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在微笼阵列芯片中形成大规模液滴阵列用于高通量筛选。

Forming a Large-Scale Droplet Array in a Microcage Array Chip for High-Throughput Screening.

机构信息

Institute of Analytical Chemistry, Department of Chemistry and Center for Chemistry of Novel & High-Performance Materials , Zhejiang University , Hangzhou , 310058 , China.

出版信息

Anal Chem. 2019 Aug 20;91(16):10757-10763. doi: 10.1021/acs.analchem.9b02288. Epub 2019 Aug 6.

Abstract

Forming a large-scale droplet array plays an important role for microfluidic droplet-based high-throughput screening and analysis. Herein, we describe a simple and rapid method to form a large-scale two-dimension (2D) droplet array by using a microcage array chip. Differing from the previous droplet array formation methods, microcages formed by being surrounded by multiple micropillars could rapidly spread the oil phase through the gaps between the micropillars and trap droplets with fast speed and convenient operation. We formed a large-scale 2D monolayer droplet array containing approximately 1 000 000 droplets on a 5.5 cm × 5.5 cm microcage array chip within 90 s. The droplets in the droplet array could be further incubated for performing biochemical reactions and detected by a fluorescence microscope in real time. Due to the exact trapping and positioning functions of the microcages to the droplets, single targeted fluorescent droplets in the array could be individually picked out and transferred to culture medium by a microfluidic droplet-handling robot with a success rate of 100% and a picking operation time of 2.0 s for one droplet under the optimized conditions. This system was validated in the screening of the bacterium expressing the esterase AFEST from a mixture of AFEST-expressing and phosphotriesterase-expressing cells, achieving a success rate of 100% for single-droplet picking while maintaining the bacterial cell viability. The present system has the potential to be applied in high-throughput screening and analysis, such as single cell analysis, directed evolution, and drug screening.

摘要

形成大规模液滴阵列对于微流控液滴为基础的高通量筛选和分析起着重要作用。在此,我们描述了一种通过微笼阵列芯片形成大规模二维(2D)液滴阵列的简单快速的方法。与之前的液滴阵列形成方法不同,由多个微柱包围形成的微笼可以通过微柱之间的间隙快速扩散油相,并以快速的速度和方便的操作捕获液滴。我们在 90 秒内于 5.5cm×5.5cm 的微笼阵列芯片上形成了一个含有约 100 万个液滴的大规模 2D 单层液滴阵列。在液滴阵列中的液滴可以进一步孵育,用于进行生化反应,并通过荧光显微镜实时检测。由于微笼对液滴具有精确的捕获和定位功能,在优化条件下,阵列中的单个靶向荧光液滴可以被微流控液滴处理机器人以 100%的成功率和 2.0 秒的单个液滴操作时间单独挑出并转移到培养基中。该系统在筛选混合表达 AFEST 的菌和表达磷酸三酯酶的菌中表达的酯酶 AFEST 的混合物中得到了验证,对于单个液滴的挑取成功率为 100%,同时保持了细菌细胞的活力。该系统具有在高通量筛选和分析中应用的潜力,如单细胞分析、定向进化和药物筛选。

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