Suppr超能文献

一种基于金纳米粒子的酶生物反应器,通过毛细管电泳进行抑制剂筛选。

A gold nanoparticle-mediated enzyme bioreactor for inhibitor screening by capillary electrophoresis.

机构信息

College of Chemistry and Chemical Engineering, Guangxi Normal University, Guilin 51004, China.

出版信息

Anal Biochem. 2011 Apr 1;411(1):88-93. doi: 10.1016/j.ab.2010.12.025. Epub 2010 Dec 22.

Abstract

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.

摘要

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%。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7ee/3039056/a0df8b952724/nihms260940f1.jpg

相似文献

本文引用的文献

3
Bioconjugation and characterisation of gold colloid-labelled proteins.金胶标记蛋白的生物偶联和特性分析。
J Immunol Methods. 2010 Apr 30;356(1-2):60-9. doi: 10.1016/j.jim.2010.02.007. Epub 2010 Feb 24.
6
Understanding enzyme immobilisation.理解酶的固定化。
Chem Soc Rev. 2009 Feb;38(2):453-68. doi: 10.1039/b711564b. Epub 2008 Dec 9.
7
Development of high performance liquid chromatography with immobilized enzyme onto magnetic nanospheres for screening enzyme inhibitor.
J Chromatogr B Analyt Technol Biomed Life Sci. 2008 Aug 1;871(1):67-71. doi: 10.1016/j.jchromb.2008.06.036. Epub 2008 Jun 27.
10
New aspects of natural products in drug discovery.天然产物在药物发现中的新进展。
Trends Microbiol. 2007 Jun;15(6):279-89. doi: 10.1016/j.tim.2007.04.001. Epub 2007 Apr 11.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验