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Frontiers of Chemical Science and Engineering

ISSN 2095-0179

ISSN 2095-0187(Online)

CN 11-5981/TQ

Postal Subscription Code 80-969

2018 Impact Factor: 2.809

Front Chem Eng Chin    2009, Vol. 3 Issue (3) : 229-234    https://doi.org/10.1007/s11705-009-0213-6
RESEARCH ARTICLE
Protein adsorption in two-dimensional electrochromatography packed with superporous and microporous cellulose beads
Dongmei WANG1,2, Guodong JIA1, Liang XU1, Xiaoyan DONG1, Yan SUN1()
1. Department of Biochemical Engineering, School of Chemical Engineering and Technology, Tianjin University, Tianjin 300072, China; 2. School of Pharmaceutical Sciences, Tianjin Medical University, Tianjin 300070, China
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Abstract

Anion-exchange superporous cellulose (DEAE-SC) and microporous cellulose (DEAE-MC) adsorbents were packed in an electrochromatographic column, and the effect of external electric field (eEF) on the dynamic adsorption was investigated. The column was designed to provide longitudinal, transverse or 2-dimensional (2D) eEF. It was found that the electro-kinetic effect caused by the introduction of an electric field played an important role in the dynamic adsorption of bovine serum albumin to the adsorbents. The dynamic binding capacity (DBC) in the presence of 2D eEF was higher than in the presence of a one-dimensional eEF. The effect of flow velocity on the DBC of the two adsorbents was also demonstrated. It was found that the effect of electric field on the DEAE-MC column was more remarkable than that on the DEAE-SC column at the same flow rate, whereas the DEAE-SC column showed higher DBC and adsorption efficiency (AE) than the DEAE-MC column. With increasing flow rate, the DEAE-SC column could still offer high DBC and AE in the presence of the 2D eEF. For example, a DBC of 21.4 mg/mL and an AE of 57.7% were obtained even at a flow rate as high as 900 cm/h. The results indicate that the 2D electrochromatography packed with the superporous cellulose adsorbent is promising for high-speed protein chromatography.

Keywords electrochromatography      two-dimensional electric field      dynamic binding capacity      superporous cellulose bead      protein     
Corresponding Author(s): SUN Yan,Email:ysun@tju.edu.cn   
Issue Date: 05 September 2009
 Cite this article:   
Dongmei WANG,Guodong JIA,Liang XU, et al. Protein adsorption in two-dimensional electrochromatography packed with superporous and microporous cellulose beads[J]. Front Chem Eng Chin, 2009, 3(3): 229-234.
 URL:  
https://academic.hep.com.cn/fcse/EN/10.1007/s11705-009-0213-6
https://academic.hep.com.cn/fcse/EN/Y2009/V3/I3/229
Fig.1  Structure of the electrochromatographic column with 2D eEF
1. longitudinal electrode compartments; 2. transverse electrode compartments; 3. mini feeding compartments; 4. central gel compartment
adsorbentDEAE-MCDEAE-SC
effective porosity, ?p (-)0.420.51
ion-exchange capacity /(μmol?mL-1)111.496.9
dp /μm8588
qm /( mg·mL-1 wet bead)48.1537.12
Kd /(mg?mL-1)0.00550.0053
Tab.1  Parameters of physical properties and adsorption equilibria
electric fieldDBC /( mg?mL-1)AE /%δ10
MCSCMCSCMCSC
no eEF7.2019.714.953.11.001.00
longitudinal, 10 mA 8.4023.217.462.51.171.18
transverse, 80 mA 10.523.621.863.61.461.20
2D15.326.131.770.42.131.32
Tab.2  Comparison of between the different types of eEF on the column packed with DEAE-MC and DEAE-SC at the flow rate of 600 cm/h
Fig.2  Breakthrough curves of BSA on DEAE-SC (a) and DEAE-MC (b) with different types of eEF. L, longitudinal electric field; T, transverse electric field at 600 cm/h. The mobile phase was buffer A (3.9 mmol/L Tris, 47 mmol/L Gly, 5 mmol/L NaCl, pH 8.2). Sample solution was 2 mg/mL BSA prepared with buffer A
flow rate /(cm?h-1)electric fieldDBC /(mg?mL-1)AE /%δ10
MCSCMCSCMCSC
300no eEF20.122.341.760.11.671.21
2D33.627.069.772.8
600no eEF7.2019.714.953.12.131.32
2D15.326.131.770.4
900no eEF6.1315.212.741.01.761.41
2D10.821.422.457.7
Tab.3  Comparison of DBC, AE and at different flow velocity in 2D eEF applied column packed with DEAE-MC and DEAE-SC
Fig.3  Breakthrough curves of BSA on DEAE-MC and DEAE-SC columns with 2D eEF at 600 cm/h. The mobile phase was buffer A (3.9 mmol/L Tris, 47 mmol/L Gly, 5 mmol/L NaCl, pH 8.2). Sample solution was 2 mg/mL BSA prepared with buffer A
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