Membrane-based nanoscale proteolytic reactor enabling protein digestion, peptide separation, and protein identification using mass spectrometry

被引:113
作者
Cooper, JW [1 ]
Chen, JZ [1 ]
Li, Y [1 ]
Lee, CS [1 ]
机构
[1] Univ Maryland, Dept Chem & Biochem, College Pk, MD 20742 USA
关键词
D O I
10.1021/ac025768b
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A miniaturized trypsin membrane reactor housed inside a commonly used capillary fitting is developed and demonstrated for enabling rapid and sensitive protein identification by on-line proteolytic digestion and analysis of protein digests using nano-ESI-MS and MALDI-MS. The design and assembly of the capillary fitting-based trypsin membrane reactor are straightforward and highly robust, without the need for expensive fabrication technology and procedures. The resultant protein digests can also be further concentrated and resolved using capillary reversed-phase liquid chromatography or transient capillary isotachophoresis/zone electrophoresis prior to the mass spectrometric analysis in an integrated platform. By comparing these results with the results obtained from our previous studies using plastic microfluidics (Gao et al., AnaL Chem. 2001, 73, 2648-2655), significant reduction in dead volume and sample consumption can be achieved using this newly developed tryptic digestion station. This nanoscale reaction system enables rapid proteolytic digestion in seconds instead of hours for a protein concentration of less than 10(-8) M, consumes very little sample (less than or equal to 5 fmol), and offers capillary interfaces with various separation and mass spectrometry techniques. The ultrafast enzymatic turnover for attaining complete peptide coverage in protein identification is contributed by the highly porous structure of the membrane media, providing excessive trypsin loading while eliminating the constraints of diffusion-limited reaction kinetics.
引用
收藏
页码:1067 / 1074
页数:8
相关论文
共 38 条
[1]   Micro total analysis systems. 2. Analytical standard operations and applications [J].
Auroux, PA ;
Iossifidis, D ;
Reyes, DR ;
Manz, A .
ANALYTICAL CHEMISTRY, 2002, 74 (12) :2637-2652
[2]   A design for low-flow sheathless electrospray emitters [J].
Barnidge, DR ;
Nilsson, S ;
Markides, KE .
ANALYTICAL CHEMISTRY, 1999, 71 (19) :4115-4118
[3]   Influence of matrix solution conditions on the MALDI-MS analysis of peptides and proteins [J].
Cohen, SL ;
Chait, BT .
ANALYTICAL CHEMISTRY, 1996, 68 (01) :31-37
[4]   Utility of accurate mass tags for proteome-wide protein identification [J].
Conrads, TP ;
Anderson, GA ;
Veenstra, TD ;
Pasa-Tolic, L ;
Smith, RD .
ANALYTICAL CHEMISTRY, 2000, 72 (14) :3349-3354
[5]   RAPID TRYPTIC MAPPING USING ENZYMATICALLY ACTIVE MASS-SPECTROMETER PROBE TIPS [J].
DOGRUEL, D ;
WILLIAMS, P ;
NELSON, RW .
ANALYTICAL CHEMISTRY, 1995, 67 (23) :4343-4348
[6]   Integrated microanalytical technology enabling rapid and automated protein identification [J].
Ekström, S ;
Önnerfjord, P ;
Nilsson, J ;
Bengtsson, M ;
Laurell, T ;
Marko-Varga, G .
ANALYTICAL CHEMISTRY, 2000, 72 (02) :286-293
[7]  
ENJ JK, 1994, J AM SOC MASS SPECTR, V5, P976
[8]   TRACE ANALYSIS OF PROTEINS BY CAPILLARY ZONE ELECTROPHORESIS WITH ON-COLUMN TRANSIENT ISOTACHOPHORETIC PRECONCENTRATION [J].
FORET, F ;
SZOKO, E ;
KARGER, BL .
ELECTROPHORESIS, 1993, 14 (5-6) :417-428
[9]   Integrated microfluidic system enabling protein digestion, peptide separation, and protein identification [J].
Gao, J ;
Xu, JD ;
Locascio, LE ;
Lee, CS .
ANALYTICAL CHEMISTRY, 2001, 73 (11) :2648-2655
[10]   Rapid micro-scale proteolysis of proteins for MALDI-MS peptide mapping using immobilized trypsin [J].
Gobom, J ;
Nordhoff, E ;
Ekman, R ;
Roepstorff, P .
INTERNATIONAL JOURNAL OF MASS SPECTROMETRY, 1997, 169 :153-163