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制备规模的循环式pH偏置二元等电聚焦分离

Preparative-scale, recirculating, pH-biased binary isoelectric trapping separations.

作者信息

Shave Evan, Vigh Gyula

机构信息

Chemistry Department, Texas A&M University, College Station, TX 77842, USA.

出版信息

Electrophoresis. 2004 Jan;25(2):381-7. doi: 10.1002/elps.200305752.

Abstract

In order to improve the production rates and lower the specific electrophoretic energy consumption values in preparative-scale, recirculating, binary isoelectric trapping separations, we propose to add an auxiliary isoelectric agent to the solution in the anodic separation compartment and another to the solution in the cathodic separation compartment to implement pH-biased isoelectric trapping. The auxiliary isoelectric agents are selected such that they are trapped in the respective anodic and cathodic separation compartments and also, have isoelectric point (pI) values that are different from the pI values of the analytes of interest. By proper selection of the auxiliary isoelectric agents and their concentrations, the analytes of interest can be kept in nonisoelectric, charged state during the entire course of the preparative-scale, recirculating, binary isoelectric trapping separation. This results in higher electrophoretic mobilities and solubilities for the analytes than in their isoelectric or near-isoelectric states, and leads to faster binary isoelectric trapping separations.

摘要

为了提高制备规模的循环二元等电聚焦捕集分离的产率并降低比电泳能耗值,我们建议在阳极分离室的溶液中添加一种辅助等电试剂,在阴极分离室的溶液中添加另一种辅助等电试剂,以实现pH偏倚等电聚焦捕集。选择辅助等电试剂时,要使其被困在各自的阳极和阴极分离室中,并且其等电点(pI)值与目标分析物的pI值不同。通过适当选择辅助等电试剂及其浓度,在制备规模的循环二元等电聚焦捕集分离的整个过程中,目标分析物可以保持在非等电的带电状态。这使得分析物的电泳迁移率和溶解度高于其等电或近等电状态,从而实现更快的二元等电聚焦捕集分离。

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