适体
多路复用
荧光团
荧光
配体(生物化学)
DNA
分析物
化学
DNA折纸
核酸内切酶
生物物理学
材料科学
组合化学
生物
分子生物学
生物信息学
生物化学
物理
受体
物理化学
量子力学
作者
Zhixin Zhou,Yang Sung Sohn,Rachel Nechushtai,Itamar Willner
出处
期刊:ACS Nano
[American Chemical Society]
日期:2020-06-15
卷期号:14 (7): 9021-9031
被引量:127
标识
DOI:10.1021/acsnano.0c04031
摘要
The sensing modules for analyzing miRNAs or the endonucleases consist of tetrahedra functionalized with three different fluorophore-quencher pairs in spatially quenched configurations and hairpin units acting as recognition elements for the analytes. Three different miRNAs (miRNA-21, miRNA-221, and miRNA-155) or three different endonucleases (Nt.BbvCI, EcoRI, and HindIII) uncage the respective hairpins, leading to the switched-on fluorescence of the respective fluorophores and to the multiplex detection of the respective analytes. In addition, a tetrahedron module for the multiplexed analysis of aptamer ligand complexes (ligands = ATP, thrombin, VEGF) is introduced. The module includes edges modified with three spatially separated fluorophore-quencher pairs that were stretched by the respective aptamer strands to yield a switched-on fluorescent state. Formation of the respective aptamer ligands reconfigures the edges into fluorophore-quenched caged-hairpin structures that enable the multiplexed analysis of the aptamer-ligand complexes. The facile permeation of the tetrahedra structures into cells is used for the imaging of MCF-7 and HepG2 cancer cells and their discrimination from normal epithelial MCF-10A breast cells.
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