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Strategies for protein synthetic biology
Proteins are the most versatile among the various biological building blocks and a mature field of protein engineering has lead to many industrial and biomedical applications. But the strength of proteins—their versatility, dynamics and interactions—also complicates and hinders systems engineering....
Autores principales: | , |
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Formato: | Texto |
Lenguaje: | English |
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Oxford University Press
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2860127/ https://www.ncbi.nlm.nih.gov/pubmed/20385577 http://dx.doi.org/10.1093/nar/gkq139 |
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author | Grünberg, Raik Serrano, Luis |
author_facet | Grünberg, Raik Serrano, Luis |
author_sort | Grünberg, Raik |
collection | PubMed |
description | Proteins are the most versatile among the various biological building blocks and a mature field of protein engineering has lead to many industrial and biomedical applications. But the strength of proteins—their versatility, dynamics and interactions—also complicates and hinders systems engineering. Therefore, the design of more sophisticated, multi-component protein systems appears to lag behind, in particular, when compared to the engineering of gene regulatory networks. Yet, synthetic biologists have started to tinker with the information flow through natural signaling networks or integrated protein switches. A successful strategy common to most of these experiments is their focus on modular interactions between protein domains or domains and peptide motifs. Such modular interaction swapping has rewired signaling in yeast, put mammalian cell morphology under the control of light, or increased the flux through a synthetic metabolic pathway. Based on this experience, we outline an engineering framework for the connection of reusable protein interaction devices into self-sufficient circuits. Such a framework should help to ‘refacture’ protein complexity into well-defined exchangeable devices for predictive engineering. We review the foundations and initial success stories of protein synthetic biology and discuss the challenges and promises on the way from protein- to protein systems design. |
format | Text |
id | pubmed-2860127 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-28601272010-04-27 Strategies for protein synthetic biology Grünberg, Raik Serrano, Luis Nucleic Acids Res Synthetic Biology and Chemistry Proteins are the most versatile among the various biological building blocks and a mature field of protein engineering has lead to many industrial and biomedical applications. But the strength of proteins—their versatility, dynamics and interactions—also complicates and hinders systems engineering. Therefore, the design of more sophisticated, multi-component protein systems appears to lag behind, in particular, when compared to the engineering of gene regulatory networks. Yet, synthetic biologists have started to tinker with the information flow through natural signaling networks or integrated protein switches. A successful strategy common to most of these experiments is their focus on modular interactions between protein domains or domains and peptide motifs. Such modular interaction swapping has rewired signaling in yeast, put mammalian cell morphology under the control of light, or increased the flux through a synthetic metabolic pathway. Based on this experience, we outline an engineering framework for the connection of reusable protein interaction devices into self-sufficient circuits. Such a framework should help to ‘refacture’ protein complexity into well-defined exchangeable devices for predictive engineering. We review the foundations and initial success stories of protein synthetic biology and discuss the challenges and promises on the way from protein- to protein systems design. Oxford University Press 2010-05 2010-04-12 /pmc/articles/PMC2860127/ /pubmed/20385577 http://dx.doi.org/10.1093/nar/gkq139 Text en © The Author(s) 2010. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/2.5 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.5), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Synthetic Biology and Chemistry Grünberg, Raik Serrano, Luis Strategies for protein synthetic biology |
title | Strategies for protein synthetic biology |
title_full | Strategies for protein synthetic biology |
title_fullStr | Strategies for protein synthetic biology |
title_full_unstemmed | Strategies for protein synthetic biology |
title_short | Strategies for protein synthetic biology |
title_sort | strategies for protein synthetic biology |
topic | Synthetic Biology and Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2860127/ https://www.ncbi.nlm.nih.gov/pubmed/20385577 http://dx.doi.org/10.1093/nar/gkq139 |
work_keys_str_mv | AT grunbergraik strategiesforproteinsyntheticbiology AT serranoluis strategiesforproteinsyntheticbiology |