Enzymatic Litmus Test for Selective Colorimetric Detection of C-C Single Nucleotide Polymorphisms

被引:29
|
作者
Wolfe, Michael G. [1 ]
Ali, M. Monsur [1 ]
Brennan, John D. [1 ]
机构
[1] McMaster Univ, Biointerfaces Inst, 1280 Main St West, Hamilton, ON L8S 4O3, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
JACK BEAN UREASE; METAL-IONS; PAPER SENSORS; POINT; INHIBITION; BIOSENSOR; BINDING; DNA; AG; HG;
D O I
10.1021/acs.analchem.9b00235
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
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 detection of 11 nM DNA in 40 min. The assay system is easy to use, portable, and stable for at least 30 days at ambient temperature. To assess the versatility and practical application of the paper sensor, we used it to identify a G > C transversion present in human genomic DNA from a ductal carcinoma cell line, a mutation commonly found in breast cancer. We believe this new assay system has the potential to be a low-cost method for rapidly identifying DNA with the C-C mismatch SNP as a means of cancer screening in resource-limited areas.
引用
收藏
页码:4735 / 4740
页数:6
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