On-chip single column transient isotachophoresis with free zone electrophoresis for preconcentration and separation of α-lactalbumin and β-lactoglobulin

被引:10
|
作者
Crevillen, Agustin G. [1 ,2 ]
de Frutos, Mercedes [1 ]
Diez-Masa, Jose Carlos [1 ,2 ]
机构
[1] Inst Organ Chem IQOG CSIC, Madrid, Spain
[2] UNED, Fac Sci, Dept Analyt Sci, Senda Rey 9, E-28040 Madrid, Spain
关键词
ITP; Preconcentration; Microchip electrophoresis; Protein; Fluorescence detection; Zone electrophoresis; ELECTROKINETIC SUPERCHARGING PRECONCENTRATION; POLY(METHYL METHACRYLATE) MICROCHIP; LASER-INDUCED FLUORESCENCE; CAPILLARY-ELECTROPHORESIS; WHEY PROTEINS; SAMPLE STACKING; GEL-ELECTROPHORESIS; SENSITIVITY; QUANTIFICATION; OPTIONS;
D O I
10.1016/j.microc.2017.04.040
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Isotachophoresis (ITP) coupled to zone electrophoresis (ZE), either free zone electrophoresis (FZE) or gel electrophoresis (GE), carried out mainly in capillaries and, although less frequently, also in microchips, is a powerful preconcentration and separation technique which has been successfully used for the study of many low molecular-weight analytes. However, this analytical technique has been scarcely applied for proteins separation. In this work, an on-chip transient ITP coupled to free zone electrophoresis (t-ITP-MFZE) mode with LIF detection is developed for the preconcentration and separation of the proteins a-lactalbumin and beta-lactoglobulin. Firstly, for LIF detection, the proteins were off-chip fluorescently labeled with the fluorogenic reagent Chromeo P503. Then, several separation parameters in t-ITP-MFZE mode such as leading electrolyte, terminating electrolyte, separation voltage, and injection time were optimized to achieve the maximum sensitivity while maintaining an adequate resolution between a-lactalbumin and beta-lactoglobulin in a single column configuration t-ITP. Using the optimized electrolytes (50 mM imidazole/HCI pH = 8 as leading electrolyte and 100 mM imidazole/12 mM HEPES pH = 8 as terminating electrolyte) separation of both proteins was achieved in less than 4 min with peak resolution of 1.5. The LODs were 55 nM and 380 nM, for a-lactalbumin and beta-lactoglobulin, respectively, which are adequate for some food allergenicity studies. Finally, comparison of the optimized t-ITP-MFZE method to the equivalent MFZE method, carried out also in microchips but without the isotachophoretic preconceritration step, provided preconcentration indexes for both proteins around 10. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:600 / 606
页数:7
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