An Automated Cell-Free Workflow for Transcription Factor Engineering

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 μM Hg and 0, 1, 10, 100 μM 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.

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Publication Details

Journal
ACS Synthetic Biology
Published
2024-10-07
DOI
https://doi.org/10.1021/acssynbio.4c00471
Citations
20
Primary Topic
RNA and protein synthesis mechanisms
Type
article
Field-Weighted Citation Impact
4.68

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article

An Automated Cell-Free Workflow for Transcription Factor Engineering

Adam D. Silverman, Julius B. Lucks, Brenda Wang, Michael C. Jewett et al.
20 citations
ACS Synthetic Biology
RNA and protein synthesis mechanisms
4.68
article

An Automated Cell-Free Workflow for Transcription Factor Engineering

Adam D. Silverman, Julius B. Lucks, Brenda Wang, Michael C. Jewett, Ashty S. Karim, Holly M. Ekas
article en
20 citations

Abstract

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 μM Hg and 0, 1, 10, 100 μM 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.

ACS Synthetic BiologyVol. 13(10)
Northwestern University (US), IPM Institute of North America (US), Stanford University (US)
Bill and Melinda Gates Foundation, Paul and Daisy Soros Fellowships for New Americans, Northwestern University, National Defense Science and Engineering Graduate, Chemistry of Life Processes Institute, Air Force Office of Scientific Research, Army Research Office, Army Research Laboratory
Openalex Percentile: Top 4%
RNA and protein synthesis mechanisms
4.68
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