High-throughput cell-free systems for synthesis of functionally active proteins

被引:166
作者
Spirin, AS [1 ]
机构
[1] Russian Acad Sci, Inst Prot Res, Pushchino 142290, Moscow Region, Russia
关键词
D O I
10.1016/j.tibtech.2004.08.012
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Continuous cell-free translation systems with perpetual supply of consumable substrates and removal of reaction products made the process of in vitro synthesis of individual proteins sustainable and productive. Improvements of cell-free reaction mixtures, including new ways for efficient energy generation, had an additional impact on progress in cell-free protein synthesis technology. The requirement for gene-product identification in genomic studies, the development of high-throughput structural proteomics, the need for protein engineering without cell constraints (including the use of unnatural amino acids), and the need to produce cytotoxic, poorly expressed and unstable proteins have caused increased interest in cell-free protein synthesis technologies for molecular biologists, biotechnologists and pharmacologists.
引用
收藏
页码:538 / 545
页数:8
相关论文
共 78 条
[1]  
BARANOV VI, 1993, METHOD ENZYMOL, V217, P123
[2]   GENE-EXPRESSION IN A CELL-FREE SYSTEM ON THE PREPARATIVE SCALE [J].
BARANOV, VI ;
MOROZOV, IY ;
ORTLEPP, SA ;
SPIRIN, AS .
GENE, 1989, 84 (02) :463-466
[3]   Rapid translation system (RTS): A promising alternative for recombinant protein production [J].
Betton, JM .
CURRENT PROTEIN & PEPTIDE SCIENCE, 2003, 4 (01) :73-80
[4]  
BETTON JM, 2002, CELL FREE TRANSLATIO, P219
[5]  
BUCHBERGER B, 2002, CELL FREE TRANSLATIO, P121
[6]  
Budisa N, 2003, CELL-FREE PROTEIN EXPRESSION, P89
[7]  
Busso D, 2003, CELL-FREE PROTEIN EXPRESSION, P109
[8]   Expression of soluble recombinant proteins in a cell-free system using a 96-well format [J].
Busso, D ;
Kim, R ;
Kim, SH .
JOURNAL OF BIOCHEMICAL AND BIOPHYSICAL METHODS, 2003, 55 (03) :233-240
[9]  
CHO HS, 2002, CELL FREE TRANSLATIO, P227
[10]   DNA-DIRECTED PEPTIDE SYNTHESIS .2. SYNTHESIS OF ALPHA-FRAGMENT OF ENZYME BETA-GALACTOSIDASE [J].
DEVRIES, JK ;
ZUBAY, G .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1967, 57 (04) :1010-&