Key Laboratory of Weak-Light Nonlinear Photonics, Ministry of Education, School of Physics and TEDA Applied Physics, Nankai University, Tianjin 300071, China.
Institute of Modern Optics, Nankai University, Tianjin 300350, China.
ACS Nano. 2023 Aug 22;17(16):15516-15528. doi: 10.1021/acsnano.3c01865. Epub 2023 Aug 7.
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.
由于潜在靶点数量不断增加,以及评估这些靶点所需的时间极其漫长,因此迫切需要一种高效的药物筛选方法。迄今为止,基于图像的药物筛选尚未成功地将高通量和高内涵结合在一起,这是提高效率的主要障碍。在这里,我们通过制备超疏水微井阵列板(SMAP)并将其与蛋白保留扩展显微镜(proExM)相结合,建立了一种高通量和高内涵的药物筛选方法。首先,我们描述了一种基于光刻法制备 SMAP 的灵活方法。将细胞培养在 SMAP 中,并使用微柱-微井夹层技术用不同的药物处理。药物处理后,应用 proExM 实现超分辨率成像。作为演示,使用该方法在 3 小时内成功收集了 7×7 个微管图像阵列,分辨率为 68nm。对药物处理后微管和线粒体形态变化的定性和定量分析表明,应用 proExM 后揭示了更多细节,成功地将高通量和高内涵结合在一起。