Highly Sensitive RNA-Cleaving DNAzyme Sensors from Surface-to-Surface Product Enrichment

被引:11
作者
Samani, Sahar Esmaeili [2 ]
Chang, Dingran [1 ]
McConnell, Erin M. [1 ]
Rothenbroker, Meghan [1 ]
Filipe, Carlos D. M. [2 ]
Li, Yingfu [1 ]
机构
[1] McMaster Univ, Dept Biochem & Biomed Sci, 1280 Main St West, Hamilton, ON L8S 4K1, Canada
[2] McMaster Univ, Dept Chem Engn, 1280 Main St West, Hamilton, ON L8S 4K1, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
bacterial pathogens; biosensors; DNAzymes; paper sensors; RNA; RNA cleavage; IN-VITRO SELECTION; DNA; AMPLIFICATION; ENZYMES;
D O I
10.1002/cbic.201900575
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The engineering of easy-to-use biosensors with ultra-low detection sensitivity remains a major challenge. Herein, we report a simple approach for creating such sensors through the use of an RNA-cleaving DNAzyme (RcD) and a strategy designed to concentrate its cleavage product significantly. The assay uses micron-sized beads loaded with a target-responsive RcD and a paper strip containing a microzone covered with a DNA oligonucleotide capable of capturing the cleavage product of the RcD through Watson-Crick hybridization. Placing the beads and the paper strip in a target-containing test sample allows the bead-bound RcD molecules to undergo target-induced RNA cleavage, releasing a DNA fragment that is captured by the paper strip. This strategy, though simple, is very effective in achieving high levels of detection sensitivity, being able to enrich the concentration of the cleavage product by three orders of magnitude. It is also compatible with both fluorescence-based and colorimetric reporting mechanisms. This work provides a simple platform for developing ultrasensitive biosensors that take advantage of the widely available RcDs as molecular recognition elements.
引用
收藏
页码:632 / 637
页数:6
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