From DNA to protein: No living cells required

被引:13
作者
He, Mingyue [1 ]
He, Yongzhi [2 ]
Luo, Qin [3 ]
Wang, Mingrong [2 ]
机构
[1] Babraham Inst, Prot Express Facil, Cambridge CB22 3AT, England
[2] Sichuan Ind Inst Antibiot, Ctr Prot Engn, Chengdu, Sichuan, Peoples R China
[3] Sichuan Univ, Coll Life Sci, Chengdu, Sichuan, Peoples R China
关键词
Protein synthesis; Cell-free system; High-throughput methods; Cell-free protein technologies; VITRO TRANSLATION SYSTEM; IN-VITRO; ESCHERICHIA-COLI; FREE EXPRESSION; RIBOSOMAL SYNTHESIS; HIGHLY EFFICIENT; FUSION PROTEINS; WHEAT-GERM; AMINO-ACID; SELECTION;
D O I
10.1016/j.procbio.2010.11.003
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
Proteomics and biotechnology studies require simple and rapid methods to convert the genetic information into proteins. Whereas heterologous protein expression in living cells is a time-consuming process, in vitro translation directs protein synthesis in hours from added linear PCR DNA without the need for E. colt cloning, thus providing an attractive alternative to cell-based methods for high throughput production of proteins. Moreover, the open nature of cell-free systems and availability of various prokaryotic and eukaryotic cellular lysates offers a flexible choice of conditions for synthesis of folded proteins or production of "difficult" proteins that are not possible by in vivo systems. Finally, cell-free extracts express protein populations in a single reaction, allowing for the development of powerful proteomic tools. This article will review the recent advances in cell-free protein expression and its applications in biotechnology, proteomics and fundamental biological research. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:615 / 620
页数:6
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