State Key Laboratory of Analytical Chemistry for Life Sciences, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing 210093, China.
Lab Chip. 2013 Apr 21;13(8):1546-53. doi: 10.1039/c3lc41319e.
The investigation of enzyme reaction kinetics in nanoconfined spaces mimicking the conditions in living systems is of great significance. Here, a nanofluidics chip integrated with an electrochemical detector has been designed for studying "free state" enzyme reaction kinetics in nanoconfinement. The nanofluidics chip is fabricated using the UV-ablation technique developed in our group. The enzyme and substrate solutions are simultaneously supplied from two single streams into a nanochannel through a Y-shaped junction. The laminar flow forms in the front of the nanochannel, then the two liquids fully mix at their downstream where a homogeneous enzyme reaction occurs. The "free state" enzyme reaction kinetics in nanoconfinement can thus be investigated in this laminar flow based nanofluidics device. For demonstration, glucose oxidase (GOx) is chosen as the model enzyme, which catalyzes the oxidation of beta-d-glucose. The reaction product hydrogen peroxide (H2O2) can be electrochemically detected by a microelectrode aligning to the end of nanochannel. The steady-state electrochemical current responding to various glucose concentrations is used to evaluate the activity of the "free state" GOx under nanoconfinement conditions. The effect of liquid flow rate, enzyme concentration, and nanoconfinement on reaction kinetics has been studied in detail. Results show that the "free state" GOx activity increases significantly compared to the immobilized enzyme and bath system, and the GOx reaction rate in the nanochannel is two-fold faster than that in bulk solution, demonstrating the importance of "free state" and spatial confinement for the enzyme reaction kinetics. The present approach provides an effective method for exploiting the "free state" enzyme activity in nanospatial confinement.
模拟生命体系条件下的酶反应动力学研究在纳米受限空间中具有重要意义。在这里,设计了一种带有电化学检测器的纳流控芯片,用于研究纳米受限条件下的“自由态”酶反应动力学。纳流控芯片采用我们小组开发的紫外消融技术制备。酶和底物溶液通过 Y 型接头同时从两个单流道供应到纳米通道中。在纳米通道的前端形成层流,然后两种液体在下游完全混合,发生均相酶反应。因此,可以在这种基于层流的纳流控装置中研究纳米受限空间中的“自由态”酶反应动力学。为了演示,选择葡萄糖氧化酶(GOx)作为模型酶,它催化β-D-葡萄糖的氧化。反应产物过氧化氢(H2O2)可以通过与纳米通道末端对齐的微电极电化学检测。稳态电化学电流对各种葡萄糖浓度的响应用于评估纳米受限条件下“自由态”GOx 的活性。详细研究了液体流速、酶浓度和纳米受限对反应动力学的影响。结果表明,与固定化酶和浴体系相比,“自由态”GOx 的活性显著增加,纳米通道中的 GOx 反应速率比体相溶液中的反应速率快两倍,这表明“自由态”和空间受限对酶反应动力学的重要性。本方法为开发纳米空间限域内“自由态”酶活性提供了一种有效方法。