Published April 24, 2025 | Version v1
Publication Open

GROQ-seq Platform Expansion: Design of growth-coupled measurements of Dihydrofolate Reductase in vivo Biochemistry

  • 1. ROR icon The University of Texas Southwestern Medical Center
  • 2. The Align Foundation
  • 1. ROR icon University of California, San Francisco
  • 2. ROR icon Cold Spring Harbor Laboratory
  • 3. ROR icon Wellcome Sanger Institute
  • 4. ROR icon University of Manchester
  • 5. Stanford University
  • 6. National Institute of Standards and Technology
  • 7. Columbia University
  • 8. ROR icon University of Colorado Boulder

Description

This proposal details the development of a high-throughput, growth-based assay for measuring enzyme kinetics of Escherichia coli dihydrofolate reductase (DHFR) in vivo using the GROQ-seq platform. By linking DHFR activity and abundance to growth through engineered gene circuits, the system enables inference of catalytic parameters—kcat, Km, and enzyme abundance—from growth rate data. It includes both abundance and function selection modules, using antibiotic resistance fusions and substrate titration strategies, respectively. This approach allows disambiguation of mutational effects on enzyme kinetics and stability, overcoming limitations of traditional fitness-based assays. The work captures data from single, double, and multimutant DHFR variants and provides a scalable framework for extending in vivo biochemistry to other essential, growth-linked enzymes.

This effort is a step toward comprehensive sequence–function mapping for enzymes, supporting applications in evolutionary biology, enzyme engineering, and disease variant interpretation.

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Related works

Cites
Publication: 10.7554/eLife.53476 (DOI)
Is supplement to
Publication: 10.5281/zenodo.12521640 (DOI)