Cargando…

Accessing unexplored regions of sequence space in directed enzyme evolution via insertion/deletion mutagenesis

Insertions and deletions (InDels) are frequently observed in natural protein evolution, yet their potential remains untapped in laboratory evolution. Here we introduce a transposon-based mutagenesis approach (TRIAD) to generate libraries of random variants with short in-frame InDels, and screen TRIA...

Descripción completa

Detalles Bibliográficos
Autores principales: Emond, Stephane, Petek, Maya, Kay, Emily J., Heames, Brennen, Devenish, Sean R. A., Tokuriki, Nobuhiko, Hollfelder, Florian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7351745/
https://www.ncbi.nlm.nih.gov/pubmed/32651386
http://dx.doi.org/10.1038/s41467-020-17061-3
_version_ 1783557504355008512
author Emond, Stephane
Petek, Maya
Kay, Emily J.
Heames, Brennen
Devenish, Sean R. A.
Tokuriki, Nobuhiko
Hollfelder, Florian
author_facet Emond, Stephane
Petek, Maya
Kay, Emily J.
Heames, Brennen
Devenish, Sean R. A.
Tokuriki, Nobuhiko
Hollfelder, Florian
author_sort Emond, Stephane
collection PubMed
description Insertions and deletions (InDels) are frequently observed in natural protein evolution, yet their potential remains untapped in laboratory evolution. Here we introduce a transposon-based 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 differ from previous point mutagenesis campaigns: while the average activity of TRIAD variants is more compromised, a larger proportion has successfully adapted for the activity. Different functional profiles emerge: (i) both strong and weak trade-off between activities are observed; (ii) trade-off is more severe (20- to 35-fold increased k(cat)/K(M) in arylesterase with 60-400-fold decreases in phosphotriesterase activity) and (iii) improvements are present in k(cat) rather than just in K(M), suggesting adaptive solutions. These distinct features make TRIAD an alternative to widely used point mutagenesis, accessing functional innovations and traversing unexplored fitness landscape regions.
format Online
Article
Text
id pubmed-7351745
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-73517452020-07-13 Accessing unexplored regions of sequence space in directed enzyme evolution via insertion/deletion mutagenesis Emond, Stephane Petek, Maya Kay, Emily J. Heames, Brennen Devenish, Sean R. A. Tokuriki, Nobuhiko Hollfelder, Florian Nat Commun Article Insertions and deletions (InDels) are frequently observed in natural protein evolution, yet their potential remains untapped in laboratory evolution. Here we introduce a transposon-based 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 differ from previous point mutagenesis campaigns: while the average activity of TRIAD variants is more compromised, a larger proportion has successfully adapted for the activity. Different functional profiles emerge: (i) both strong and weak trade-off between activities are observed; (ii) trade-off is more severe (20- to 35-fold increased k(cat)/K(M) in arylesterase with 60-400-fold decreases in phosphotriesterase activity) and (iii) improvements are present in k(cat) rather than just in K(M), suggesting adaptive solutions. These distinct features make TRIAD an alternative to widely used point mutagenesis, accessing functional innovations and traversing unexplored fitness landscape regions. Nature Publishing Group UK 2020-07-10 /pmc/articles/PMC7351745/ /pubmed/32651386 http://dx.doi.org/10.1038/s41467-020-17061-3 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Emond, Stephane
Petek, Maya
Kay, Emily J.
Heames, Brennen
Devenish, Sean R. A.
Tokuriki, Nobuhiko
Hollfelder, Florian
Accessing unexplored regions of sequence space in directed enzyme evolution via insertion/deletion mutagenesis
title Accessing unexplored regions of sequence space in directed enzyme evolution via insertion/deletion mutagenesis
title_full Accessing unexplored regions of sequence space in directed enzyme evolution via insertion/deletion mutagenesis
title_fullStr Accessing unexplored regions of sequence space in directed enzyme evolution via insertion/deletion mutagenesis
title_full_unstemmed Accessing unexplored regions of sequence space in directed enzyme evolution via insertion/deletion mutagenesis
title_short Accessing unexplored regions of sequence space in directed enzyme evolution via insertion/deletion mutagenesis
title_sort accessing unexplored regions of sequence space in directed enzyme evolution via insertion/deletion mutagenesis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7351745/
https://www.ncbi.nlm.nih.gov/pubmed/32651386
http://dx.doi.org/10.1038/s41467-020-17061-3
work_keys_str_mv AT emondstephane accessingunexploredregionsofsequencespaceindirectedenzymeevolutionviainsertiondeletionmutagenesis
AT petekmaya accessingunexploredregionsofsequencespaceindirectedenzymeevolutionviainsertiondeletionmutagenesis
AT kayemilyj accessingunexploredregionsofsequencespaceindirectedenzymeevolutionviainsertiondeletionmutagenesis
AT heamesbrennen accessingunexploredregionsofsequencespaceindirectedenzymeevolutionviainsertiondeletionmutagenesis
AT devenishseanra accessingunexploredregionsofsequencespaceindirectedenzymeevolutionviainsertiondeletionmutagenesis
AT tokurikinobuhiko accessingunexploredregionsofsequencespaceindirectedenzymeevolutionviainsertiondeletionmutagenesis
AT hollfelderflorian accessingunexploredregionsofsequencespaceindirectedenzymeevolutionviainsertiondeletionmutagenesis