2019
DOI: 10.1021/acs.analchem.9b00235
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Enzymatic Litmus Test for Selective Colorimetric Detection of C–C Single Nucleotide Polymorphisms

Abstract: A paper based litmus test has been developed using modulation of urease enzyme activity for detection of C–C mismatch single nucleotide polymorphisms (SNPs) by the naked eye. Urease is first inactivated with silver ions and printed onto paper microzones. Addition of DNA containing C–C mismatches reactivates urease via binding of Ag­(I), allowing restoration of urease activity, hydrolysis of urea to produce ammonia, and an increase in pH, which is monitored colorimetrically using a pH indicator with a limit of … Show more

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Cited by 31 publications
(29 citation statements)
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“…Wearable devices are becoming increasingly popular for maximizing the benefits of healthy living. [1][2][3][4] Colorimetric biosensors are particularly advantageous for this purpose because they can leverage the camera of a smartphone for signal detection. This allows for a streamlined design that simplifies the fabrication of the wearable device and ensures an easy integration with health apps.…”
Section: Introductionmentioning
confidence: 99%
“…Wearable devices are becoming increasingly popular for maximizing the benefits of healthy living. [1][2][3][4] Colorimetric biosensors are particularly advantageous for this purpose because they can leverage the camera of a smartphone for signal detection. This allows for a streamlined design that simplifies the fabrication of the wearable device and ensures an easy integration with health apps.…”
Section: Introductionmentioning
confidence: 99%
“…To avoid the influence of assay buffer on the pH value of the sensing solution, a slightly acidic substrate solution (pH 5.8) which only contains phenol red and urea was used to initiate the color change. And the pH of the assay solution is in the optimal pH range for urease catalysis [27]. The principle of the colorimetric sensor is illustrated in Scheme 1.…”
Section: Resultsmentioning
confidence: 99%
“…This indicates that enough pcDNA and probe DNA had been hybridized at this time, and the reaction was complete. In addition, based on the results of detection of SNPs reported in previous studies (Supplementary Table S2; Wei et al, 2016;Xu et al, 2018;Wolfe et al, 2019), this paper uses graphene oxide-based SYBR Green I fluorescent intercalating dye-induced sensors to detect SNPs with a low detection limit (1 nM). The response time is faster (15 s).…”
Section: The Sensitivity Of the Biosensormentioning
confidence: 99%