Characterizing and Improving Reaction Times for E. coli-Based Cell-Free Protein Synthesis

被引:12
|
作者
Burrington, Logan R. [1 ,2 ]
Watts, Katharine R. [1 ,2 ]
Oza, Javin P. [1 ,2 ]
机构
[1] Calif Polytech State Univ San Luis Obispo, Chem & Biochem Dept, San Luis Obispo, CA 93407 USA
[2] Calif Polytech State Univ San Luis Obispo, Ctr Applicat Biotechnol, San Luis Obispo, CA 93407 USA
来源
ACS SYNTHETIC BIOLOGY | 2021年 / 10卷 / 08期
基金
美国国家科学基金会;
关键词
cell-free protein synthesis; in vitro transcription/translation; synthetic biology; rapid; rate; CFAI; LOW-COST; TRANSCRIPTION; TRANSLATION;
D O I
10.1021/acssynbio.1c00195
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Cell-free protein synthesis (CFPS) is a platform biotechnology that has enabled the on-demand synthesis of proteins for a variety of applications. Numerous advances have improved the productivity of the CFPS platform to result in high-yielding reactions; however, many applications remain limited due to long reaction times. To overcome this limitation, we first established the benchmarks reaction times for CFPS across in-house E. coli extracts and commercial kits. We then set out to fine-tune our in-house extract systems to improve reaction times. Through the optimization of reaction composition and titration of low-cost additives, we have identified formulations that reduce reaction times by 30-50% to obtain high protein titers for biomanufacturing applications, and reduce times by more than 50% to reach the sfGFP detection limit for applications in education and diagnostics. Under optimum conditions, we report the visible observation of sfGFP signal in less than 10 min. Altogether, these advances enhance the utility of CFPS as a rapid, user-defined platform.
引用
收藏
页码:1821 / 1829
页数:9
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