Institute of Scientific and Industrial Research, Osaka University, Mihogaoka, 8-1, Ibaraki, Osaka 567-0047, Japan.
Lab Chip. 2010 Dec 21;10(24):3355-62. doi: 10.1039/c0lc00062k. Epub 2010 Oct 28.
The enzyme assay in a femtoliter chamber array is a simple and efficient method for concentrating the reaction product; it greatly improves the detection sensitivity down to the single-molecule level. However, in previous methods, controlling the initiation and termination of the reaction in each chamber is difficult once enclosed. Furthermore, the recovery of the enzyme and product is also difficult. To overcome these drawbacks, we developed a femtoliter droplet array in which the individual droplets are fixed on the substrate and are directly accessible from outside. A hydrophilic-in-hydrophobic micropatterned surface was used for the preparation of the droplets. When the aqueous solution on the surface is exchanged with oil, the hydrophilic surface retains the aqueous solution, and more than 10(6) dome-shaped droplets that are usable for further assay can be prepared simultaneously. The curvature radius of the droplet obeys the Young-Laplace equation, and the volume can be precisely controlled by the micropipette, which applies pressure into the droplet. Changing the pressure makes the addition, collection, and exchange of the aqueous content for individual droplets possible. Using these advantages, we successfully measured the kinetic parameters of the single-molecule enzyme β-galactosidase and rotary motor protein F(1)-ATPase enclosed in a droplet.
在飞升级腔室阵列中的酶分析是浓缩反应产物的一种简单而有效的方法;它极大地提高了检测灵敏度,达到了单分子水平。然而,在以前的方法中,一旦封闭,控制每个腔室中反应的开始和结束是很困难的。此外,酶和产物的回收也很困难。为了克服这些缺点,我们开发了一种飞升级液滴阵列,其中各个液滴固定在基底上并且可以从外部直接接触。亲水性-疏水性微图案化表面用于制备液滴。当表面上的水溶液与油交换时,亲水表面保留水溶液,并且可以同时制备超过 10(6)个可用于进一步分析的半球形液滴。液滴的曲率半径遵循杨-拉普拉斯方程,并且体积可以通过施加压力进入液滴的微量移液器精确控制。改变压力使得可以向各个液滴添加、收集和交换水相内容物。利用这些优势,我们成功地测量了单个酶β-半乳糖苷酶和旋转马达蛋白 F(1)-ATPase 在液滴中包封的动力学参数。