化学
生物分子
DNA
荧光
荧光显微镜
DNA纳米技术
滚动圆复制
DNA折纸
纳米技术
寡核苷酸
计算生物学
生物传感器
生物物理学
生物化学
DNA复制
生物
物理
量子力学
材料科学
作者
Liuchang Ma,Meng Shi,Yangyang Chang,Meng Liu
标识
DOI:10.1021/acs.analchem.1c01435
摘要
There is currently a great need for developing a simple and effective biosensing platform for the detection of single biomolecules (e.g., DNAs, RNAs, or proteins) in the biological, medical, and environmental fields. Here, we show a versatile and sensitive fluorescence counting strategy for quantifying proteins and microRNAs by employing functional DNA superstructures (denoted as 3D DNA). A 3D DNA biolabel was first engineered to become highly fluorescent and carry recognition elements for the target of interest. The presence of a target cross-links the resultant of the 3D DNA biolabel and a surface-bound capturing antibody or DNA oligonucleotide, thus forming a sandwich complex that can be easily resolved using traditional fluorescence microscopy. The broad utility of this platform is illustrated by engineering two different 3D DNA biolabels that enable the quantification of β-lactamase (one secreted bacterial hydrolase) and miR-21 (one overexpressed microRNA in cancer cells) with detection limits of 100 aM and 1 fM, respectively. We envision that the approach described herein will find useful applications in chemical biology, medical diagnostics, and biosensing.
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