Integration of Protein Processing Steps on a Droplet Microfluidics Platform for MALDI-MS Analysis

被引:64
作者
Chatterjee, Debalina [1 ]
Ytterberg, A. Jimmy [1 ]
Son, Sang Uk [1 ]
Loo, Joseph A. [1 ,2 ]
Garrell, Robin L. [1 ,3 ]
机构
[1] Univ Calif Los Angeles, Dept Chem & Biochem, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Dept Biol Chem, Los Angeles, CA 90095 USA
[3] Univ Calif Los Angeles, Calif NanoSyst Inst, Los Angeles, CA 90095 USA
基金
美国国家卫生研究院;
关键词
ON-A-CHIP; MASS-SPECTROMETRY; DIGITAL MICROFLUIDICS; CAPILLARY-ELECTROPHORESIS; TOF ANALYSIS; PROTEOMICS; MICROCHIP; DIELECTROPHORESIS; TECHNOLOGIES; ADSORPTION;
D O I
10.1021/ac9029373
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A droplet-based (digital) microfluidics platform has been developed to prepare and purify protein samples for measurement by matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS). Liquid droplets are moved in air by sequentially applying an electric potential to an array of electrodes patterned beneath it hydrophobic dielectric layer. We show that a complete integrated sequence of protein processing steps can be performed on this platform, including disulfide reduction, alkylation, and enzymatic digestion, followed by cocrystallization with a MALDI matrix and analysis of the sample in situ by MALDI-MS. Proteins carbonic anhydrase, cytochrome c, and ubiquitin were used to demonstrate the digestion and postdigestion steps; insulin, serum albumin, and lysozyme were used to illustrate the complete sequence of protein processing steps available with the platform, Several functional improvements in the platforrn are reported, notably, the incorporation of acetonitrile in the protein droplets to facilitate movement, and patterning the device surfaces to optimize sample crystallization. The method is fast, simple, repeatable, and results in lower reagent consumption and sample loss than conventional techniques for proteomics sample preparation.
引用
收藏
页码:2095 / 2101
页数:7
相关论文
共 72 条
[51]   BIOLOGICAL-ACTIVITY OF UREASE FORMULATED IN POLOXAMER 407 AFTER INTRAPERITONEAL INJECTION IN THE RAT [J].
PEC, EA ;
WOUT, ZG ;
JOHNSTON, TP .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1992, 81 (07) :626-630
[52]  
Perkins DN, 1999, ELECTROPHORESIS, V20, P3551, DOI 10.1002/(SICI)1522-2683(19991201)20:18<3551::AID-ELPS3551>3.0.CO
[53]  
2-2
[54]   Enzymatic microreactor-on-a-chip:: Protein mapping using trypsin immobilized on porous polymer monoliths molded in channels of microfluidic devices [J].
Peterson, DS ;
Rohr, T ;
Svec, F ;
Fréchet, JMJ .
ANALYTICAL CHEMISTRY, 2002, 74 (16) :4081-4088
[55]   Electrowetting-based actuation of liquid droplets for microfluidic applications [J].
Pollack, MG ;
Fair, RB ;
Shenderov, AD .
APPLIED PHYSICS LETTERS, 2000, 77 (11) :1725-1726
[56]   Influence of the electrical double layer in electrowetting [J].
Quinn, A ;
Sedev, R ;
Ralston, J .
JOURNAL OF PHYSICAL CHEMISTRY B, 2003, 107 (05) :1163-1169
[57]   High-efficiency, two-dimensional separations of protein digests on microfluidic devices [J].
Ramsey, JD ;
Jacobson, SC ;
Culbertson, CT ;
Ramsey, JM .
ANALYTICAL CHEMISTRY, 2003, 75 (15) :3758-3764
[58]  
Ro KW, 2002, ELECTROPHORESIS, V23, P1129, DOI 10.1002/1522-2683(200204)23:7/8<1129::AID-ELPS1129>3.0.CO
[59]  
2-4
[60]   Cell lysis and protein extraction in a microfluidic device with detection by a fluorogenic enzyme assay [J].
Schilling, EA ;
Kamholz, AE ;
Yager, P .
ANALYTICAL CHEMISTRY, 2002, 74 (08) :1798-1804