Isothermal digital detection of microRNAs using background-free molecular circuit

被引:81
作者
Gines, Guillaume [1 ]
Menezes, Roberta [2 ]
Nara, Kaori [1 ]
Kirstetter, Anne-Sophie [1 ]
Taly, Valerie [2 ]
Rondelez, Yannick [1 ]
机构
[1] PSL Res Univ, ESPCI Paris, CNRS, Lab Gulliver, 10 Rue Vauquelin, F-75005 Paris, France
[2] Univ Paris 05, Univ Paris Diderot, Equipe Labellisee Ligue Natl Canc, Ctr Rech Cordeliers,INSERM,CNRS,Sorbonne Univ,USP, Paris, France
基金
欧洲研究理事会;
关键词
CIRCULATING MICRORNA; QUANTITATIVE PCR; AMPLIFICATION; QUANTIFICATION; POLYMERASE; DIAGNOSIS;
D O I
10.1126/sciadv.aay5952
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
MicroRNAs, a class of transcripts involved in the regulation of gene expression, are emerging as promising disease-specific biomarkers accessible from tissues or bodily fluids. However, their accurate quantification from biological samples remains challenging. We report a sensitive and quantitative microRNA detection method using an isothermal amplification chemistry adapted to a droplet digital readout. Building on molecular programming concepts, we design a DNA circuit that converts, thresholds, amplifies, and reports the presence of a specific microRNA, down to the femtomolar concentration. Using a leak absorption mechanism, we were able to suppress nonspecific amplification, classically encountered in other exponential amplification reactions. As a result, we demonstrate that this isothermal amplification scheme is adapted to digital counting of microRNAs: By partitioning the reaction mixture into water-in-oil droplets, resulting in single microRNA encapsulation and amplification, the method provides absolute target quantification. The modularity of our approach enables to repurpose the assay for various microRNA sequences.
引用
收藏
页数:8
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