Automated design of synthetic ribosome binding sites to control protein expression

被引:1353
作者
Salis, Howard M. [1 ]
Mirsky, Ethan A. [2 ]
Voigt, Christopher A. [1 ]
机构
[1] Univ Calif San Francisco, Dept Pharmaceut Chem, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Grad Grp Biophys, San Francisco, CA 94143 USA
基金
美国国家卫生研究院;
关键词
ESCHERICHIA-COLI; THERMODYNAMIC PARAMETERS; TRANSLATIONAL EFFICIENCY; SECONDARY STRUCTURE; GENE NETWORKS; RNA; SEQUENCE; INITIATION; MODEL; MISMATCHES;
D O I
10.1038/nbt.1568
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
Microbial engineering often requires fine control over protein expression-for example, to connect genetic circuits(1-7) or control flux through a metabolic pathway(8-13). To circumvent the need for trial and error optimization, we developed a predictive method for designing synthetic ribosome binding sites, enabling a rational control over the protein expression level. Experimental validation of >100 predictions in Escherichia coli showed that the method is accurate to within a factor of 2.3 over a range of 100,000-fold. The design method also correctly predicted that reusing identical ribosome binding site sequences in different genetic contexts can result in different protein expression levels. We demonstrate the method's utility by rationally optimizing protein expression to connect a genetic sensor to a synthetic circuit. The proposed forward engineering approach should accelerate the construction and systematic optimization of large genetic systems.
引用
收藏
页码:946 / U112
页数:7
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