Monoliths as stationary phases for separation of proteins and polynucleotides and enzymatic conversion

被引:178
作者
Josic, D
Buchacher, A
Jungbauer, A
机构
[1] Octapharma Pharmzeut Prod GesmbH, A-1100 Vienna, Austria
[2] Univ Agr Sci, Inst Appl Microbiol, A-1190 Vienna, Austria
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2001年 / 752卷 / 02期
关键词
monoliths; enzymatic conversion; proteins; polynucleotides;
D O I
10.1016/S0378-4347(00)00499-0
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Monoliths are considered as a novel generation of stationary phases. They were applied for capillary electrochromatography and liquid chromatography exploiting every action principle such as ion-exchange, affinity recognition, reversed-phase, and hydrophobic interaction. The fast separation was explained by convective transport of the solutes through the bed. The contribution of this mode of transport is similarly explained as done for the beds packed with particles with gigapores. For monolithic beds, the concept of an ultrashort bed was frequently used. This mode of operation allows very short separation time. In many cases a gradient elution is necessary to achieve separation. Examples of applications for protein and polynucleotide separation performed on monoliths are given. Enzymatic conversion was described showing the examples of several immobilzed enzymes. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:191 / 205
页数:15
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