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Increase of reaction rate and sensitivity of low-abundance enzyme assay using microanofluidic preconcentration chip

机译:使用微/纳流预浓缩芯片提高反应速率和低丰度酶测定的灵敏度

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摘要

We report a novel method of increasing both the reaction rate and the sensitivity of low-abundance enzyme assay using a microanofluidic preconcentration chip. The disposable preconcentration device made out of PDMS with a surface-patterned ion-selective membrane increases local enzyme/substrate concentrations for rapid monitoring of enzyme activity. As a model system, we used trypsin as the enzyme and BODIPY FL casein as the fluorogenic substrate. We demonstrated that the reaction rate of trypsin-BODIPY FL was significantly enhanced by increasing the local concentrations of both trypsin and BODIPY FL casein in the preconcentration chip. The reaction time required to turn over substrates at 1 ng/mL was only similar to 10 min compared to similar to 1 h without preconcentration, which demonstrates a significantly higher reaction rate through the increase of the concentrations of both the enzyme and substrate. Furthermore, trypsin activity can be measured down to a concentration level of 10 pg/mL, which is a similar to 100 fold enhancement in sensitivity compared to the result without the preconcentration step. This microanofluidic preconcentrator chip could be used as a generic micro reaction platform to study any enzyme-substrate systems, or other biochemical reaction systems in low concentration ranges.
机译:我们报告了一种使用微/纳米流体预浓缩芯片提高反应速率和低丰度酶测定灵敏度的新颖方法。由PDMS制成的具有表面图案化离子选择膜的一次性预浓缩装置可提高局部酶/底物的浓度,以快速监测酶的活性。作为模型系统,我们使用胰蛋白酶作为酶,使用BODIPY FL酪蛋白作为荧光底物。我们证明,通过增加预浓缩芯片中胰蛋白酶和BODIPY FL酪蛋白的局部浓度,可以显着提高胰蛋白酶-BODIPY FL的反应速率。与没有预浓缩的情况下1 h的反应时间相比,以1 ng / mL的速度翻转底物所需的反应时间仅与10 min相似,这表明通过增加酶和底物的浓度可以显着提高反应速度。此外,可以将胰蛋白酶活性降低到10 pg / mL的浓度水平,与没有预浓缩步骤的结果相比,其灵敏度提高了100倍。这种微/纳流体预浓缩器芯片可以用作通用的微反应平台,以研究任何酶-底物系统或低浓度范围内的其他生化反应系统。

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