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Direct Molecular Detection of Nucleic Acids by Fluorescence Signal Amplification

机译:通过荧光信号放大直接分子检测核酸

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摘要

An integrated PCR-free DNA sensor, which combines a sequence-specific receptor, an optical polymeric transducer, and an intrinsic fluorescence amplification mechanism, is reported. This sensor is based on the different conformations adopted by a cationic polythiophene when electrostatically bound to ss-DNA or ds-DNA, and on the efficient and fast energy transfer between the resulting fluorescent polythiophene/ds-DNA complex and neighboring fluorophores attached to ss-DNA probes. This molecular system allows the detection of only five molecules in 3 mL of an aqueous solution, or 3 zM, in 5 min. Moreover, this work demonstrates, for the first time, the direct detection of single nucleotide polymorphisms (SNPs) from clinical samples in only a few minutes, without the need for nucleic acid amplification.
机译:报道了一种集成了无PCR的DNA传感器,该传感器结合了序列特异性受体,光学聚合物换能器和固有的荧光放大机制。该传感器基于静电结合到ss-DNA或ds-DNA上的阳离子聚噻吩所采用的不同构象,以及所得的荧光聚噻吩/ ds-DNA复合物与附着于ss-DNA的邻近荧光团之间的高效快速能量转移。 DNA探针。该分子系统仅需5分钟即可检测到3 mL水溶液或3 zM中的五个分子。此外,这项工作首次证明了仅需几分钟即可直接从临床样品中直接检测单核苷酸多态性(SNP),而无需进行核酸扩增。

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