An Automated Cell-Free Workflow for Transcription Factor Engineering

被引:5
作者
Ekas, Holly M. [1 ,2 ,3 ]
Wang, Brenda [1 ,2 ,3 ]
Silverman, Adam D. [1 ,2 ,3 ]
Lucks, Julius B. [1 ,2 ,3 ,4 ]
Karim, Ashty S. [1 ,2 ,3 ]
Jewett, Michael C. [1 ,2 ,3 ,5 ,6 ,7 ]
机构
[1] Northwestern Univ, Dept Chem & Biol Engn, Evanston, IL 60208 USA
[2] Northwestern Univ, Chem Life Proc Inst, Evanston, IL 60208 USA
[3] Northwestern Univ, Ctr Synthet Biol, Evanston, IL 60208 USA
[4] Northwestern Univ, Ctr Engn Sustainabil & Resilience, Evanston, IL 60208 USA
[5] Northwestern Univ, Robert H Lurie Comprehens Canc Ctr, Chicago, IL 60611 USA
[6] Northwestern Univ, Simpson Querrey Inst, Chicago, IL 60611 USA
[7] Stanford Univ, Dept Bioengn, Stanford, CA 94305 USA
来源
ACS SYNTHETIC BIOLOGY | 2024年 / 13卷 / 10期
关键词
cell-free gene expression; synthetic biology; transcription factor; high-throughput; roboticliquid handling; protein engineering; MUTANTS IMPLICATE; PROTEIN; MERR; REPRESSION; ACTIVATION;
D O I
10.1021/acssynbio.4c00471
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The design and optimization of metabolic pathways, genetic systems, and engineered proteins rely on high-throughput assays to streamline design-build-test-learn cycles. However, assay development is a time-consuming and laborious process. Here, we create a generalizable approach for the tailored optimization of automated cell-free gene expression (CFE)-based workflows, which offers distinct advantages over in vivo assays in reaction flexibility, control, and time to data. Centered around designing highly accurate and precise transfers on the Echo Acoustic Liquid Handler, we introduce pilot assays and validation strategies for each stage of protocol development. We then demonstrate the efficacy of our platform by engineering transcription factor-based biosensors. As a model, we rapidly generate and assay libraries of 127 MerR and 134 CadR transcription factor variants in 3682 unique CFE reactions in less than 48 h to improve limit of detection, selectivity, and dynamic range for mercury and cadmium detection. This was achieved by assessing a panel of ligand conditions for sensitivity (to 0.1, 1, 10 mu M Hg and 0, 1, 10, 100 mu M Cd for MerR and CadR, respectively) and selectivity (against Ag, As, Cd, Co, Cu, Hg, Ni, Pb, and Zn). We anticipate that our Echo-based, cell-free approach can be used to accelerate multiple design workflows in synthetic biology.
引用
收藏
页码:3389 / 3399
页数:11
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