Song Helen, Ismagilov Rustem F
Department of Chemistry, The University of Chicago, 5735 South Ellis Avenue, Chicago, IL 60637, USA.
J Am Chem Soc. 2003 Nov 26;125(47):14613-9. doi: 10.1021/ja0354566.
This paper describes a microfluidic chip for performing kinetic measurements with better than millisecond resolution. Rapid kinetic measurements in microfluidic systems are complicated by two problems: mixing is slow and dispersion is large. These problems also complicate biochemical assays performed in microfluidic chips. We have recently shown (Song, H.; Tice, J. D.; Ismagilov, R. F. Angew. Chem., Int. Ed. 2003, 42, 768-772) how multiphase fluid flow in microchannels can be used to address both problems by transporting the reagents inside aqueous droplets (plugs) surrounded by an immiscible fluid. Here, this droplet-based microfluidic system was used to extract kinetic parameters of an enzymatic reaction. Rapid single-turnover kinetics of ribonuclease A (RNase A) was measured with better than millisecond resolution using sub-microliter volumes of solutions. To obtain the single-turnover rate constant (k = 1100 +/- 250 s(-1)), four new features for this microfluidics platform were demonstrated: (i) rapid on-chip dilution, (ii) multiple time range access, (iii) biocompatibility with RNase A, and (iv) explicit treatment of mixing for improving time resolution of the system. These features are discussed using kinetics of RNase A. From fluorescent images integrated for 2-4 s, each kinetic profile can be obtained using less than 150 nL of solutions of reagents because this system relies on chaotic advection inside moving droplets rather than on turbulence to achieve rapid mixing. Fabrication of these devices in PDMS is straightforward and no specialized equipment, except for a standard microscope with a CCD camera, is needed to run the experiments. This microfluidic platform could serve as an inexpensive and economical complement to stopped-flow methods for a broad range of time-resolved experiments and assays in chemistry and biochemistry.
本文介绍了一种用于进行动力学测量的微流控芯片,其分辨率优于毫秒级。微流控系统中的快速动力学测量因两个问题而变得复杂:混合缓慢且扩散较大。这些问题也使在微流控芯片中进行的生化分析变得复杂。我们最近已经表明(宋,H.;蒂斯,J. D.;伊斯马吉洛夫,R. F.《德国应用化学》,国际版,2003年,42卷,768 - 772页),微通道中的多相流体流动如何通过在由不混溶流体包围的水滴(塞子)内输送试剂来解决这两个问题。在此,基于液滴的微流控系统被用于提取酶促反应的动力学参数。使用亚微升体积的溶液,以优于毫秒级的分辨率测量了核糖核酸酶A(RNase A)的快速单周转动力学。为了获得单周转速率常数(k = 1100 ± 250 s⁻¹),展示了该微流控平台的四个新特性:(i)芯片上的快速稀释,(ii)多时间范围访问,(iii)与RNase A的生物相容性,以及(iv)对混合进行明确处理以提高系统的时间分辨率。使用RNase A的动力学对这些特性进行了讨论。从积分2 - 4秒的荧光图像中,每个动力学曲线可以使用少于150 nL的试剂溶液获得,因为该系统依靠移动液滴内的混沌平流而非湍流来实现快速混合。这些装置在聚二甲基硅氧烷(PDMS)中的制造很简单,除了带有电荷耦合器件(CCD)相机的标准显微镜外,运行实验不需要专门的设备。对于化学和生物化学中广泛的时间分辨实验和分析,这个微流控平台可以作为停流方法的一种廉价且经济的补充。