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通过部分刻蚀多孔界面将基于整体固定化 pH 梯度的毛细管等电聚焦和毛细管区带电泳在线组合用于蛋白质分析。

On-line combination of monolithic immobilized pH gradient-based capillary isoelectric focusing and capillary zone electrophoresis via a partially etched porous interface for protein analysis.

机构信息

Key Laboratory of Separation Science for Analytical Chemistry, National Chromatographic Research and Analysis Center, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian, China.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2011 Apr 1;879(11-12):804-10. doi: 10.1016/j.jchromb.2011.02.020. Epub 2011 Feb 21.

Abstract

An integrated platform consisting of monolithic immobilized pH gradient-based capillary isoelectric focusing (M-IPG CIEF) and capillary zone electrophoresis (CZE) coupled by a partially etched porous interface was established. Since carrier ampholytes (CAs) were immobilized on monolith in M-IPG CIEF to form a stable pH gradient, subsequent depletion of CAs at the interface to prevent the interference on CZE separation and detection were avoided. Moreover, a partially etched porous capillary column, which was facile for fabrication and durable for operation, was exploited as the interface to combine M-IPG CIEF and CZE. The RSD values in terms of the migration time for M-IPG CIEF separation, transfer protein from the first dimension to the second dimension, and CZE separation, were 2.4%, 3.9% and 2.3%, respectively. With a 6-protein mixture as the sample, two-dimensional capillary electrophoresis (2D-CE) separation was successfully completed within 116 min, yielding a peak capacity of ∼200 even with minute sample amount down to 5.0 μg/mL. The limit of detection was 0.2 μg/mL. In addition, proteins extracted from milk were used to test the performance of such a 2D-CE separation platform. We expect that such a novel 2D-CE system would provide a promising tool for protein separation with high throughput and high peak capacity.

摘要

建立了由整体固定化 pH 梯度毛细管等电聚焦(M-IPG CIEF)和毛细管区带电泳(CZE)组成的集成平台,通过部分刻蚀的多孔界面进行偶联。由于在 M-IPG CIEF 中载体两性电解质(CA)被固定在整体上以形成稳定的 pH 梯度,因此避免了在界面处 CA 的耗尽,以防止对 CZE 分离和检测的干扰。此外,还利用易于制造且操作耐用的部分刻蚀多孔毛细管柱作为界面,将 M-IPG CIEF 和 CZE 结合在一起。M-IPG CIEF 分离、将蛋白质从第一维转移到第二维以及 CZE 分离的迁移时间的 RSD 值分别为 2.4%、3.9%和 2.3%。使用 6 种蛋白质混合物作为样品,成功地在 116 分钟内完成了二维毛细管电泳(2D-CE)分离,即使样品量少至 5.0μg/mL,峰容量也约为 200。检测限为 0.2μg/mL。此外,还使用从牛奶中提取的蛋白质来测试这种 2D-CE 分离平台的性能。我们期望这种新型的 2D-CE 系统将为具有高通量和高峰容量的蛋白质分离提供一种有前途的工具。

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