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Nanoliter Quantitative High-Throughput Screening with Large-Scale Tunable Gradients Based on a Microfluidic Droplet Robot under Unilateral Dispersion Mode

机译:基于单侧分散模式下的微流体液滴机器人的大规模可调梯度,纳米射度量定量高通量筛选

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摘要

Performing quantitative high throughput screening (qHTS) is in urgent need in current chemical, biological, and medical research. In this work, we developed an automated microfluidic dilution and large-scale screening system in the nanoliter range, by combining the droplet-based microfluidic robot technique with a novel unilateral Taylor-Aril dispersion-based dilution approach. The unilateral dispersion approach utilizes multiphase microfluidic design to generate a concentration gradient with fast gradient generation time, low sample/reagent consumption, and high operation efficiency over the widely used bilateral Taylor-Aris dispersion approach adopted in previous dilution systems. The present system is capable of automatically generating a large and tunable range of concentration gradients covering ca. 6 orders of magnitude in droplet arrays and achieving qHTS of a large number of different samples. We applied the microfluidic droplet system in miniaturized enzyme kinetic assay in 8-nL droplets and high-throughput quantitative screening of enzyme inhibitors with a library of 102 compounds. Only 9.8 mu L of enzyme solution was consumed in 2448 droplet assays containing 102 compounds and 24 concentrations, representing an approximate 1600-fold reduction compared with multiwell plate-based assays. In the screening, dose-response curves of each tested compound were established and 4 hits (CP-471474, ilomastat, batimastat, and marimastat) were screened to have inhibitory activity to matrix metallopeptidase-9 (MMP-9), which demonstrated that the present system has the potential to provide a miniaturized qHTS platform for drug discovery.
机译:进行定量高通量筛选(QHT)迫切需要当前的化学,生物学和医学研究。在这项工作中,通过将基于液滴的微流体机器人技术与基于新的单侧泰勒 - 基础分散的稀释方法相结合,我们在纳米罐范围内开发了一种自动微流体稀释和大规模筛选系统。单侧分散方法利用多相微流体设计,产生具有快速梯度产生时间,低样品/试剂消耗的浓度梯度,以及在先前稀释系统中采用的广泛使用的双侧泰勒 - aris分散方法的高运行效率。本系统能够自动产生覆盖CA的大而可调范围的浓度梯度。液滴阵列中的6个数量级,并实现大量不同样本的QHT。我们在8-NL液滴中的小型化酶动力学测定中将微流体液滴系统应用于酶抑制剂的高通量定量筛选,具有102种化合物的文库。在含有102种化合物和24个浓度的2448滴测定中仅消耗仅9.8μL酶溶液,与基于多孔板的测定相比,表示近似1600倍的减少。在筛选中,建立了每种测试化合物的剂量 - 反应曲线,筛选4次次次次次次次次次次次次次次次次(CP-4714774,Ilomastat,BaTimastat和MariMastat,以对基质金属肽酶-9(MMP-9)具有抑制活性,这证明了目前的系统有可能为药物发现提供小型化的QHT平台。

著录项

  • 来源
    《Analytical chemistry》 |2019年第8期|共9页
  • 作者

    Wei Yan; Zhu Ying; Fang Qun;

  • 作者单位

    Zhejiang Univ Dept Chem Inst Microanalyt Syst Hangzhou 310058 Zhejiang Peoples R China;

    Zhejiang Univ Dept Chem Inst Microanalyt Syst Hangzhou 310058 Zhejiang Peoples R China;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 分析化学;
  • 关键词

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