Immobilized metal affinity composite membrane based on cellulose for separation of biopolymers

被引:16
作者
Yang, L [1 ]
Jia, LY [1 ]
Zou, HF [1 ]
Zhou, DM [1 ]
Zhang, YK [1 ]
机构
[1] Chinese Acad Sci, Dalian Inst Chem Phys, Natl Chromatog R&A Ctr, Dalian 116012, Peoples R China
来源
SCIENCE IN CHINA SERIES B-CHEMISTRY | 1998年 / 41卷 / 06期
基金
中国国家自然科学基金;
关键词
membrane; affinity chromatography; matrix; separation; biopolymers;
D O I
10.1007/BF02883021
中图分类号
O6 [化学];
学科分类号
0703 [化学];
摘要
A new iminodiacetic acid (IDA) type chelating membrane based on composite matrix formed by covalently coupling the polyglycidyl methacrylate to cotton cellulose fiber was developed. The study focused on the optimal conditions for the preparation of the membrane and the reaction of the chelating agent (iminodiacetic acid, IDA) with the matrix. The physical properties of the chelating membrane were tested by electron micrography and BET surface area instrument. The relationship between flow-rate and backpressure was almost linear. Adsorption isotherm of protein on Cu2+ - IDA membrane was determined by batch experiments. The dissociation constants and the maximum adsorption capacity were obtained. The results of affinity purification of human serum albumin and bovine liver catalase on membrane are comparable with those on gel chromatography presented in literature. The separations performed on the membrane chromatography, however, were 3-5 times faster than those on gel chromatography. The immobilized metal composite membrane was also successfully used in HPLC for rapid analysis of protein. Thus, the composite membrane reported here, with low backpressure, low cost and long service-life, is quite suitable for rapid and large scale affinity purification and HPLC analysis of biopolymers.
引用
收藏
页码:596 / 605
页数:10
相关论文
共 13 条
[1]
PURIFICATION OF COMMERCIAL HUMAN-ALBUMIN ON IMMOBILIZED IDA-NI2+ [J].
ANDERSSON, L ;
SULKOWSKI, E ;
PORATH, J .
JOURNAL OF CHROMATOGRAPHY-BIOMEDICAL APPLICATIONS, 1987, 421 (01) :141-146
[2]
BEAD CELLULOSE DERIVATIVES AS SUPPORTS FOR IMMOBILIZATION AND CHROMATOGRAPHIC PURIFICATION OF PROTEINS [J].
BOEDEN, HF ;
POMMERENING, K ;
BECKER, M ;
RUPPRICH, C ;
HOLTZHAUER, M ;
LOTH, F ;
MULLER, R ;
BERTRAM, D .
JOURNAL OF CHROMATOGRAPHY, 1991, 552 (1-2) :389-414
[3]
ISOLATION AND CHARACTERIZATION OF CATALASE FROM PENICILLIUM-CHRYSOGENUM [J].
CHAGA, GS ;
MEDIN, AS ;
CHAGA, SG ;
PORATH, JO .
JOURNAL OF CHROMATOGRAPHY, 1992, 604 (01) :177-183
[4]
FENG WX, 1989, BIOCH TECHNOLOGY, P193
[5]
PURIFICATION OF UROKINASE BY COMBINED CATION EXCHANGER AND AFFINITY CHROMATOGRAPHIC CARTRIDGES [J].
HOU, KC ;
ZANIEWSKI, R .
JOURNAL OF CHROMATOGRAPHY-BIOMEDICAL APPLICATIONS, 1990, 525 (02) :297-306
[6]
Protein interaction with immobilized metal ion affinity ligands under high ionic strength conditions [J].
Jiang, W ;
Hearn, MTW .
ANALYTICAL BIOCHEMISTRY, 1996, 242 (01) :45-54
[7]
HIGH-PERFORMANCE MEMBRANE CHROMATOGRAPHY OF SERUM AND PLASMA-MEMBRANE PROTEINS [J].
JOSIC, D ;
REUSCH, J ;
LOSTER, K ;
BAUM, O ;
REUTTER, W .
JOURNAL OF CHROMATOGRAPHY, 1992, 590 (01) :59-76
[8]
LIU GQ, 1993, BIOENGINEERING DOWNS, P260
[9]
MALAKIAN A, 1993, AM LAB, V2, pP40
[10]
MEMBRANE-BASED RECEPTOR AFFINITY-CHROMATOGRAPHY [J].
NACHMAN, M ;
AZAD, ARM ;
BAILON, P .
JOURNAL OF CHROMATOGRAPHY, 1992, 597 (1-2) :155-166