这种OLA-TRACE(R)方法的潜力。

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