Rendl Martin, Brandstetter Thomas, Rühe Jürgen
Laboratory for Chemistry and Physics of Interfaces, Department of Microsystems Engineering (IMTEK), University of Freiburg , Georges-Köhler-Allee 103, D-79110 Freiburg, Germany.
Anal Chem. 2013 Oct 15;85(20):9469-77. doi: 10.1021/ac401752j. Epub 2013 Oct 1.
In this article, we present a concept which uses liquid plugs as reaction volumes for heterogeneous assay reactions to facilitate time-resolved analysis of biomolecular reactions. For this purpose, the reaction is first compartmentalized to a train of many identical plugs. Therefore, we established a simple fluidic setup build from off-the-shelf available tubing and connectors. It permits reliable formation of plugs and successive dosing of further assay reagents to these compartments (plug volume <5% CV). The time course of the reaction is obtained by routing the plugs successively through a detector. Thereby, the arrival time of a given plug at the detector represents the reaction time of the overall reaction at that moment. Thus, each analyzed plug represents a discrete state of the overall reaction. With this approach, we can achieve a temporal resolution as small as one second, which hardly can be met by conventional analytical methods for analysis of endogenous biological compounds. For analysis of the content of the plugs, we developed a method which allows for heterogeneous assays in two-phase flow. For this purpose, functionalized superparamagnetic beads are enclosed in the plugs for specific binding of the assay product. Purification from supernatant species is achieved by transferring the beads with bound analyte across the phase boundary between aqueous plugs and water-immiscible carrier fluid. We demonstrate this assay principle exemplarily for a sandwich immunoassay (cytokine IL-8). Time-resolved analysis is validated by monitoring a cell-free in vitro expression reaction (turboGFP) in plugs and conventionally in bulk solution. We show that our approach allows for analyzing the entire course of a reaction in a single run. It permits kinetic studies of biological processes with significantly reduced experimental effort and consumption of costly reagents.
在本文中,我们提出了一种概念,即使用液塞作为异相分析反应的反应体积,以促进生物分子反应的时间分辨分析。为此,首先将反应分隔成一系列许多相同的液塞。因此,我们建立了一个简单的流体装置,由现成的管材和连接器构建而成。它能够可靠地形成液塞,并向这些隔室连续加入更多的分析试剂(液塞体积<5%CV)。通过使液塞依次通过检测器来获得反应的时间进程。由此,给定液塞到达检测器的时间代表了此时整个反应的反应时间。因此,每个分析的液塞代表了整个反应的一个离散状态。通过这种方法,我们可以实现低至一秒的时间分辨率,这是传统分析内源性生物化合物的方法几乎无法达到的。为了分析液塞的内容物,我们开发了一种允许在两相流中进行异相分析的方法。为此,将功能化的超顺磁性珠子封装在液塞中,用于分析产物的特异性结合。通过将结合有分析物的珠子转移穿过水性液塞和与水不混溶的载液之间的相界面,实现从上清液物质中纯化。我们以夹心免疫分析(细胞因子IL-8)为例展示了这种分析原理。通过监测液塞中以及传统的在大量溶液中的无细胞体外表达反应(turboGFP),对时间分辨分析进行了验证。我们表明,我们的方法允许在一次运行中分析反应的整个过程。它能够以显著减少的实验工作量和昂贵试剂的消耗对生物过程进行动力学研究。