2019
DOI: 10.1039/c8sc05217d
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Programmable intracellular DNA biocomputing circuits for reliable cell recognitions

Abstract: A reconfigurable hybridization-based chain reaction was introduced to assemble enzyme-free DNA logic gates and advanced logic circuits for analyzing multiple endogenous miRNA expressions and discriminating different living cells.

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Cited by 87 publications
(76 citation statements)
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“…, MCF-7 breast cancer cells, HepG2 liver cancer cells), in comparison to normal epithelial breast cells MCF-10A. The MCF-7 cells include the miRNA-21 and miRNA-155 as biomarkers, 57 and the HepG2 cells overexpress miRNA-21. 58 Accordingly, the different cells were treated with the tetrahedra composite shown in Scheme 1 that includes three quenched fluorophores, FAM, Cy5, and ROX.…”
Section: Resultsmentioning
confidence: 99%
“…, MCF-7 breast cancer cells, HepG2 liver cancer cells), in comparison to normal epithelial breast cells MCF-10A. The MCF-7 cells include the miRNA-21 and miRNA-155 as biomarkers, 57 and the HepG2 cells overexpress miRNA-21. 58 Accordingly, the different cells were treated with the tetrahedra composite shown in Scheme 1 that includes three quenched fluorophores, FAM, Cy5, and ROX.…”
Section: Resultsmentioning
confidence: 99%
“…Placing DNA gates on a tile allows for a modular approach to circuit assembling, in which logic units can be produced separately and stored for extended time before being integrated in more complex circuits [5] . In this paradigm, each NAND gate can be chemically crosslinked to minimize the risk of strand separation and mishybridization in complex mixtures of DNA strands during assembling complex circuits.…”
Section: Resultsmentioning
confidence: 99%
“…Moreover, the biocompatibility of such devices would enable analysis of complex sets of biomarkers, including those found in individual cells. This promises to advance diagnostics and the treatment of infectious diseases, genetic disorders, and cancers [4–7] …”
Section: Introductionmentioning
confidence: 99%
“…More recently, DNA motif and miRNA‐based biocomputing circuits for various cell recognition activities using fluorescence intensity were reported. [ 117 ] This research defined the biocomputation as the two modules of DNA as the sensing module and processing module that structure performed by hybridization chain reaction (HCR) that amplified the hybridization events of target with fluorescence (fluorescein amidite [FAM]‐tagged module) (Figure 4B). Other modules tagged with TAMRA quench the counterpart of the biocomputation module for signal amplification and are processed by Forster resonance energy transfer (FRET).…”
Section: Bioelectronic Devices Comprised Of Nucleic Acid Based Nanobimentioning
confidence: 99%