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

被引:158
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
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