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Droplet microfluidics with magnetic beads: a new tool to investigate drug–protein interactions

机译:带有磁珠的液滴微流控:研究药物-蛋白质相互作用的新工具

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摘要

In this study, we give the proof of concept for a method to determine binding constants of compounds in solution. By implementing a technique based on magnetic beads with a microfluidic device for segmented flow generation, we demonstrate, for individual droplets, fast, robust and complete separation of the magnetic beads. The beads are used as a carrier for one binding partner and hence, any bound molecule is separated likewise, while the segmentation into small microdroplets ensures fast mixing, and opens future prospects for droplet-wise analysis of drug candidate libraries. We employ the method for characterization of drug–protein binding, here warfarin to human serum albumin. The approach lays the basis for a microfluidic droplet-based screening device aimed at investigating the interactions of drugs with specific targets including enzymes and cells. Furthermore, the continuous method could be employed for various applications, such as binding assays, kinetic studies, and single cell analysis, in which rapid removal of a reactive component is required.
机译:在这项研究中,我们给出了确定溶液中化合物结合常数的方法的概念证明。通过使用基于磁珠的微流体装置实现分段流生成的技术,我们证明了对于单个液滴,磁珠的快速,坚固和完全分离。珠子用作一个结合伴侣的载体,因此,任何结合的分子也同样被分离,而切成小微滴的片段可确保快速混合,并为药物候选库的逐滴分析开辟了未来的前景。我们采用表征药物-蛋白质结合的方法,此处为华法林与人血清白蛋白的结合。该方法为旨在研究药物与特定靶标(包括酶和细胞)的相互作用的基于微流体液滴的筛选设备奠定了基础。此外,连续方法可用于各种应用,例如结合测定,动力学研究和单细胞分析,其中需要快速去除反应性组分。

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