Rapid genotyping using pyrene-perylene locked nucleic acid complexes.

T Santhosh Kumar, Anna Myznikova, Evgeniya Samokhina, Irina Kira Astakhova
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Abstract

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.

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利用芘-过烯锁定核酸复合物快速进行基因分型。
我们开发了一种检测单链 DNA 和 RNA 的方法,该方法基于连接到短 LNA/DNA 探针上的新型芘-珀烯 FRET 对。该检测方法基于三种荧光 LNA/DNA 报告链组合与目标 DNA/RNA 结合后的比率发射。连接到 2'-amino-LNA 第 4 位 2'-amino 基团上的芘荧光团的特定几何形状首次实现了有效利用偶极-偶极定向参数,通过 FRET 检测核酸靶标中的单核苷酸多态性 (SNP)。利用新型探针,SNP 检测具有大斯托克斯位移(115 nm)、高荧光量子产率和低目标检测限值(< 5 nM)等优势。对高度多态的 HIV Pol cDNA 和 RNA 片段进行快速准确的基因分型证明了新型芘-珀烯 FRET 对在成像和临床诊断等方面广泛应用的可能性。
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