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
相关论文
共 50 条
  • [1] Towards On-Demand E. coli-Based Cell-Free Protein Synthesis of Tissue Plasminogen Activator
    Yang, Seung-Ook
    Nielsen, Gregory H.
    Wilding, Kristen M.
    Cooper, Merideth A.
    Wood, David W.
    Bundy, Bradley C.
    METHODS AND PROTOCOLS, 2019, 2 (02) : 1 - 8
  • [2] Methods to reduce variability in E. Coli-based cell-free protein expression experiments
    Dopp, Jared L.
    Jo, Yeong Ran
    Reuel, Nigel F.
    SYNTHETIC AND SYSTEMS BIOTECHNOLOGY, 2019, 4 (04) : 204 - 211
  • [3] A rational approach to improving titer inEscherichia coli-based cell-free protein synthesis reactions
    Colant, Noelle
    Melinek, Beatrice
    Teneb, Jaime
    Goldrick, Stephen
    Rosenberg, William
    Frank, Stefanie
    Bracewell, Daniel G.
    BIOTECHNOLOGY PROGRESS, 2021, 37 (01)
  • [4] Simplifying and streamlining Escherichia coli-based cell-free protein synthesis
    Yang, William C.
    Patel, Kedar G.
    Wong, H. Edward
    Swartz, James R.
    BIOTECHNOLOGY PROGRESS, 2012, 28 (02) : 413 - 420
  • [5] Rapid sensing of clinically relevant glutamine concentrations in human serum with metabolically engineered E. coli-based cell-free protein synthesis
    Hunt, J. Porter
    Barnett, R. Jordan
    Robinson, Hannah
    Soltani, Mehran
    Nelson, J. Andrew D.
    Bundy, Bradley C.
    JOURNAL OF BIOTECHNOLOGY, 2021, 325 : 389 - 394
  • [6] Sequence Specific Modeling of E. coli Cell-Free Protein Synthesis
    Vilkhovoy, Michael
    Horvath, Nicholas
    Shih, Che-Hsiao
    Wayman, Joseph A.
    Calhoun, Kara
    Swartz, James
    Varner, Jeffrey D.
    ACS SYNTHETIC BIOLOGY, 2018, 7 (08): : 1844 - 1857
  • [7] Development of a robust Escherichia coli-based cell-free protein synthesis application platform
    Jiang, Nan
    Ding, Xuanwei
    Lu, Yuan
    BIOCHEMICAL ENGINEERING JOURNAL, 2021, 165
  • [8] Using E. coli-based cell-free protein synthesis to evaluate the kinetic performance of an orthogonal tRNA and aminoacyl-tRNA synthetase pair
    Albayrak, Cem
    Swartz, James R.
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2013, 431 (02) : 291 - 295
  • [9] The Cost-Efficiency Realization in the Escherichia coli-Based Cell-Free Protein Synthesis Systems
    Lian, Qianqian
    Cao, Hongzhi
    Wang, Fengshan
    APPLIED BIOCHEMISTRY AND BIOTECHNOLOGY, 2014, 174 (07) : 2351 - 2367