2017
DOI: 10.1016/j.snb.2017.01.017
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Label-free, non-enzymatic and ultrasensitive electrochemical nucleic acid biosensing by tandem DNA-fueled target recycling and hybridization chain reaction

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Cited by 13 publications
(6 citation statements)
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“…Inspired by these biological examples, the initial impetus for devising enzyme-free DNA reaction networks displaying catalytic behavior was to make artificial systems that behave like free-running motors rather then the stepped DNA motors briefly discussed above . Since catalytic systems can function as chemical amplifiers, the application of enzyme free DNA-based catalytic networks as sensor and detector systems later became a major driving force in the development of these systems. , …”
Section: Catalytic Processes Based On Strand Displacementmentioning
confidence: 99%
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“…Inspired by these biological examples, the initial impetus for devising enzyme-free DNA reaction networks displaying catalytic behavior was to make artificial systems that behave like free-running motors rather then the stepped DNA motors briefly discussed above . Since catalytic systems can function as chemical amplifiers, the application of enzyme free DNA-based catalytic networks as sensor and detector systems later became a major driving force in the development of these systems. , …”
Section: Catalytic Processes Based On Strand Displacementmentioning
confidence: 99%
“…This involves toehold-mediated strand displacement combined with molecular beacons, dendritic assemblies from DNA and PNA, and various sensors based on fluorogenic G quadruplexes. , Strand displacement schemes were combined with surface enhanced Raman scattering (SERS), electrochemiluminescence, or enzymatic amplification by acetylcholinesterase, to name but a few. Depending on the specific scheme and the number of amplification steps, limits of detection in the picomolar, femtomolar, ,,, or even attomolar range ,, were reported.…”
Section: Applications In Sensing Diagnostics and Therapeuticsmentioning
confidence: 99%
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“…Analogously, an improved in-situ DNA HCR named quick HCR-FISH was tested for the rapid and sensitive identification of marine bacteria with low rRNA contents not only in seawater but also in sediment samples [ 136 ]. Recently, HCR acting in tandem with a DNA-fueled target recycling reaction was used for the isothermal, label-free, non-enzymatic amplification and ultra-sensitive electrochemical detection of nucleic acids [ 137 ]. Although it was only a proof-of-concept (depicted in Figure 5 ), the tandem could be exploited in environmental analysis of pathogens from aquatic ecosystems.…”
Section: Enhancing Performancementioning
confidence: 99%