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Multiplex Digital MicroRNA Detection Using Cross-Inhibitory DNA Circuits
Author(s) -
Yannick Rondelez,
Guillaume Gines
Publication year - 2020
Publication title -
acs sensors
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 2.055
H-Index - 57
ISSN - 2379-3694
DOI - 10.1021/acssensors.0c00593
Subject(s) - multiplex , loop mediated isothermal amplification , computational biology , microrna , dna , digital polymerase chain reaction , multiplex polymerase chain reaction , transcription (linguistics) , reverse transcriptase , biology , rna , chemistry , microbiology and biotechnology , polymerase chain reaction , gene , genetics , linguistics , philosophy
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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