Multiplex Digital MicroRNA Detection Using Cross-Inhibitory DNA Circuits

被引:20
|
作者
Rondelez, Yannick [1 ]
Gines, Guillaume [1 ]
机构
[1] Univ PSL, Gulliver Lab, ESPCI Paris, F-75005 Paris, France
来源
ACS SENSORS | 2020年 / 5卷 / 08期
基金
欧洲研究理事会;
关键词
multiplex assay; DNA circuit; microRNA; digital droplet detection; isothermal amplification; STRAND DISPLACEMENT AMPLIFICATION; ROLLING CIRCLE AMPLIFICATION; NUCLEIC-ACID AMPLIFICATION; QUANTIFICATION; POLYMERASE; CHEMISTRY; PLATFORM; MIRNA;
D O I
10.1021/acssensors.0c00593
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Ubiquitous post-transcriptional regulators in eukaryotes, microRNAs are currently emerging as promising biomarkers of physiological and pathological processes. Multiplex and digital detection of microRNAs represents a major challenge toward the use of microRNA signatures in clinical settings. The classical reverse transcription polymerase chain reaction quantification approach has important limitations because of the need for thermocycling and a reverse transcription step. Simpler, isothermal alternatives have been proposed, yet none could be adapted in both a digital and multiplex format. This is either because of a lack of sensitivity that forbids single molecule detection or molecular cross-talk reactions that are responsible for nonspecific amplification. Building on an ultrasensitive isothermal amplification mechanism, we present a strategy to suppress cross-talk reactions, allowing for robust isothermal and multiplex detection of microRNA targets. Our approach relies on target-specific DNA circuits interconnected with DNA-encoded inhibitors that repress nonspecific signal amplification. We demonstrate the one-step, isothermal, digital, and simultaneous quantification of various pairs of important microRNA targets.
引用
收藏
页码:2430 / 2437
页数:8
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