Kumar T Santhosh, Myznikova Anna, Samokhina Evgeniya, Astakhova Irina Kira
Nucleic Acid Center; Department of Physics, Chemistry and Pharmacy; University of Southern Denmark; Odense, Denmark ; National Institute of Diabetes and Digestive and Kidney Diseases; National Institutes of Health; Molecular Recognition Section; Bethesda, MD USA.
Artif DNA PNA XNA. 2013 Apr-Jun;4(2):58-68. doi: 10.4161/adna.25903.
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.
我们开发了一种用于单链DNA和RNA检测的分析方法,该方法基于连接到短锁核酸(LNA)/DNA探针上的新型芘-苝荧光共振能量转移(FRET)对。该分析方法基于三种荧光LNA/DNA报告链组合与靶DNA/RNA结合时的比率发射。连接到4位2'-氨基-LNA的2'-氨基基团上的芘荧光团的特定几何结构首次使得能够通过FRET有效利用偶极-偶极取向参数来检测核酸靶标中的单核苷酸多态性(SNP)。使用新型探针,实现了SNP检测,具有大斯托克斯位移(115nm)、高荧光量子产率和低靶标检测限值(<5 nM)等优点。本文对高度多态的HIV Pol cDNA和RNA片段进行的快速准确基因分型证明了新型芘-苝FRET对广泛应用的可能性,例如在成像和临床诊断中。