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:116
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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