A bilayer cell-free protein synthesis system for high-throughput screening of gene products

被引:173
|
作者
Sawasaki, T
Hasegawa, Y
Tsuchimochi, M
Kamura, N
Ogasawara, T
Kuroita, T
Endo, Y [1 ]
机构
[1] Ehime Univ, Venture Business Lab, Fac Engn, Dept Appl Chem, Matsuyama, Ehime 7908577, Japan
[2] Toyobo Co Ltd, Tsuruga Inst Biotechnol, Tsuruga 9140047, Japan
关键词
cell-free protein synthesis; bilayer reaction method; Escherichia coli coupled transcription-translation; wheat germ system; high-throughput screening;
D O I
10.1016/S0014-5793(02)02329-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A high-throughput cell-free protein synthesis method has been described. The methodology is based on a bilayer diffusion system that enables the continuous supply of substrates, together with the continuous removal of small byproducts, through a phase between the translation mixture and substrate mixture. With the use of a multititer plate the system was functional for a prolonged time, and as a consequence yielded more than 10 times that of the similar batch-mode reaction. Combining this method with a wheat germ cell-free translation system developed by us, the system could produce a large amount of protein sufficient for carrying out functional analyses. This novel bilayer-based cell-free protein synthesis system with its simplicity, minimum time and low cost may be useful practical methodology in the post-genome era. (C) 2002 Federation of European Biochemical Societies. Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:102 / 105
页数:4
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