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Rapid genotyping using pyrene−perylene locked nucleic acid complexes

机译:使用pyr-per锁定的核酸复合物进行快速基因分型

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摘要

We have developed an assay for single strand DNA and RNA detection which is based on novel pyrene−perylene FRET pairs attached to short LNA/DNA probes. The assay is based on ratiometric emission upon binding of target DNA/RNA by three combinations of fluorescent LNA/DNA reporter strands. Specific geometry of the pyrene fluorophore attached to the 2′-amino group of 2′-amino-LNA in position 4 allows for the first time to efficiently utilize dipole−dipole orientation parameter for sensing of single-nucleotide polymorphisms (SNPs) in nucleic acid targets by FRET. Using novel probes, SNP detection is achieved with advantages of large Stokes shift (115 nm), high fluorescence quantum yields and low limit of target detection values (< 5 nM). Rapid and accurate genotyping of highly polymorphic HIV Pol cDNA and RNA fragments performed herein proves the possibility for broad application of the novel pyrene−perylene FRET pairs, e.g., in imaging and clinical diagnostics.
机译:我们已经开发了一种检测单链DNA和RNA的方法,该方法基于与短LNA / DNA探针相连的新型pyr-per FRET对。该测定基于荧光LNA / DNA报告链的三种组合在结合靶DNA / RNA时的比率发射。在位置4上连接到2'-氨基-LNA的2'-氨基的荧光团的特定几何形状首次允许有效利用偶极子-偶极子定向参数来检测核酸中的单核苷酸多态性(SNP) FRET的目标。使用新型探针可以实现SNP检测,其斯托克斯位移(115 nm)大,荧光量子产率高,目标检测值的下限低(<5 nM)。本文进行的高度多态性HIV Pol cDNA和RNA片段的快速,准确的基因分型证明了将新型pyr-− FRET对广泛应用的可能性,例如,在成像和临床诊断中。

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