Reassemblable quasi-chip free-flow electrophoresis with simple heating dispersion for rapid micropreparation of trypsin in crude porcine pancreatin

被引:8
作者
Geng, Jia-Zhen [1 ]
Shao, Jing [1 ]
Yang, Jing-Hua [1 ]
Pang, Bo [1 ]
Cao, Cheng-Xi [1 ]
Fan, Liu-Yin [1 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Life Sci & Biotechnol, Lab Analyt Biochem & Bioseparat, State Key Lab Microbial Metab, Shanghai 200240, Peoples R China
基金
中国国家自然科学基金;
关键词
Free-flow electrophoresis; Micropreparation; Micropurification; Porcine pancreatin; Trypsin; MASS-SPECTROMETRIC ANALYSIS; COLI CELL EXTRACT; ZONE ELECTROPHORESIS; GRATIS GRAVITY; ALCOHOL-DEHYDROGENASE; SAMPLE PREPARATION; YEAST EXTRACT; BAND-WIDTH; SCALE-UP; PURIFICATION;
D O I
10.1002/elps.201100358
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
An increasing number of small biosamples (e.g. proteins and enzymes) need micropreparation in lab. However, neither large-scale free-flow electrophoresis (LS-FFE) nor chip FFE (C-FFE) could fit the growing demands. Herein, a simple quasi-chip FFE (QC-FFE) was constructed. In contrast to C-FFE, the features of QC-FFE are as follows: (i) its separation chamber is reassemblable and rewashable avoiding discard of C-FFE due to blockage of solute precipitation in chamber; (ii) its chamber size is 45 mm x 30mm x (80500)mu m (108654 mu L volume) having function of micropreparation; (iii) there are up to 16 outlets in QC-FFE bestowing fine fraction for micropurification. The QC-FFE was used for the micropurification of model enzyme of self-digestible trypsin in crude pancreatin. Under the given conditions, the purification factor of enzyme was 11.7, the specific activity reached 6236 U/mg, the run time for 19 mu L sample purification was 45 s and the throughput of trypsin was 3.34 mg/h, and the yield of pure trypsin was 55.2%. All of the results show the feasibility of enzyme micropreparation via QC-FFE. The developed device and procedure have potential use to other micropurification of protein or peptide sample.
引用
收藏
页码:3248 / 3256
页数:9
相关论文
共 54 条
[31]   SEPARATION OF ENZYMES FROM CANDIDA-BOIDINII CRUDE EXTRACT BY CONTINUOUS-FLOW ZONE ELECTROPHORESIS [J].
NATH, S ;
SCHUTTE, H ;
WEBER, G ;
HUSTEDT, H ;
DECKWER, WD .
ELECTROPHORESIS, 1990, 11 (11) :937-941
[32]  
Nath S, 1996, BIOTECHNOL BIOENG, V51, P15, DOI 10.1002/(SICI)1097-0290(19960705)51:1<15::AID-BIT2>3.0.CO
[33]  
2-3
[34]  
Natsume T, 2002, PROTEOMICS, V2, P1247, DOI 10.1002/1615-9861(200209)2:9<1247::AID-PROT1247>3.0.CO
[35]  
2-V
[36]   Microseparation sciences: Perspectives and recent advances. With recognition of Shigeru Terabe - Foreword [J].
Otsuka, K ;
Baba, Y .
JOURNAL OF CHROMATOGRAPHY A, 2006, 1106 (1-2) :1-2
[37]   Continuous flow separations in microfluidic devices [J].
Pamme, Nicole .
LAB ON A CHIP, 2007, 7 (12) :1644-1659
[38]   Immobilized gallium(III) affinity chromatography of phosphopeptides [J].
Posewitz, MC ;
Tempst, P .
ANALYTICAL CHEMISTRY, 1999, 71 (14) :2883-2892
[39]   TRYPSIN PURIFICATION BY AFFINITY BINDING TO SMALL UNILAMELLAR LIPOSOMES [J].
POWERS, JD ;
KILPATRICK, PK ;
CARBONELL, RG .
BIOTECHNOLOGY AND BIOENGINEERING, 1990, 36 (05) :506-519
[40]   CONTINUOUS SAMPLE PRETREATMENT USING A FREE-FLOW ELECTROPHORESIS DEVICE INTEGRATED ONTO A SILICON CHIP [J].
RAYMOND, DE ;
MANZ, A ;
WIDMER, HM .
ANALYTICAL CHEMISTRY, 1994, 66 (18) :2858-2865