Cell-Free Protein Synthesis as a Method to Rapidly Screen Machine Learning-Generated Protease Variants.

Journal: ACS synthetic biology
PMID:

Abstract

Machine learning (ML) tools have revolutionized protein structure prediction, engineering, and design, but the best ML tool is only as good as the training data it learns from. To obtain high-quality structural or functional data, protein purification is typically required, which is both time and resource consuming, especially at the scale required to train ML tools. Here, we showcase cell-free protein synthesis as a straightforward and fast tool for screening and scoring the activity of protein variants in ML workflows. We demonstrate the utility of the system by improving the kinetic qualities of a protease. By rapidly screening just 48 random variants to initially sample the fitness landscape, followed by 32 more targeted variants, we identified several protease variants with improved kinetic properties.

Authors

  • Ella Lucille Thornton
    Centre for Engineering Biology, Institute of Quantitative Biology, Biochemistry and Biotechnology, School of Biological Sciences, University of Edinburgh, Edinburgh EH9 3BF, Scotland.
  • Jeremy T Boyle
    Centre for Engineering Biology, Institute of Quantitative Biology, Biochemistry and Biotechnology, School of Biological Sciences, University of Edinburgh, Edinburgh EH9 3BF, Scotland.
  • Nadanai Laohakunakorn
    School of Biological Sciences, University of Edinburgh, Roger Land Building, Alexander Crum Brown Road, The King's Buildings, Edinburgh, Scotland EH9 3FF, U.K.
  • Lynne Regan
    Centre for Engineering Biology, Institute of Quantitative Biology, Biochemistry and Biotechnology, School of Biological Sciences, University of Edinburgh, Edinburgh EH9 3BF, Scotland.