Preparation of affinity membranes using polymer phase separation and azido-containing surfactants

被引:6
作者
Morita, Kenta [1 ]
Takeda, Shinano [1 ]
Yunoki, Ayumi [1 ]
Tsuchii, Takane [1 ]
Tanaka, Tsutomu [1 ]
Maruyama, Tatsuo [1 ]
机构
[1] Kobe Univ, Grad Sch Engn, Dept Chem Sci & Engn, Nada Ku, 1-1 Rokkodai, Kobe, Hyogo 6578501, Japan
关键词
Affinity membrane; Antibiotic; Molecular recognition; Protein; Selective separation; Surface immobilization; ULTRAFILTRATION MEMBRANES; PURIFICATION; PROTEINS; CHROMATOGRAPHY; MICROFILTRATION; ANTIBIOTICS; MORPHOLOGY; BRUSHES; TRENDS; ACID;
D O I
10.1016/j.colsurfa.2020.125802
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We propose a novel approach to prepare affinity membranes using azido-containing surfactants and click chemistry. Porous polymeric membranes were prepared using cellulose acetate via polymer phase separation in the presence of azido-containing surfactants. Thermally induced phase separation and nonsolvent-induced phase separation were used for membrane preparation. The azido groups displayed on the membrane surfaces were conjugated with nitrilotriacetic acid via Huisgen 1,3-dipolar cycloaddition to prepare membranes that displayed affinity toward a hexahistidine-tagged protein. Two types of phase separation successfully produced porous membranes with different microstructures but showed similar separation performances. In place of nitrilotriacetic acid, D-Ala-D-Ala was conjugated to the surface of the azido-functionalized membrane. The membranes functionalized with D-Ala-D-Ala showed high affinity toward vancomycin. The present approach leads to facile surface functionalization of polymeric materials and produces affinity membranes displaying various types of ligands on their surfaces.
引用
收藏
页数:7
相关论文
共 45 条
[1]   Challenges and trends in bioseparations [J].
Asenjo, Juan A. ;
Andrews, Barbara A. .
JOURNAL OF CHEMICAL TECHNOLOGY AND BIOTECHNOLOGY, 2008, 83 (02) :117-120
[2]   Membrane adsorbers as purification tools for monoclonal antibody purification [J].
Boi, Cristiana .
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2007, 848 (01) :19-27
[3]   Cell cycle molecular targets in novel anticancer drug discovery [J].
Buolamwini, JK .
CURRENT PHARMACEUTICAL DESIGN, 2000, 6 (04) :379-392
[4]  
de la Torre B.G., 2020, MOLECULES, V25
[5]   Effect of surface morphology on membrane fouling by humic acid with the use of cellulose acetate butyrate hollow fiber membranes [J].
Fu, Xunyao ;
Maruyama, Tatsuo ;
Sotani, Tomohiro ;
Matsuyama, Hideto .
JOURNAL OF MEMBRANE SCIENCE, 2008, 320 (1-2) :483-491
[6]   Enhancement in hydrophilicity of different polymer phase-inversion ultrafiltration membranes by introducing PEG/Al2O3 nanoparticles [J].
Garcia-Ivars, Jorge ;
Alcaina-Miranda, Maria-Isabel ;
Iborra-Clar, Maria-Isabel ;
Mendoza-Roca, Jose-Antonio ;
Pastor-Alcaniz, Laura .
SEPARATION AND PURIFICATION TECHNOLOGY, 2014, 128 :45-57
[7]   Liquid chromatography of recombinant proteins and protein drugs [J].
Geng Xindu ;
Wang Lili .
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2008, 866 (1-2) :133-153
[8]   Enzyme assays for high-throughput screening [J].
Goddard, JP ;
Reymond, JL .
CURRENT OPINION IN BIOTECHNOLOGY, 2004, 15 (04) :314-322
[9]   Liquid-fluid contact angle measurements on hydrophilic cellulosic materials [J].
Grundke, K ;
Bogumil, T ;
Werner, C ;
Janke, A ;
Poschel, K ;
Jacobasch, HJ .
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS, 1996, 116 (1-2) :79-91
[10]   Membrane fouling during microfiltration of protein mixtures [J].
Guell, C ;
Davis, RH .
JOURNAL OF MEMBRANE SCIENCE, 1996, 119 (02) :269-284