Cloning technologies for protein expression and purification

被引:55
作者
Hartley, James L. [1 ]
机构
[1] NCI, SAIC Frederick Inc, Prot Express Lab, Res Technol Program, Ft Detrick, MD 21702 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1016/j.copbio.2006.06.011
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Detailed knowledge of the biochemistry and structure of individual proteins is fundamental to biomedical research. To further our understanding, however, proteins need to be purified in sufficient quantities, usually from recombinant sources. Although the sequences of genomes are now produced in automated factories purified proteins are not, because their behavior is much more variable. The construction of plasmids and viruses to overexpress proteins for their purification is often tedious. Alternatives to traditional methods that are faster, easier and more flexible are needed and are becoming available.
引用
收藏
页码:359 / 366
页数:8
相关论文
共 47 条
[1]   High throughput cloning and expression strategies for protein production [J].
Betton, JM .
BIOCHIMIE, 2004, 86 (9-10) :601-605
[2]   High efficiency single step production of expression plasmids from cDNA clones using the Flexi Vector cloning system [J].
Blommel, Paul G. ;
Martin, Peter A. ;
Wrobel, Russell L. ;
Steffen, Eric ;
Fox, Brian G. .
PROTEIN EXPRESSION AND PURIFICATION, 2006, 47 (02) :562-570
[3]  
Cabantous Stephanie, 2005, Journal of Structural and Functional Genomics, V6, P113, DOI 10.1007/s10969-005-5247-5
[4]   A family of E-coli expression vectors for laboratory scale and high throughput soluble protein production [J].
Cabrita, LD ;
Dai, WW ;
Bottomley, SP .
BMC BIOTECHNOLOGY, 2006, 6 (1)
[5]  
CHANDA PK, 2005, IN PRESS PROTEIN EXP
[6]  
CHEESEMAN IM, 2005, SCI STKE, P1
[7]   Concerted assembly and cloning of multiple DNA segments using in vitro site-specific recombination: Functional analysis of multi-segment expression clones [J].
Cheo, DL ;
Titus, SA ;
Byrd, DRN ;
Hartley, JL ;
Temple, GF ;
Brasch, MA .
GENOME RESEARCH, 2004, 14 (10B) :2111-2120
[8]   Modification of the Creator recombination system for proteomics applications - improved expression by addition of splice sites [J].
Colwill, K ;
Wells, CD ;
Elder, K ;
Goudreault, M ;
Hersi, K ;
Kulkarni, S ;
Hardy, WR ;
Pawson, T ;
Morin, GB .
BMC BIOTECHNOLOGY, 2006, 6 (1)
[9]  
DONNELLY MI, 2006, IN PRESS PROTEIN EXP
[10]   Gateway cloning is compatible with protein secretion from Pichia pastoris [J].
Esposito, D ;
Gillette, WK ;
Miller, DA ;
Taylor, TE ;
Frank, PH ;
Hu, RQ ;
Bekisz, J ;
Hernandez, J ;
Cregg, JM ;
Zoon, KC ;
Hartley, JL .
PROTEIN EXPRESSION AND PURIFICATION, 2005, 40 (02) :424-428