细胞内
单细胞分析
细胞
溶解
化学
生物物理学
基因
细胞生物学
计算生物学
多米诺骨牌
遗传学
生物
突变体
纳米技术
突变
材料科学
分子生物学
生物化学
催化作用
作者
Zaizai Dong,Shi Yan,Bing Liu,Yongcun Hao,Long Lin,Tianrui Chang,Hong Sun,Yusen Wang,Hu Li,Han Wu,Xinxin Hang,Shiqi He,Jiaming Hu,Xinying Xue,Nan Wu,Lingqian Chang
出处
期刊:Nano Letters
[American Chemical Society]
日期:2021-04-08
卷期号:21 (11): 4878-4886
被引量:28
标识
DOI:10.1021/acs.nanolett.1c00199
摘要
The genetic heterogeneities in cancer cells pose challenges to achieving precise drug treatment in a widely applicable manner. Most single-cell gene analysis methods rely on cell lysis for gene extraction and identification, showing limited capacity to provide the correlation of genetic properties and real-time cellular behaviors. Here, we report a single living cell analysis nanoplatform that enables interrogating gene properties and drug resistance in millions of single cells. We designed a Domino-probe to identify intracellular target RNAs while releasing 10-fold amplified fluorescence signals. An on-chip addressable microwell-nanopore array was developed for enhanced electro-delivery of the Domino-probe and in situ observation of cell behaviors. The proof-of-concept of the system was validated in primary lung cancer cell samples, revealing the positive-correlation of the ratio of EGFR mutant cells with their drug susceptibilities. This platform provides a high-throughput yet precise tool for exploring the relationship between intracellular genes and cell behaviors at the single-cell level.
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