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
[1]   The Digital Revolution: A New Paradigm for Microfluidics [J].
Abdelgawad, Mohamed ;
Wheeler, Aaron R. .
ADVANCED MATERIALS, 2009, 21 (08) :920-925
[2]   Hybrid microfluidics: A digital-to-channel interface for in-line sample processing and chemical separations [J].
Abdelgawad, Mohamed ;
Watson, Michael W. L. ;
Wheeler, Aaron R. .
LAB ON A CHIP, 2009, 9 (08) :1046-1051
[3]   Mass spectrometry-based proteomics [J].
Aebersold, R ;
Mann, M .
NATURE, 2003, 422 (6928) :198-207
[4]   PREVENTION OF PROTEIN ADSORPTION AND PLATELET-ADHESION ON SURFACES BY PEO PPO PEO TRIBLOCK COPOLYMERS [J].
AMIJI, M ;
PARK, K .
BIOMATERIALS, 1992, 13 (10) :682-692
[5]   The estimation of pepsin, trypsin, papain, and cathepsin with hemoglobin [J].
Anson, ML .
JOURNAL OF GENERAL PHYSIOLOGY, 1938, 22 (01) :79-89
[6]   Microfluidic systems and proteomics:: Applications of the electrocapture technology to protein and peptide analysis [J].
Astorga-Wells, J ;
Vollmer, S ;
Bergman, T ;
Jörnvall, H .
ANALYTICAL BIOCHEMISTRY, 2005, 345 (01) :10-17
[7]   Digital microfluidics for cell-based assays [J].
Barbulovic-Nad, Irena ;
Yang, Hao ;
Park, Philip S. ;
Wheeler, Aaron R. .
LAB ON A CHIP, 2008, 8 (04) :519-526
[8]   SOLUBILIZATION OF BACTERIAL-MEMBRANE PROTEINS USING ALKYL GLUCOSIDES AND DIOCTANOYL PHOSPHATIDYLCHOLINE [J].
BARON, C ;
THOMPSON, TE .
BIOCHIMICA ET BIOPHYSICA ACTA, 1975, 382 (03) :276-285
[9]   Dipolar anions are not preferentially attracted to the oil/water interface [J].
Beattie, JK ;
Djerdjev, AM ;
Franks, GV ;
Warr, GG .
JOURNAL OF PHYSICAL CHEMISTRY B, 2005, 109 (33) :15675-15676
[10]   Self-pinning protein-laden drops [J].
Berejnov, Viatcheslav V. .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 2008, 322 (01) :246-251