College of Chemistry and Chemical Engineering, Guangxi Normal University, Guilin 51004, China.
Anal Biochem. 2011 Apr 1;411(1):88-93. doi: 10.1016/j.ab.2010.12.025. Epub 2010 Dec 22.
A facile protocol to prepare highly effective and durable in-line enzyme bioreactors inside capillary electrophoresis (CE) columns was developed. To demonstrate the methodology, l-glutamic dehydrogenase (GLDH) was selected as the model enzyme. GLDH was first immobilized onto 38-nm-diameter gold nanoparticles (GNPs), and the functionalized GNPs were then assembled on the inner wall at the inlet end of the CE capillary treated with polyethyleneimine (PEI), producing an in-line GLDH bioreactor. Compared with a GLDH bioreactor prepared by immobilizing GLDH directly on PEI-treated capillary, the GNP-mediated bioreactor showed a higher enzymatic activity and a much better stability. The in-capillary enzyme bioreactor was proven to be very useful for screening of GLDH inhibitors deploying the GLDH-catalyzed α-ketoglutaric acid reaction. The screening assay was preliminarily validated by using a known GLDH inhibitor, namely perphenazine. A Z' factor value of 0.95 (n=10) was obtained, indicating that the screening results were highly reliable. Screening of GLDH inhibitors present in medicinal plant extracts by the proposed method was demonstrated. The inhibition percentages were found to be 53% for Radix scutellariae, 45% for Radix codonopsis, 37% for Radix paeoniae alba, and 0% for the other 22 extracts tested at a concentration of 0.6mg extract/ml.
一种在毛细管电泳(CE)柱内制备高效、耐用的在线酶生物反应器的简易方案已被开发。为了验证该方法,选择 l-谷氨酸脱氢酶(GLDH)作为模型酶。首先将 GLDH 固定在 38nm 直径的金纳米粒子(GNPs)上,然后将功能化的 GNPs 组装到经聚乙烯亚胺(PEI)处理的 CE 毛细管入口端的内壁上,形成在线 GLDH 生物反应器。与直接将 GLDH 固定在 PEI 处理的毛细管上制备的 GLDH 生物反应器相比,GNPs 介导的生物反应器表现出更高的酶活性和更好的稳定性。在毛细管内的酶生物反应器被证明在筛选 GLDH 抑制剂方面非常有用,该抑制剂采用 GLDH 催化的 α-酮戊二酸反应。该筛选测定法通过使用已知的 GLDH 抑制剂,即奋乃静,进行了初步验证。获得了 0.95 的 Z'因子值(n=10),表明筛选结果非常可靠。通过所提出的方法对药用植物提取物中的 GLDH 抑制剂进行了筛选。在 0.6mg 提取物/ml 的浓度下,对黄芩、党参、白芍的抑制率分别为 53%、45%、37%,而对其他 22 种提取物的抑制率为 0%。