2017
DOI: 10.1007/s00604-017-2272-6
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Fluorescence based turn-on strategy for determination of microRNA-155 using DNA-templated copper nanoclusters

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Cited by 71 publications
(23 citation statements)
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“…In Cu‐NPs design, one of the challenges is how to regulate the emission of fluorescence of various wavelengths for multiplex analysis. Therefore, oligonucleotide‐templated Cu‐NPs was developed as a method which utilized for measurement of the fluorescence shift that occurs after DNA‐RNA heteroduplex formation . The oligonucleotide probe acts as a template for Cu‐NPs synthesis, which shows strong fluorescence enhancement at 490 nm while the subsequent formation of DNA‐RNA heteroduplex when the probe binds target miRNA (miRNA‐155) cause a 90 nm Stokes shift.…”
Section: The Application Of Dna‐templated Cu‐nps Sensing Of Various Tmentioning
confidence: 99%
See 1 more Smart Citation
“…In Cu‐NPs design, one of the challenges is how to regulate the emission of fluorescence of various wavelengths for multiplex analysis. Therefore, oligonucleotide‐templated Cu‐NPs was developed as a method which utilized for measurement of the fluorescence shift that occurs after DNA‐RNA heteroduplex formation . The oligonucleotide probe acts as a template for Cu‐NPs synthesis, which shows strong fluorescence enhancement at 490 nm while the subsequent formation of DNA‐RNA heteroduplex when the probe binds target miRNA (miRNA‐155) cause a 90 nm Stokes shift.…”
Section: The Application Of Dna‐templated Cu‐nps Sensing Of Various Tmentioning
confidence: 99%
“…Therefore, oligonucleotide-templated Cu-NPs was developed as a method which utilized for measurement of the fluorescence shift that occurs after DNA-RNA heteroduplex formation. [79] The oligonucleotide probe acts as a template for Cu-NPs synthesis, which shows strong fluorescence enhancement at 490 nm while the subsequent formation of DNA-RNA heteroduplex when the probe binds target miRNA (miRNA-155) cause a 90 nm Stokes shift. This method could quantify target RNA over a linear range of 50 pM to 10 nM, while a detection limit of 11 pM was realized.…”
Section: Other Biological Sensing Conceptsmentioning
confidence: 99%
“…Conjugation of peroxidase mimic nanostructure with bio‐receptor not only decreased catalytic activity but also diminish binding affinity of bio‐receptor . Nowadays DNA has been attractive for its potency as a scaffold for synthesis of nanoclusters . This capacity resolved bio receptor conjugation in designing DNA biosensor.…”
Section: Introductionmentioning
confidence: 99%
“…[33] Nowadays DNA has been attractive for its potency as a scaffold for synthesis of nanoclusters. [34][35][36][37][38][39] This capacity resolved bio receptor conjugation in designing DNA biosensor. As of yet DNA-Ag/Pt nanoclusters have been used for fabrication of biosensors for L-Cysteine [40] and thrombin colorimetric assay.…”
Section: Introductionmentioning
confidence: 99%
“…Further, this work demonstrated the linear range from 1 pM to 10 nM with an LOD of 1 pM. By contrast, Prof. Hosseini described the DNA-Cu NC-based "turn-on" recognition of microRNA-155 [152]. In which, DNA-Cu NCs witnessed linear fluorescent enhancement towards miRNA-155 between 50 pM to 10 nM, with an LOD value of 11 pM.…”
Section: Sensor Applications Of Cu Ncsmentioning
confidence: 99%