高含量筛选
吞吐量
高分辨率
高通量筛选
光刻
材料科学
药品
显微镜
药物发现
纳米技术
计算机科学
化学
生物信息学
生物
医学
药理学
病理
生物化学
遥感
电信
无线
细胞
地质学
作者
Junfang Xie,Daobo Han,Shuai Xu,Haitong Zhang,Yonghe Li,Mingshan Zhang,Zhichao Deng,Jianguo Tian,Qing Ye
出处
期刊:ACS Nano
[American Chemical Society]
日期:2023-08-07
卷期号:17 (16): 15516-15528
被引量:3
标识
DOI:10.1021/acsnano.3c01865
摘要
A high-efficiency drug screening method is urgently needed due to the expanding number of potential targets and the extremely long time required to assess them. To date, high throughput and high content have not been successfully combined in image-based drug screening, which is the main obstacle to improve the efficiency. Here, we establish a high-throughput and high-content drug screening method by preparing a superhydrophobic microwell array plate (SMAP) and combining it with protein-retention expansion microscopy (proExM). Primarily, we described a flexible method to prepare the SMAP based on photolithography. Cells were cultured in the SMAP and treated with different drugs using a microcolumn–microwell sandwiching technology. After drug treatment, proExM was applied to realize super-resolution imaging. As a demonstration, a 7 × 7 image array of microtubules was successfully collected within 3 h with 68 nm resolution using this method. Qualitative and quantitative analyses of microtubule and mitochondria morphological changes after drug treatment suggested that more details were revealed after applying proExM, demonstrating the successful combination of high throughput and high content.
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