Direct Electrocatalytic mRNA Detection Using PNA-Nanowire Sensors

被引:66
作者
Fang, Zhichao
Kelley, Shana O. [1 ]
机构
[1] Univ Toronto, Dept Pharmaceut Sci, Leslie Dan Fac Pharm, Toronto, ON M5S 3M2, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
DNA HYBRIDIZATION; ELECTRICAL DETECTION; PROSTATE-CANCER; LABEL-FREE; BIOSENSORS; SEQUENCES; ELECTRODE; AMPLIFICATION; SPECTROSCOPY; MICROARRAYS;
D O I
10.1021/ac801890f
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
We report an electrochemical nucleic acids sensing system that exhibits high sensitivity and specificity when challenged with heterogeneous samples of RNA. The platform directly detects specific RNA sequences in cellular and clinical samples without any sample labeling or PCR amplification. The sensor features an electrode platform consisting of three-dimensional gold nanowires, and DNA or RNA hybridization is detected using an electrocatalytic reporter system. In this study, probes made of peptide nucleic acid (PNA) are used to detect a newly identified cancer biomarker-a gene fusion recently associated with prostate cancer. The system is able to detect the fusion sequence with 100 fM sensitivity, and retains high sensitivity even in the presence of a large excess of non-complementary sequences. Moreover, the sensor is able to detect the fusion sequence in as little as 10 ng of mRNA isolated from cell lines or 100 ng total RNA from patient tissue samples. The PNA-nanowire nucleic acids sensor described is one of the first electrochemical sensors to directly detect specific mRNAs in unamplified patient samples.
引用
收藏
页码:612 / 617
页数:6
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