Integrated sample preparation and MALDI mass spectrometry on a microfluidic compact disk

被引:103
作者
Gustafsson, M
Hirschberg, D
Palmberg, C
Jörnvall, H
Bergman, T [1 ]
机构
[1] Karolinska Inst, Dept Med Biochem & Biophys, SE-17177 Stockholm, Sweden
[2] Gyros AB, SE-75183 Uppsala, Sweden
关键词
D O I
10.1021/ac030194b
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
High-throughput microfluidic processing of protein digests integrated with matrix-assisted laser desorption/ionization (MALDI) mass spectrometry on a compact disk (CD) is described. Centrifugal force moves liquid through multiple microstructures, each containing a 10-nL reversed-phase chromatography column. The CD enables parallel preparation of 96 samples with volumes ranging from one to several microliters. The peptides in the digests are concentrated, desalted, and subsequently eluted from the columns directly into MALDI target areas (200 x 400 mum) on the CD using a solvent containing the MALDI matrix. After crystallization, the CD is inserted into the MALDI instrument for peptide mass fingerprinting and database identification at a routine sensitivity down to the 200-amol level. Detection of proteolytic peptides down to the 50-amol level is demonstrated. The success rate of the CD technology in protein identification is about twice that of the C(18)ZipTips and standard MALDI steel targets. The CDs are operated using robotics to transfer samples and reagents from microcontainers to the processing inlets on the disposable CD and spinning to control the movement of liquid through the microstructures.
引用
收藏
页码:345 / 350
页数:6
相关论文
共 21 条
[1]   Mass spectrometry-based proteomics [J].
Aebersold, R ;
Mann, M .
NATURE, 2003, 422 (6928) :198-207
[2]  
Appella E, 2000, EXS, V88, P1
[3]   A microfluidic electrocapture device in sample preparation for protein analysis by MALDI mass spectrometry [J].
Astorga-Wells, J ;
Jörnvall, H ;
Bergman, T .
ANALYTICAL CHEMISTRY, 2003, 75 (19) :5213-5219
[4]   MATRIX SAMPLE INTERACTIONS IN ULTRAVIOLET LASER-DESORPTION OF PROTEINS [J].
DOKTYCZ, SJ ;
SAVICKAS, PJ ;
KRUEGER, DA .
RAPID COMMUNICATIONS IN MASS SPECTROMETRY, 1991, 5 (04) :145-148
[5]  
Ekstrand G, 2000, MESA MG, P311
[6]   Evaluation of two-dimensional gel electrophoresis-based proteome analysis technology [J].
Gygi, SP ;
Corthals, GL ;
Zhang, Y ;
Rochon, Y ;
Aebersold, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (17) :9390-9395
[7]   What place for polyacrylamide in proteomics? [J].
Herbert, BR ;
Harry, JL ;
Packer, NH ;
Gooley, AA ;
Pedersen, SK ;
Williams, KL .
TRENDS IN BIOTECHNOLOGY, 2001, 19 (10) :S3-S9
[8]   Thr94 in bovine myelin basic protein is a second phosphorylation site for 42-kDa mitogen-activated protein kinase (ERK2) [J].
Hirschberg, D ;
Rådmark, O ;
Jörnvall, H ;
Bergman, T .
JOURNAL OF PROTEIN CHEMISTRY, 2003, 22 (02) :177-181
[9]  
Jolles P., 2000, PROTEOMICS FUNCTIONA
[10]   Phosphospecific proteolysis for mapping sites of protein phosphorylation [J].
Knight, ZA ;
Schilling, B ;
Row, RH ;
Kenski, DM ;
Gibson, BW ;
Shokat, KM .
NATURE BIOTECHNOLOGY, 2003, 21 (09) :1047-1054