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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.
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收藏
页码:2430 / 2437
页数:8
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