2011
DOI: 10.1039/c0cc04350h
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A reagentless and disposable electronic genosensor: from multiplexed analysis to molecular logic gates

Abstract: Reagentless, sensitive and multiplexed analysis of gyrB and K-ras gene biomarkers is achieved based on the proximity changes of two different redox-tags to the electrode surface upon DNA hybridizations, and the presence of the two gene biomarkers also acts as inputs and activates the logic gate.

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Cited by 47 publications
(25 citation statements)
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“…334 DNA sensors based on hairpin structures equipped with redox-tags and immobilized on electrode surfaces have also been reported. 335,336 Another approach to design DNA-based logic gates is to use DNA molecules with biocatalytic properties mimicking enzyme functions, so-called DNAzymes. 337 Willner et al have designed an entire DNA computing circuit based on the modular coupling of DNAzyme subunits.…”
Section: Information Storage and Processingmentioning
confidence: 99%
“…334 DNA sensors based on hairpin structures equipped with redox-tags and immobilized on electrode surfaces have also been reported. 335,336 Another approach to design DNA-based logic gates is to use DNA molecules with biocatalytic properties mimicking enzyme functions, so-called DNAzymes. 337 Willner et al have designed an entire DNA computing circuit based on the modular coupling of DNAzyme subunits.…”
Section: Information Storage and Processingmentioning
confidence: 99%
“…electrode surface. Despite this and other recent advances, sensors that employ only one signaling mechanism can still be limiting [78,82,83]. For this reason, it is noteworthy that the use of multiple redox labels (e.g., Fc and MB), as developed by Lai et al [84], is capable of providing additional electrochemical information at various redox potentials ( Fig.…”
Section: Samsmentioning
confidence: 99%
“…They have been widely applied in the detection of meaningful analytes, such as thrombin [8][9][10][11], cocaine [12][13][14][15][16], adenosine triphosphate [10,17,18], lysozyme [19,20], and platelet-derived growth factor [21,22]. Many of the E-AB biosensors are based on the single signaling response [9,13,18,23], while some papers focus on the dual-signaling E-AB sensors due to the advantages of high sensitivity and low detection limit [24][25][26][27].…”
Section: Introductionmentioning
confidence: 99%
“…Usually, the construction of dual-signaling E-AB sensors is based on two partially or completely complementary DNA chains, each of which is tagged with redox species at one end of the chain, and the targets chosen for detection typically have only one aptamer-binding site [24][25][26]. However, many targets, such as thrombin [28,29], platelet-derived growth factor [30,31], prostate specific antigen [32], and vascular endothelial growth factors [33] and MUC1 protein [34], have more than one sites to bind their aptamers or antibodies to form a sandwich structure, which has an obviously better anti-interference ability than the simple biosensing structure [35].…”
Section: Introductionmentioning
confidence: 99%