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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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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 |
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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 |
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