bioRxivBiochemistry
Access to unexplored regions of sequence space in directed enzyme evolution via insertion/deletion mutagenesis
S. Emond, M. Petek, E. Kay, B. Heames, S. Devenish, N. Tokuriki, F. Hollfelder
Abstract
Insertions and deletions (InDels) are frequently observed in natural protein evolution, yet their potential remains untapped in laboratory evolution. Here we introduce a transposon mutagenesis approach (TRIAD) to generate libraries of random variants with short in-frame InDels, and screen TRIAD libraries to evolve a promiscuous arylesterase activity in a phosphotriesterase. The evolution exhibits features that are distinct from previous point mutagenesis campaigns: while the average activity of TRIAD variants is more deleterious, a larger proportion has successfully adapted for the new activity, exhibiting different functional profiles: (i) both strong and weak trade-off in original vs promiscuous activity are observed; (ii) trade-off is more severe (10- to 20-fold increased kcat/KM in arylesterase with [~]100-fold decreases in the original phosphotriesterase activity) and (iii) improvements show up in kcat rather than KM, suggesting novel adaptive solution. These distinct features make TRIAD an alternative to widely used point mutagenesis, providing access to functional innovations and traversing unexplored fitness landscape regions.
- assay: proteomics
- research focus: protein folding & dynamics
- research focus: drug response / drug discovery
- approach: experimental assay
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Ultrahigh-throughput directed evolution of a metal-free α/β-hydrolase with a Cys-His-Asp triad into an efficient phosphotriesterase
D. Schnettler Fernandez, O. J. Klein, … F. Hollfelder·bioRxiv·Feb 14, 2022
- YeastIT: Reducing mutational bias for in vivo directed evolution using a novel yeast mutator strain based on dual adenine-/cytosine-targeting and error-prone DNA repair
Marta Napiorkowska, Katrin Fischer, … Florian Hollfelder·bioRxiv·Nov 20, 2023
- Origin Of Evolutionary Bifurcation In An Enzyme
C. M. Miton, E. C. Campbell, … N. Tokuriki·bioRxiv·Nov 25, 2023
- Mutations that improve the efficiency of a weak-link enzyme are rare compared to adaptive mutations elsewhere in the genome
A. B. Morgenthaler, W. R. Kinney, … S. D. Copley·bioRxiv·Apr 30, 2019
- Substrate-dependent epistasis probes active site intramolecular wiring
Karol Buda, Charlotte M. Miton, … Nobuhiko Tokuriki·bioRxiv·Jul 3, 2026
- A combinatorially complete epistatic fitness landscape in an enzyme active site
Kadina E. Johnston, Patrick J. Almhjell, … Frances H. Arnold·Proceedings of the National Academy of SciencesPeer-reviewed·Jul 29, 2024