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基于荧光银纳米簇的新型无标记微小RNA-155检测

A Novel Label-Free microRNA-155 Detection on the Basis of Fluorescent Silver Nanoclusters.

作者信息

Hosseini Morteza, Akbari Azam, Ganjali Mohammad Reza, Dadmehr Mehdi, Rezayan Ali Hossein

机构信息

Department of Life Science Engineering, Faculty of New Sciences & Technologies, University of Tehran, Tehran, Iran,

出版信息

J Fluoresc. 2015 Jul;25(4):925-9. doi: 10.1007/s10895-015-1574-5. Epub 2015 May 9.

Abstract

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.

摘要

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。

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