Use of self assembled magnetic beads for on-chip protein digestion

被引:104
作者
Slovakova, M
Minc, N
Bilkova, Z
Smadja, C
Faigle, W
Fütterer, C
Taverna, M
Viovy, JL
机构
[1] Inst Curie, Lab Physicochim Curie, UMR 168, CNRS, F-75248 Paris, France
[2] Univ Pardubice, Dept Biol & Biochem Sci, Pardubice 53210, Czech Republic
[3] Univ Paris 12, Grp Chim Analyt Paris Sud, F-92296 Chatenay Malabry, France
[4] Inst Curie, Sect Rech, Lab Spectrometrie Massel Proteom, F-75248 Paris, France
[5] Inst Curie, Lab Physicochim Curie, UMR 168, CNRS,Sect Rech, F-75005 Paris, France
关键词
D O I
10.1039/b504861c
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The use of grafted trypsin magnetic beads in a microchip for performing protein digestion is described. The PDMS device uses strong magnets to create a magnetic field parallel to the flow with a strong gradient pointing through the center of the chip channel. This allows for the formation of a low-hydrodynamic resistance plug of magnetic trypsin beads that serves as a matrix for protein digestion. This device represents an inexpensive way of fabricating a multi open-tubular-like column with an appropriate pore size for proteins. Kinetics studies of the hydrolysis of a model peptide show a 100-fold increase in digestion speed obtained by the microsystem when compared to a batch wise system. This system also offers the great advantage of easy replacement, as the bead matrix is easily washed out and replaced. High performance and reproducibility for digesting recombinant human growth hormone are confirmed by analysing the digest products in both CE and MALDI-TOF MS. Similar sequence coverage (of about 44%) is obtained from MS analysis of products after 10 minutes on-chip and 4 h with soluble trypsin in bulk.
引用
收藏
页码:935 / 942
页数:8
相关论文
共 38 条
[21]   Integration of microfabricated devices to capillary electrophoresis-electrospray mass spectrometry using a low dead volume connection: Application to rapid analyses of proteolytic digests [J].
Li, JJ ;
Thibault, P ;
Bings, NH ;
Skinner, CD ;
Wang, C ;
Colyer, C ;
Harrison, J .
ANALYTICAL CHEMISTRY, 1999, 71 (15) :3036-3045
[22]   Quantitative microfluidic separation of DNA in self-assembled magnetic matrixes [J].
Minc, N ;
Fütterer, C ;
Dorfman, KD ;
Bancaud, A ;
Gosse, C ;
Goubault, C ;
Viovy, JL .
ANALYTICAL CHEMISTRY, 2004, 76 (13) :3770-3776
[23]   Applications of magnetic nanoparticles in biomedicine [J].
Pankhurst, QA ;
Connolly, J ;
Jones, SK ;
Dobson, J .
JOURNAL OF PHYSICS D-APPLIED PHYSICS, 2003, 36 (13) :R167-R181
[24]  
Perkins DN, 1999, ELECTROPHORESIS, V20, P3551, DOI 10.1002/(SICI)1522-2683(19991201)20:18<3551::AID-ELPS3551>3.0.CO
[25]  
2-2
[26]   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
[27]   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
[28]   Automated microanalysis using magnetic beads with commercial capillary electrophoretic instrumentation [J].
Rashkovetsky, LG ;
Lyubarskaya, YV ;
Foret, F ;
Hughes, DE ;
Karger, BL .
JOURNAL OF CHROMATOGRAPHY A, 1997, 781 (1-2) :197-204
[29]   Chip-based microsystems for genomic and proteomic analysis [J].
Sanders, GHW ;
Manz, A .
TRAC-TRENDS IN ANALYTICAL CHEMISTRY, 2000, 19 (06) :364-378
[30]  
SEGEL IH, 1975, ENZYME KINETICS, pCH2A