Polymer-based monolithic microcolumns for hydrophobic interaction chromatography of proteins

被引:58
作者
Hemström, P
Nordborg, A
Irgum, K [1 ]
Svec, F
Fréchet, JMJ
机构
[1] Umea Univ, Dept Chem, S-90187 Umea, Sweden
[2] Univ Calif Berkeley, Dept Chem, Berkeley, CA 94720 USA
关键词
capillary; column; HIC; hydrophobic interaction chromatography; monolith; protein separation;
D O I
10.1002/jssc.200500239
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Monolithic capillary columns for hydrophobic, interaction chromatography (HIC) have been prepared by thermally initiated, single-step in situ polymerization of mixtures of monovinyl monomers including butyl methacrylate and/or 2-hydroxyethyl methacrylate, with a divinyl. crosslinker glycerol dimethacrylate or 1,4-butanediol dimethacrylate using two different porogen systems. Two porogenic solvent mixtures were used; one "hydrophilic", consisting of water, butanediol, and proparrol, and one "hydrophobic," comprising dodecanol and cyclohexanol. The porous structures of the monoliths were characterized and their performance was demonstrated with a separation of a mixture of myoglobin, ribonuclease A, and lysozyme under conditions typical of HIC.
引用
收藏
页码:25 / 32
页数:8
相关论文
共 40 条
[1]   PREFERENTIAL INTERACTIONS OF PROTEINS WITH SALTS IN CONCENTRATED-SOLUTIONS [J].
ARAKAWA, T ;
TIMASHEFF, SN .
BIOCHEMISTRY, 1982, 21 (25) :6545-6552
[2]   PREFERENTIAL INTERACTIONS DETERMINE PROTEIN SOLUBILITY IN 3-COMPONENT SOLUTIONS - THE MGCL2 SYSTEM [J].
ARAKAWA, T ;
BHAT, R ;
TIMASHEFF, SN .
BIOCHEMISTRY, 1990, 29 (07) :1914-1923
[3]  
ARAKAWA T, 1985, BIOCHEMISTRY-US, V24, P6762
[4]  
Arshady R., 1983, REACT POLYM ION EXCH, V1, P159
[5]   Effect of salts and temperature on the adsorption of bovine serum albumin on polypropylene glycol-Sepharose under linear and overloaded chromatographic conditions [J].
Dias-Cabral, AC ;
Queiroz, JA ;
Pinto, NG .
JOURNAL OF CHROMATOGRAPHY A, 2003, 1018 (02) :137-153
[6]   Studies on the retention of plasmid DNA and Escherichia coli nucleic acids by hydrophobic interaction chromatography [J].
Diogo, MM ;
Queiroz, JA ;
Prazeres, DMF .
BIOSEPARATION, 2001, 10 (4-5) :211-220
[7]  
ELRASSI Z, 1986, J LIQ CHROMATOGR, V9, P3245
[8]   Study of hydrophobic interaction adsorption of bovine serum albumin under overloaded conditions using flow microcalorimetry [J].
Esquibel-King, MA ;
Dias-Cabral, AC ;
Queiroz, JA ;
Pinto, NG .
JOURNAL OF CHROMATOGRAPHY A, 1999, 865 (1-2) :111-122
[9]   SOLUTE AND MOBILE PHASE CONTRIBUTIONS TO RETENTION IN HYDROPHOBIC INTERACTION CHROMATOGRAPHY OF PROTEINS [J].
FAUSNAUGH, JL ;
REGNIER, FE .
JOURNAL OF CHROMATOGRAPHY, 1986, 359 :131-146
[10]   COMPARISON OF HYDROPHOBIC-INTERACTION AND REVERSED-PHASE CHROMATOGRAPHY OF PROTEINS [J].
FAUSNAUGH, JL ;
KENNEDY, LA ;
REGNIER, FE .
JOURNAL OF CHROMATOGRAPHY, 1984, 317 (DEC) :141-155