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将微孔与纳升隔室相连接:一种为液滴中的定量生化分析生成高分辨率浓度梯度的采样器。

Interfacing microwells with nanoliter compartments: a sampler generating high-resolution concentration gradients for quantitative biochemical analyses in droplets.

作者信息

Gielen Fabrice, Buryska Tomas, Van Vliet Liisa, Butz Maren, Damborsky Jiri, Prokop Zbynek, Hollfelder Florian

机构信息

Department of Biochemistry, University of Cambridge , 80 Tennis Court Road, Cambridge, CB2 1GA, United Kingdom.

出版信息

Anal Chem. 2015 Jan 6;87(1):624-32. doi: 10.1021/ac503336g. Epub 2014 Dec 12.

DOI:10.1021/ac503336g
PMID:25496166
Abstract

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 (∼100-fold less) of the reagents consumed in microwell format.

摘要

浓度依赖性分析是定量理解生物和化学系统的关键。在涉及浓度梯度的实验测试中,如抑制剂文库筛选,数据点的数量以及储备液体积与每次测试所需体积之间的比例决定了所获信息的质量和效率。目前,滴定板测定法是使用最广泛的形式,尽管它们需要微升体积。在微流控装置中,将反应分隔在皮升至纳升的油包水微滴中,为大幅减少体积提供了解决方案。这项工作解决了以一种每个微滴代表一种独特试剂组合的方式产生基于微流控的浓度梯度的挑战。我们提出了一种简单的微毛细管技术,能够从开放式孔(如滴定板)中呈现的样品生成这样一系列单分散的油包水微滴(频率高达10赫兹)。孔内容物随时间的变化产生代表源孔组成的时间胶囊的微滴。通过在管道中保留微滴的空间编码,每个反应器被赋予一个准确的浓度值。我们使用这种方法记录了卤代烷脱卤酶DbjA的动力学时间进程,并在不到5分钟的时间内分析了150种酶/底物/抑制剂组合,得到了确凿的米氏和抑制曲线。该易于使用的装置无需芯片,仅需两个泵、一个带搅拌器的磁性板、管道和一个移液器吸头,其输出可与更昂贵的液体处理系统相媲美,且使用的试剂仅为微孔形式消耗试剂的一小部分(约少100倍)。

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