Thin-layer ion-exchange chromatography of proteins

被引:10
作者
Luo, QL
Andrade, JD
Caldwell, KD
机构
[1] Univ Utah, Dept Bioengn, Salt Lake City, UT 84112 USA
[2] Univ Utah, Dept Mat Sci & Engn, Salt Lake City, UT 84112 USA
关键词
adsorption isotherms; proteins; albumin; transferrin; lactoferrin; lysozyme;
D O I
10.1016/S0021-9673(98)00286-6
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Thin-layer chromatography (TLC) is one of the simplest and most convenient techniques to separate small molecules. Of a variety of TLC separation modes, only size-exclusion was successfully used to separate proteins. In this paper, adsorption-TLC was used to separate proteins. The net charges were calculated for four model proteins, albumin, transferrin, lactoferrin and lysozyme, under different pH values. The suitable pH values for separation were determined according to the results from such calculations. Then, the adsorption isotherms of the four proteins were measured to deduce the ionic strength for appropriate elution conditions. Optimal conditions, 0.01 M bicine and pH 8.50, and a three-step elution process (Ist step 0.01 M NaCl, 2nd 0.025 M NaCl, and 3rd 0.10 M NaCl), were obtained. Finally, the four model proteins were successfully separated under these elution conditions. (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:97 / 105
页数:9
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