Spatially Resolved, Error-Robust Multiplexed MicroRNA Profiling in Single Living Cells

被引:6
|
作者
Wei, Wei [1 ]
Dai, Wenhao [1 ]
Yang, Fan [1 ]
Lu, Huiting [3 ]
Zhang, Kai [4 ]
Xing, Yi [1 ]
Meng, Xiangdan [1 ]
Zhou, Liping [1 ]
Zhang, Yiyi [1 ]
Yang, Qiqi [1 ]
Cheng, Yaru [1 ]
Dong, Haifeng [1 ,2 ]
机构
[1] Univ Sci & Technol Beijing, Sch Chem & Biol Engn, Beijing Key Lab Bioengn & Sensing Technol, 30 Xueyuan Rd, Beijing 100083, Peoples R China
[2] Shenzhen Univ, Hlth Sci Ctr, Sch Biomed Engn, Marshall Lab Biomed Engn,Res Ctr Biosensor & Nano, 3688 Nanhai Rd, Shenzhen 518060, Guangdong, Peoples R China
[3] Univ Sci & Technol Beijing, Sch Chem & Biol Engn, Dept Chem, 30 Xueyuan Rd, Beijing 100083, Peoples R China
[4] Beijing Univ Chem Technol, Coll Mat Sci & Engn, Beijing 100029, Peoples R China
基金
国家自然科学基金重大项目; 中国国家自然科学基金;
关键词
Error Correction; Living Cell Imaging; MicroRNA Multiplexed Detection; Nanoparticles; Spatial Resolution; AMPLIFICATION; BARCODES;
D O I
10.1002/anie.202116909
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Simultaneous imaging of multiple microRNAs (miRNAs) in individual living cells is challenging due to the lack of spectrally distinct encoded fluorophores and non-cytotoxic methods. We describe a multiplexed error-robust combinatorial fluorescent label-encoding method, termed fluorophores encoded error-corrected labels (FluoELs), enabling multiplexed miRNA imaging in living cells with error-correcting capability. The FluoELs comprise proportional dual fluorophores for encoding and a constant quantitative single fluorophore for error-corrected quantification. Both are embedded in 260 nm core-shell silica nanoparticles modified with molecular beacon detection probes. The FluoELs are low cytotoxic and could accurately quantify and spatially resolve nine breast-cancer-related miRNAs and evaluate their coordination. The FluoELs enabled a single-cell analysis platform to evaluate miRNA expression profiles and the molecular mechanisms underlying miRNA-associated diseases.
引用
收藏
页数:9
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