Quantitative and Multiplexed MicroRNA Sensing in Living Cells Based on Peptide Nucleic Acid and Nano Graphene Oxide (PANGO)

被引:259
作者
Ryoo, Soo-Ryoon [1 ]
Lee, Jieon [1 ]
Yeo, Jinah [2 ,3 ]
Na, Hee-Kyung [4 ]
Kim, Young-Kwan [1 ]
Jang, Hongje [4 ]
Lee, Jung Hyun [3 ]
Han, Sang Woo [4 ]
Lee, Younghoon [4 ]
Kim, Vic Narry [2 ,3 ]
Min, Dal-Hee [1 ,2 ]
机构
[1] Seoul Natl Univ, Dept Chem, Seoul 151747, South Korea
[2] Inst for Basic Sci Korea, Ctr RNA Res, Seoul 151747, South Korea
[3] Seoul Natl Univ, Sch Biol Sci, Seoul 151747, South Korea
[4] Korea Adv Inst Sci & Technol, Dept Chem, Taejon 305701, South Korea
基金
新加坡国家研究基金会;
关键词
biosensor; graphene oxide; nanotechnology; peptide nucleic acid; RNA recognition; RT-PCR; QUANTIFICATION; EXPRESSION; DELIVERY; PROBES; PNA;
D O I
10.1021/nn401183s
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
MicroRNA (miRNA) is an important small RNA which regulates diverse gene expression at the post-transcriptional level. miRNAs are considered as important biomarkers since abnormal expression of specific miRNAs is associated with many diseases including cancer and diabetes. Therefore, it is important to develop biosensors to quantitatively detect miRNA expression levels. Here, we develop a nanosized graphene oxide (NGO) based miRNA sensor, which allows quantitative monitoring of target miRNA expression levels in living cells. The strategy is based on tight binding of NGO with peptide nucleic acid (PNA) probes, resulting in fluorescence quenching of the dye that is conjugated to the PNA, and subsequent recovery of the fluorescence upon addition of target miRNA. PNA as a probe for miRNA sensing offers many advantages including high sequence specificity, high loading capacity on the NGO surface compared to DNA and resistance against nuclease-mediated degradation. The present miRNA sensor allowed the detection of specific target miRNAs with the detection limit as low as similar to 1 pM and the simultaneous monitoring of three different miRNAs in a living cell.
引用
收藏
页码:5882 / 5891
页数:10
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