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Interfacing Microwells with Nanoliter Compartments: A Sampler Generating High-Resolution Concentration Gradients for Quantitative Biochemical Analyses in Droplets

机译:微孔与纳升隔室的接口:生成高浓度梯度的液滴的定量生化分析的采样器

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Analysis of concentration dependencies is key to the quantitative understanding of biological and chemical systems. In experimental tests involving concentration gradients such as inhibitor library screening, the number of data points and the ratio between the stock volume and the volume required in each test determine the quality and efficiency of the information gained. Titerplate assays are currently the most widely used format, even though they require microlitre volumes. Compartmentalization of reactions in pico- to nanoliter water-in-oil droplets in microfluidic devices provides a solution for massive volume reduction. This work addresses the challenge of producing microfluidic-based concentration gradients in a way that every droplet represents one unique reagent combination. We present a simple microcapillary technique able to generate such series of monodisperse water-in-oil droplets (with a frequency of up to 10 Hz) from a sample presented in an open well (e.g., a titerplate). Time-dependent variation of the well content results in microdroplets that represent time capsules of the composition of the source well. By preserving the spatial encoding of the droplets in tubing, each reactor is assigned an accurate concentration value. We used this approach to record kinetic time courses of the haloalkane dehalogenase DbjA and analyzed 150 combinations of enzyme/substrate/inhibitor in less than 5 min, resulting in conclusive Michaelis-Menten and inhibition curves. Avoiding chips and merely requiring two pumps, a magnetic plate with a stirrer, tubing, and a pipet tip, this easy-to-use device rivals the output of much more expensive liquid handling systems using a fraction (similar to 100-fold less) of the reagents consumed in microwell format.
机译:浓度依赖性分析是定量了解生物和化学系统的关键。在涉及浓度梯度的实验测试(例如抑制剂库筛选)中,数据点的数量以及每次测试所需的储备量与所需体积之间的比率决定了所获取信息的质量和效率。滴定板测定法是目前使用最广泛的形式,即使它们需要微升体积。微流体装置中皮微升至纳升油包水液滴中反应的区室化为大规模减少体积提供了解决方案。这项工作解决了产生微流体浓度梯度的挑战,即每个液滴代表一个独特的试剂组合。我们提出了一种简单的微毛细管技术,该技术能够从裸眼井中的样品(例如滴定板)中产生一系列这样的单分散油包水小滴(频率高达10 Hz)。孔含量随时间的变化会导致产生代表源孔组成的时间囊的微滴。通过保留管道中液滴的空间编码,可以为每个反应器分配一个准确的浓度值。我们用这种方法记录了卤代烷脱卤酶DbjA的动力学时间过程,并在不到5分钟的时间内分析了150种酶/底物/抑制剂的组合,得出了最终的Michaelis-Menten和抑制曲线。这种易于使用的设备避免了切屑,只需要两个泵,带有搅拌器的磁性板,管道和移液器吸头,就可以使用分数(大约少100倍)与更昂贵的液体处理系统相媲美。微孔格式消耗的试剂数量。

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