Hosseini Morteza, Akbari Azam, Ganjali Mohammad Reza, Dadmehr Mehdi, Rezayan Ali Hossein
Department of Life Science Engineering, Faculty of New Sciences & Technologies, University of Tehran, Tehran, Iran,
J Fluoresc. 2015 Jul;25(4):925-9. doi: 10.1007/s10895-015-1574-5. Epub 2015 May 9.
In this paper, a new approach for microRNA-155 (miRNA-155) detection was described based on the fluorescence quenching of oligonucleotide-templated silver nanoclusters (DNA-AgNCs). The specific DNA scaffold with two different nucleotides fragments were used: one was enriched with a cytosine sequence fragment (C12) that could result in DNA-AgNCs with a high quantum yield via a chemical reduction method, and the other was the probe fragment (5- CUGUUAAUGCUAAUCGUG-3) which could selectively bind to the miRNA-155. Thus, the as-prepared AgNCs could exhibit quenched fluorescence when binding to the target miRNA-155. The fluorescence ratio of the DNA-AgNCs was quenched in a linearly proportional manner to the concentration of the target in the range of 0.2 nM to 30 nM with a detection limit of 0.1 nM.
本文描述了一种基于寡核苷酸模板化银纳米簇(DNA-AgNCs)荧光猝灭的微小RNA-155(miRNA-155)检测新方法。使用了具有两个不同核苷酸片段的特定DNA支架:一个富含胞嘧啶序列片段(C12),通过化学还原法可产生具有高量子产率的DNA-AgNCs;另一个是探针片段(5'-CUGUUAAUGCUAAUCGUG-3'),它可以选择性地与miRNA-155结合。因此,制备的AgNCs与靶标miRNA-155结合时会表现出荧光猝灭。DNA-AgNCs的荧光比率在0.2 nM至30 nM范围内与靶标浓度呈线性比例猝灭,检测限为0.1 nM。