Multiplex Digital MicroRNA Detection Using Cross-Inhibitory DNA Circuits.
Yannick RondelezGuillaume GinesPublished in: ACS sensors (2020)
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.
Keyphrases
- nucleic acid
- real time pcr
- single molecule
- label free
- loop mediated isothermal amplification
- transcription factor
- high throughput
- circulating tumor
- cell free
- atomic force microscopy
- gene expression
- living cells
- genome wide
- mass spectrometry
- gold nanoparticles
- dna methylation
- simultaneous determination
- oxidative stress
- liquid chromatography
- sensitive detection