Capacitively coupled contactless conductivity detection for microfluidic capillary isoelectric focusing

被引:12
|
作者
Chau, Minh Khang [1 ]
Arega, Nebiyu Getachew [1 ]
Nguyen Anh Nhung Tran [2 ]
Song, Jin [1 ]
Lee, Sangmin [2 ]
Kim, Jintae [3 ]
Chung, Minsub [2 ]
Kim, Dohyun [1 ,4 ]
机构
[1] Myongji Univ, Dept Mech Engn, Yongin 17508, Gyeonggi Do, South Korea
[2] Hongik Univ, Dept Chem Engn, Seoul 04066, South Korea
[3] Konkuk Univ, Dept Elect Engn, Seoul 05029, South Korea
[4] Myongji Univ, Nat Sci Res Inst, Yongin 17508, Gyeonggi Do, South Korea
基金
新加坡国家研究基金会;
关键词
Microfluidic isoelectric focusing; Protein analysis; Protein separation; Capacitively coupled contactless conductivity detection; Label-free detection; Numerical simulation; CARRIER AMPHOLYTES; PROTEIN SEPARATION; IMAGING-SYSTEM; ELECTROPHORESIS; MICROCHIP; CHIP; INTEGRATION; MOBILIZATION; PERFORMANCE; MICROSCOPY;
D O I
10.1016/j.aca.2020.05.028
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
We report capacitively coupled contactless conductivity detection (C4D) of proteins separated by microfluidic capillary isoelectric focusing (mu CIEF). To elucidate the evolution of negative conductivity peaks during focusing and seek IEF conditions for sensitive conductivity detection, numerical simulation was performed using a model protein GFP (green fluorescence protein) and hypothetical carrier ampholytes (CAs). C4D was successfully applied to the mu CIEF by optimizing assay conditions using a simple and effective pressure-mobilization approach. The conductivity and fluorescence signals of a focused GFP band were co-detected, confirming that the obtained negative C4D peak could be attributed to the actual protein, not the non-uniform background conductivity profile of the focused CAs. GFP concentrations of 10 nM-30 mu M was quantified with a detection limit of 10 nM. Finally, the resolving power was analyzed by separating a mixture of R-phycoerythrin (pI 5.01), GFP-F64L (pI 5.48), and RK-GFP (pI 6.02). The conductivities of the three separated fluorescence proteins were measured with average separation resolution of 2.06. We expect the newly developed label-free mu CIEF-C4D technique to be widely adopted as a portable, electronics-only protein-analysis tool. (C) 2020 Elsevier B.V. All rights reserved.
引用
收藏
页码:60 / 70
页数:11
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