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Key reaction components affect the kinetics and performance robustness of cell-free protein synthesis reactions
Cell-free protein synthesis (CFPS) reactions have grown in popularity with particular interest in applications such as gene construct prototyping, biosensor technologies and the production of proteins with novel chemistry. Work has frequently focussed on optimising CFPS protocols for improving prote...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Research Network of Computational and Structural Biotechnology
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8718664/ https://www.ncbi.nlm.nih.gov/pubmed/35024094 http://dx.doi.org/10.1016/j.csbj.2021.12.013 |
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author | Banks, Alice M. Whitfield, Colette J. Brown, Steven R. Fulton, David A. Goodchild, Sarah A. Grant, Christopher Love, John Lendrem, Dennis W. Fieldsend, Jonathan E. Howard, Thomas P. |
author_facet | Banks, Alice M. Whitfield, Colette J. Brown, Steven R. Fulton, David A. Goodchild, Sarah A. Grant, Christopher Love, John Lendrem, Dennis W. Fieldsend, Jonathan E. Howard, Thomas P. |
author_sort | Banks, Alice M. |
collection | PubMed |
description | Cell-free protein synthesis (CFPS) reactions have grown in popularity with particular interest in applications such as gene construct prototyping, biosensor technologies and the production of proteins with novel chemistry. Work has frequently focussed on optimising CFPS protocols for improving protein yield, reducing cost, or developing streamlined production protocols. Here we describe a statistical Design of Experiments analysis of 20 components of a popular CFPS reaction buffer. We simultaneously identify factors and factor interactions that impact on protein yield, rate of reaction, lag time and reaction longevity. This systematic experimental approach enables the creation of a statistical model capturing multiple behaviours of CFPS reactions in response to components and their interactions. We show that a novel reaction buffer outperforms the reference reaction by 400% and importantly reduces failures in CFPS across batches of cell lysates, strains of E. coli, and in the synthesis of different proteins. Detailed and quantitative understanding of how reaction components affect kinetic responses and robustness is imperative for future deployment of cell-free technologies. |
format | Online Article Text |
id | pubmed-8718664 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Research Network of Computational and Structural Biotechnology |
record_format | MEDLINE/PubMed |
spelling | pubmed-87186642022-01-11 Key reaction components affect the kinetics and performance robustness of cell-free protein synthesis reactions Banks, Alice M. Whitfield, Colette J. Brown, Steven R. Fulton, David A. Goodchild, Sarah A. Grant, Christopher Love, John Lendrem, Dennis W. Fieldsend, Jonathan E. Howard, Thomas P. Comput Struct Biotechnol J Research Article Cell-free protein synthesis (CFPS) reactions have grown in popularity with particular interest in applications such as gene construct prototyping, biosensor technologies and the production of proteins with novel chemistry. Work has frequently focussed on optimising CFPS protocols for improving protein yield, reducing cost, or developing streamlined production protocols. Here we describe a statistical Design of Experiments analysis of 20 components of a popular CFPS reaction buffer. We simultaneously identify factors and factor interactions that impact on protein yield, rate of reaction, lag time and reaction longevity. This systematic experimental approach enables the creation of a statistical model capturing multiple behaviours of CFPS reactions in response to components and their interactions. We show that a novel reaction buffer outperforms the reference reaction by 400% and importantly reduces failures in CFPS across batches of cell lysates, strains of E. coli, and in the synthesis of different proteins. Detailed and quantitative understanding of how reaction components affect kinetic responses and robustness is imperative for future deployment of cell-free technologies. Research Network of Computational and Structural Biotechnology 2021-12-13 /pmc/articles/PMC8718664/ /pubmed/35024094 http://dx.doi.org/10.1016/j.csbj.2021.12.013 Text en © 2021 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Research Article Banks, Alice M. Whitfield, Colette J. Brown, Steven R. Fulton, David A. Goodchild, Sarah A. Grant, Christopher Love, John Lendrem, Dennis W. Fieldsend, Jonathan E. Howard, Thomas P. Key reaction components affect the kinetics and performance robustness of cell-free protein synthesis reactions |
title | Key reaction components affect the kinetics and performance robustness of cell-free protein synthesis reactions |
title_full | Key reaction components affect the kinetics and performance robustness of cell-free protein synthesis reactions |
title_fullStr | Key reaction components affect the kinetics and performance robustness of cell-free protein synthesis reactions |
title_full_unstemmed | Key reaction components affect the kinetics and performance robustness of cell-free protein synthesis reactions |
title_short | Key reaction components affect the kinetics and performance robustness of cell-free protein synthesis reactions |
title_sort | key reaction components affect the kinetics and performance robustness of cell-free protein synthesis reactions |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8718664/ https://www.ncbi.nlm.nih.gov/pubmed/35024094 http://dx.doi.org/10.1016/j.csbj.2021.12.013 |
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