Human serum albumin chromatography by Cibacron Blue F3GA-derived microporous polyamide hollow-fiber affinity membranes

被引:60
作者
Kassab, A [1 ]
Yavuz, H [1 ]
Odabasi, M [1 ]
Denizli, A [1 ]
机构
[1] Univ Hacettepe, Dept Chem, Div Biochem, TR-06100 Ankara, Turkey
来源
JOURNAL OF CHROMATOGRAPHY B | 2000年 / 746卷 / 02期
关键词
polyamide hollow-fibre; affinity membranes; human serum albumin; Cibacron Blue F3GA;
D O I
10.1016/S0378-4347(00)00311-X
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
An affinity dye ligand, Cibacron Blue F3GA was covalently attached onto commercially available microporous polyamide hollow-fibre membranes for human serum albumin (HSA) adsorption from both aqueous solutions and human plasma. Different amounts of Cibacron Blue F3GA were incorporated on the polyamide hollow-fibres by changing the dye attachment conditions, i.e. initial dye concentration, addition of sodium carbonate and sodium chloride. The maximum amount of Cibacron Blue F3GA attachment was obtained at 42.5 mu mol g(-1) when the hollow-fibres were treated with 3 M HCl for 30 min before performing the dye attachment. HSA adsorption onto unmodified and Cibacron Blue F3GA-derived polyamide hollow-fibre membranes was investigated batchwise. The non-specific adsorption of HSA was very low (6.0 mg g(-1) hollow-fibre). Cibacron Blue F3GA attachment onto the hollow-fibres significantly increased the HSA adsorption (147 mg g(-1) hollow-fibre). The maximum HSA adsorption was observed at pH 5.0. Higher HSA adsorption was observed from human plasma (230 mg HSA g(-1) hollow-fibre). Desorption of HSA from Cibacron Blue F3GA derived hollow-fibres was obtained using 0.1 M Tris-HCl buffer containing 0.5 M NaSCN or 1.0 M NaCl. High desorption ratios (up to 98% of the adsorbed HSA) were observed. It was possible to reuse Cibacron Blue F3GA derived polyamide hollow-fibre without significant decreases in the adsorption capacities. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:123 / 132
页数:10
相关论文
共 48 条
[1]   INTERACTION OF CIBACRON BLUE 3G-A AND RELATED DYES WITH NUCLEOTIDE-REQUIRING ENZYMES [J].
BEISSNER, RS ;
RUDOLPH, FB .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1978, 189 (01) :76-80
[2]  
Boyer P M, 1993, Adv Biochem Eng Biotechnol, V49, P1
[3]   EFFECTS OF LIGAND CONCENTRATION ON PROTEIN ADSORPTION IN DYE LIGAND ADSORBENTS [J].
BOYER, PM ;
HSU, JT .
CHEMICAL ENGINEERING SCIENCE, 1992, 47 (01) :241-251
[4]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[5]   PREDICTION OF THE PERFORMANCE OF PREPARATIVE AFFINITY-CHROMATOGRAPHY [J].
CHASE, HA .
JOURNAL OF CHROMATOGRAPHY, 1984, 297 (AUG) :179-202
[6]  
CLAUSS A., 1957, ACTA HAEMATOL, V17, P237
[7]   PREPARATION AND PROPERTIES OF SERUM AND PLASMA PROTEINS .4. A SYSTEM FOR THE SEPARATION INTO FRACTIONS OF THE PROTEIN AND LIPOPROTEIN COMPONENTS OF BIOLOGICAL TISSUES AND FLUIDS [J].
COHN, EJ ;
STRONG, LE ;
HUGHES, WL ;
MULFORD, DJ ;
ASHWORTH, JN ;
MELIN, M ;
TAYLOR, HL .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1946, 68 (03) :459-475
[8]   Diamine-plasma treated and Cu(II)-incorporated poly(hydroxyethylmethacrylate) microbeads for albumin adsorption [J].
Denizli, A ;
Denizli, F ;
Piskin, E .
JOURNAL OF BIOMATERIALS SCIENCE-POLYMER EDITION, 1999, 10 (03) :305-318
[9]   Cibacron blue F3G-A attached poly(vinyl alcohol) particles for specific albumin adsorption [J].
Denizli, A ;
Tuncel, A ;
Kozluca, A ;
Ecevit, K ;
Piskin, E .
SEPARATION SCIENCE AND TECHNOLOGY, 1997, 32 (05) :1003-1015
[10]  
Denizli A, 1999, J APPL POLYM SCI, V74, P2803, DOI 10.1002/(SICI)1097-4628(19991213)74:12<2803::AID-APP3>3.3.CO