Suppr超能文献

在表面改性的聚二甲基硅氧烷微流控装置上分离蛋白质。

Separation of proteins on surface-modified poly(dimethylsiloxane) microfluidic devices.

作者信息

Dou Yue-Hua, Bao Ning, Xu Jing-Juan, Meng Fei, Chen Hong-Yuan

机构信息

The State Key Laboratory of Coordination Chemistry, Institute of Analytical Science, Department of Chemistry, Nanjing University, Nanjing, P. R. China.

出版信息

Electrophoresis. 2004 Sep;25(17):3024-31. doi: 10.1002/elps.200405986.

Abstract

Separation and detection of proteins have been realized on nonionic surfactant-modified poly(dimethylsiloxane) (PDMS) microfabricated devices with end-column amperometric detection. The hydrophobic PDMS channels are turned into hydrophilic ones after being modified with Brij35 and facilitate the separation of proteins. The coating can remarkably reduce the adsorption of large protein molecules and is stable in the range of pH 6-12. The detection of proteins in such channels needs less rinsing time and thus efficiency is raised. Even large molecules of proteins can also be detected with better reproducibility and enhanced plate numbers. The relative standard deviation (RSD) of the migration time for glucose oxidase (GOD) is 2.2% (n = 19). Separation of GOD and myoglobin has been developed in modified channels. Predominant operational variables, such as the coating conditions, the concentration of surfactant and buffer, are studied in detail.

摘要

利用柱端安培检测法,已在非离子表面活性剂修饰的聚二甲基硅氧烷(PDMS)微加工器件上实现了蛋白质的分离与检测。经Brij35修饰后,疏水性的PDMS通道转变为亲水性通道,有利于蛋白质的分离。该涂层可显著减少大蛋白质分子的吸附,且在pH 6 - 12范围内稳定。在此类通道中检测蛋白质所需的冲洗时间更少,从而提高了效率。即使是大蛋白质分子也能被检测到,且具有更好的重现性和更高的塔板数。葡萄糖氧化酶(GOD)迁移时间的相对标准偏差(RSD)为2.2%(n = 19)。已在修饰通道中实现了GOD与肌红蛋白的分离。详细研究了主要操作变量,如涂层条件、表面活性剂和缓冲液的浓度。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验