Characterizing and prototyping genetic networks with cell-free transcription-translation reactions

被引:87
作者
Takahashi, Melissa K. [1 ]
Hayes, Clarmyra A. [2 ]
Chappell, James [1 ]
Sun, Zachary Z. [2 ]
Murray, Richard M. [2 ]
Noireaux, Vincent [3 ]
Lucks, Julius B. [1 ]
机构
[1] Cornell Univ, Sch Chem & Biomol Engn, Ithaca, NY 14850 USA
[2] CALTECH, Div Biol & Biol Engn, Pasadena, CA 91125 USA
[3] Univ Minnesota, Sch Phys & Astron, Minneapolis, MN 55455 USA
基金
美国国家科学基金会;
关键词
Cell-free systems; Transcription-translation (TX-TL); Rapid prototyping; Genetic networks; Synthetic biology; FREE PROTEIN-SYNTHESIS; SYNTHETIC BIOLOGY; ESCHERICHIA-COLI; IN-VITRO; FREE EXPRESSION; DESIGN; CIRCUIT; SYSTEM; ATP; CONSTRUCTION;
D O I
10.1016/j.ymeth.2015.05.020
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A central goal of synthetic biology is to engineer cellular behavior by engineering synthetic gene networks for a variety of biotechnology and medical applications. The process of engineering gene networks often involves an iterative 'design-build-test' cycle, whereby the parts and connections that make up the network are built, characterized and varied until the desired network function is reached. Many advances have been made in the design and build portions of this cycle. However, the slow process of in vivo characterization of network function often limits the timescale of the testing step. Cell-free transcription-t ranslation (TX-TL) systems offer a simple and fast alternative to performing these characterizations in cells. Here we provide an overview of a cell-free TX-TL system that utilizes the native Escherichia coli TX-TL machinery, thereby allowing a large repertoire of parts and networks to be characterized. As a way to demonstrate the utility of cell-free TX-TL, we illustrate the characterization of two genetic networks: an RNA transcriptional cascade and a protein regulated incoherent feed-forward loop. We also provide guidelines for designing TX-TL experiments to characterize new genetic networks. We end with a discussion of current and emerging applications of cell free systems. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:60 / 72
页数:13
相关论文
共 100 条
[1]   Cell-free synthesis of recombinant proteins from PCR-amplified genes at a comparable productivity to that of plasmid-based reactions [J].
Ahn, JH ;
Chu, HS ;
Kim, TW ;
Oh, IS ;
Choi, CY ;
Hahn, GH ;
Park, CG ;
Kim, DM .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2005, 338 (03) :1346-1352
[2]  
Algar R., 2013, Modelling the burden caused by gene expression: an in silico investigation into the interactions between synthetic gene circuits and their chassis cell
[3]  
Alon U., 2007, INTRO SYSTEMS BIOL D
[4]  
Anderson J.Christopher., 2006, Anderson promoter library registry of standard biological parts
[5]  
Appleton E, 2014, NAT METHODS, V11, P657, DOI [10.1038/NMETH.2939, 10.1038/nmeth.2939]
[6]   SECONDARY SIGMA-FACTOR CONTROLS TRANSCRIPTION OF FLAGELLAR AND CHEMOTAXIS GENES IN ESCHERICHIA-COLI [J].
ARNOSTI, DN ;
CHAMBERLIN, MJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (03) :830-834
[7]   Antisense RNA-mediated transcriptional attenuation:: an in vitro study of plasmid pT181 [J].
Brantl, S ;
Wagner, EGH .
MOLECULAR MICROBIOLOGY, 2000, 35 (06) :1469-1482
[8]   Optimization of a blueprint for in vitro glycolysis by metabolic real-time analysis [J].
Bujara, Matthias ;
Schuemperli, Michael ;
Pellaux, Rene ;
Heinemann, Matthias ;
Panke, Sven .
NATURE CHEMICAL BIOLOGY, 2011, 7 (05) :271-277
[9]   Site-Specific Incorporation of p-Propargyloxyphenylalanine in a Cell-Free Environment for Direct Protein-Protein Click Conjugation [J].
Bundy, Bradley C. ;
Swartz, James R. .
BIOCONJUGATE CHEMISTRY, 2010, 21 (02) :255-263
[10]   A brief history of synthetic biology [J].
Cameron, D. Ewen ;
Bashor, Caleb J. ;
Collins, James J. .
NATURE REVIEWS MICROBIOLOGY, 2014, 12 (05) :381-390