The Spinach RNA Aptamer as a Characterization Tool for Synthetic Biology

被引:78
作者
Pothoulakis, Georgios [1 ,2 ]
Ceroni, Francesca [1 ,2 ]
Reeve, Benjamin [1 ,2 ]
Ellis, Tom [1 ,2 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Ctr Synthet Biol & Innovat, London SW7 2AZ, England
[2] Univ London Imperial Coll Sci Technol & Med, Dept Bioengn, London SW7 2AZ, England
基金
英国工程与自然科学研究理事会;
关键词
measurement; Spinach RNA; aptamer; promoter; ribosome binding site; fluorescence; FLUORESCENT PROTEIN; ESCHERICHIA-COLI; RIBOSOME; POLYMERASE; EXPRESSION; PROMOTERS;
D O I
10.1021/sb400089c
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Characterization of genetic control elements is essential for the predictable engineering of synthetic biology systems. The current standard for in vivo characterization of control elements is through the use of fluorescent reporter proteins such as green fluorescent protein (GFP). Gene expression, however, involves not only protein production but also the production of mRNA. Here, we present the use of the Spinach aptamer sequence, an RNA mimic of GFP, as a tool to characterize mRNA expression in Escherichia coli. We show how the aptamer can be incorporated into gene expression cassettes and how co-expressing it with a red fluorescent protein (mRFP1) allows, for the first time, simultaneous measurement of mRNA and protein levels from engineered constructs. Using flow cytometry, we apply this tool here to evaluate ribosome binding site sequences to highlight the differences in the temporal behavior of transcription and translation.
引用
收藏
页码:182 / 187
页数:6
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