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Highly efficient libraries design for saturation mutagenesis
Saturation mutagenesis is a semi-rational approach for protein engineering where sites are saturated either entirely or partially to include amino acids of interest. We previously reported on a codon compression algorithm, where a set of minimal degenerate codons are selected according to user-defin...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9205323/ https://www.ncbi.nlm.nih.gov/pubmed/35734540 http://dx.doi.org/10.1093/synbio/ysac006 |
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author | Pines, Gur Pines, Assaf Eckert, Carrie A |
author_facet | Pines, Gur Pines, Assaf Eckert, Carrie A |
author_sort | Pines, Gur |
collection | PubMed |
description | Saturation mutagenesis is a semi-rational approach for protein engineering where sites are saturated either entirely or partially to include amino acids of interest. We previously reported on a codon compression algorithm, where a set of minimal degenerate codons are selected according to user-defined parameters such as the target organism, type of saturation and usage levels. Here, we communicate an addition to our web tool that considers the distance between the wild-type codon and the library, depending on its purpose. These forms of restricted collections further reduce library size, lowering downstream screening efforts or, in turn, allowing more comprehensive saturation of multiple sites. The library design tool can be accessed via http://www.dynamcc.com/dynamcc_d/. Graphical Abstract [Image: see text] |
format | Online Article Text |
id | pubmed-9205323 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-92053232022-06-21 Highly efficient libraries design for saturation mutagenesis Pines, Gur Pines, Assaf Eckert, Carrie A Synth Biol (Oxf) Software Saturation mutagenesis is a semi-rational approach for protein engineering where sites are saturated either entirely or partially to include amino acids of interest. We previously reported on a codon compression algorithm, where a set of minimal degenerate codons are selected according to user-defined parameters such as the target organism, type of saturation and usage levels. Here, we communicate an addition to our web tool that considers the distance between the wild-type codon and the library, depending on its purpose. These forms of restricted collections further reduce library size, lowering downstream screening efforts or, in turn, allowing more comprehensive saturation of multiple sites. The library design tool can be accessed via http://www.dynamcc.com/dynamcc_d/. Graphical Abstract [Image: see text] Oxford University Press 2022-04-28 /pmc/articles/PMC9205323/ /pubmed/35734540 http://dx.doi.org/10.1093/synbio/ysac006 Text en © The Author(s) 2022. Published by Oxford University Press. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Software Pines, Gur Pines, Assaf Eckert, Carrie A Highly efficient libraries design for saturation mutagenesis |
title | Highly efficient libraries design for saturation mutagenesis |
title_full | Highly efficient libraries design for saturation mutagenesis |
title_fullStr | Highly efficient libraries design for saturation mutagenesis |
title_full_unstemmed | Highly efficient libraries design for saturation mutagenesis |
title_short | Highly efficient libraries design for saturation mutagenesis |
title_sort | highly efficient libraries design for saturation mutagenesis |
topic | Software |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9205323/ https://www.ncbi.nlm.nih.gov/pubmed/35734540 http://dx.doi.org/10.1093/synbio/ysac006 |
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