A Rapid, Amplification-Free, and Sensitive Diagnostic Assay for Single-Step Multiplexed Fluorescence Detection of MicroRNA

被引:161
作者
Jin, Zongwen [1 ,2 ]
Geissler, Daniel [3 ]
Qiu, Xue [1 ,2 ]
Wegner, K. David [1 ,2 ]
Hildebrandt, Niko [1 ,2 ]
机构
[1] Univ Paris 11, NanoBioPhoton Nanofret Com, Inst Elect Fondamentale, F-91405 Orsay, France
[2] CNRS, F-91405 Orsay, France
[3] Fed Inst Mat Res & Testing, BAM, Div Biophoton 1 10, Berlin, Germany
关键词
clinical diagnostics; FRET; microRNA; multiplexing; time-gated fluorescence detection; RESONANCE ENERGY-TRANSFER; CANCER; QUANTIFICATION; BIOSENSOR; LIGATION;
D O I
10.1002/anie.201504887
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The importance of microRNA (miRNA) dysregulation for the development and progression of diseases and the discovery of stable miRNAs in peripheral blood have made these short-sequence nucleic acids next-generation biomarkers. Here we present a fully homogeneous multiplexed miRNA FRET assay that combines careful biophotonic design with various RNA hybridization and ligation steps. The single-step, single-temperature, and amplification-free assay provides a unique combination of performance parameters compared to state-of-the-art miRNA detection technologies. Precise multiplexed quantification of miRNA-20a, -20b, and -21 at concentrations between 0.05 and 0.5 nm in a single 150 mu L sample and detection limits between 0.2 and 0.9 nm in 7.5 mu L serum samples demonstrate the feasibility of both high-throughput and point-of-care clinical diagnostics.
引用
收藏
页码:10024 / 10029
页数:6
相关论文
共 31 条
[1]   Diversifying microRNA sequence and function [J].
Ameres, Stefan L. ;
Zamore, Phillip D. .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2013, 14 (08) :475-488
[2]   Target RNA-Directed Trimming and Tailing of Small Silencing RNAs [J].
Ameres, Stefan L. ;
Horwich, Michael D. ;
Hung, Jui-Hung ;
Xu, Jia ;
Ghildiyal, Megha ;
Weng, Zhiping ;
Zamore, Phillip D. .
SCIENCE, 2010, 328 (5985) :1534-1539
[3]   In vitro quantification of specific microRNA using molecular beacons [J].
Baker, Meredith B. ;
Bao, Gang ;
Searles, Charles D. .
NUCLEIC ACIDS RESEARCH, 2012, 40 (02) :e13
[4]   MicroRNAs: Target Recognition and Regulatory Functions [J].
Bartel, David P. .
CELL, 2009, 136 (02) :215-233
[5]   Highly Sensitive Determination of microRNA Using Target-Primed and Branched Rolling-Circle Amplification [J].
Cheng, Yongqiang ;
Zhang, Xian ;
Li, Zhengping ;
Jiao, Xiaoxia ;
Wang, Yucong ;
Zhang, Yali .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2009, 48 (18) :3268-3272
[6]   Bioluminescence-based detection of MicroRNA, miR21 in breast cancer cells [J].
Cissell, Kyle A. ;
Rahimi, Yasmeen ;
Shrestha, Suresh ;
Hunt, Eric A. ;
Deo, Sapna K. .
ANALYTICAL CHEMISTRY, 2008, 80 (07) :2319-2325
[7]   Detection methods for microRNAs in clinic practice [J].
de Planell-Saguer, Mariangels ;
Celina Rodicio, Maria .
CLINICAL BIOCHEMISTRY, 2013, 46 (10-11) :869-878
[8]   Analytical aspects of microRNA in diagnostics: A review [J].
de Planell-Saguer, Mariangels ;
Celina Rodicio, Maria .
ANALYTICA CHIMICA ACTA, 2011, 699 (02) :134-152
[9]   A simple rapid detection method of DNA based on ligation-mediated real-time fluorescence PCR [J].
Du, Yu Qing ;
Gao, Peng Fei ;
Wang, Wei ;
Wang, Ting Ting ;
Chang, Yong ;
Wang, Jian ;
Huang, Cheng Zhi .
ANALYST, 2013, 138 (19) :5745-5750
[10]  
Frampton AE, 2013, EXPERT REV MOL DIAGN, V13, P31, DOI [10.1586/ERM.12.136, 10.1586/erm.12.136]