Affinity membrane chromatography for the analysis and purification of proteins

被引:177
|
作者
Zou, HF [1 ]
Luo, QZ [1 ]
Zhou, DM [1 ]
机构
[1] Chinese Acad Sci, Dalian Inst Chem Phys, Natl Chromatog R&A Ctr, Dalian 116011, Peoples R China
来源
JOURNAL OF BIOCHEMICAL AND BIOPHYSICAL METHODS | 2001年 / 49卷 / 1-3期
基金
中国国家自然科学基金;
关键词
affinity chromatography; membrane stationary phases; monolithic columns; proteins;
D O I
10.1016/S0165-022X(01)00200-7
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Affinity chromatography is unique among separation methods as it is the only technique that permits the purification of proteins based on biological functions rather than individual physical or chemical properties. The high specificity of affinity chromatography is due to the strong interaction between the ligand and the proteins of interest. Membrane separation allows the processing of a large amount of sample in a relatively short time owing to its structure, which provides a system with rapid reaction kinetics. The integration of membrane and affinity chromatography provides a number of advantages over traditional affinity chromatography with porous-bead packed columns, especially with regard to time and recovery of activity. This review gives detailed descriptions of materials used as membrane substrates, preparation of basic membranes, coupling of affinity ligands to membrane supports, and categories of affinity membrane cartridges. It also summarizes the applications of cellulose/glycidyl methacrylate composite membranes for proteins separation developed in our laboratory. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:199 / 240
页数:42
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