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Self-assembly–based posttranslational protein oscillators

Recent advances in synthetic posttranslational protein circuits are substantially impacting the landscape of cellular engineering and offer several advantages compared to traditional gene circuits. However, engineering dynamic phenomena such as oscillations in protein-level circuits remains an outst...

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Detalles Bibliográficos
Autores principales: Kimchi, Ofer, Goodrich, Carl P., Courbet, Alexis, Curatolo, Agnese I., Woodall, Nicholas B., Baker, David, Brenner, Michael P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7744077/
https://www.ncbi.nlm.nih.gov/pubmed/33328225
http://dx.doi.org/10.1126/sciadv.abc1939
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author Kimchi, Ofer
Goodrich, Carl P.
Courbet, Alexis
Curatolo, Agnese I.
Woodall, Nicholas B.
Baker, David
Brenner, Michael P.
author_facet Kimchi, Ofer
Goodrich, Carl P.
Courbet, Alexis
Curatolo, Agnese I.
Woodall, Nicholas B.
Baker, David
Brenner, Michael P.
author_sort Kimchi, Ofer
collection PubMed
description Recent advances in synthetic posttranslational protein circuits are substantially impacting the landscape of cellular engineering and offer several advantages compared to traditional gene circuits. However, engineering dynamic phenomena such as oscillations in protein-level circuits remains an outstanding challenge. Few examples of biological posttranslational oscillators are known, necessitating theoretical progress to determine realizable oscillators. We construct mathematical models for two posttranslational oscillators, using few components that interact only through reversible binding and phosphorylation/dephosphorylation reactions. Our designed oscillators rely on the self-assembly of two protein species into multimeric functional enzymes that respectively inhibit and enhance this self-assembly. We limit our analysis to within experimental constraints, finding (i) significant portions of the restricted parameter space yielding oscillations and (ii) that oscillation periods can be tuned by several orders of magnitude using recent advances in computational protein design. Our work paves the way for the rational design and realization of protein-based dynamic systems.
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spelling pubmed-77440772021-01-04 Self-assembly–based posttranslational protein oscillators Kimchi, Ofer Goodrich, Carl P. Courbet, Alexis Curatolo, Agnese I. Woodall, Nicholas B. Baker, David Brenner, Michael P. Sci Adv Research Articles Recent advances in synthetic posttranslational protein circuits are substantially impacting the landscape of cellular engineering and offer several advantages compared to traditional gene circuits. However, engineering dynamic phenomena such as oscillations in protein-level circuits remains an outstanding challenge. Few examples of biological posttranslational oscillators are known, necessitating theoretical progress to determine realizable oscillators. We construct mathematical models for two posttranslational oscillators, using few components that interact only through reversible binding and phosphorylation/dephosphorylation reactions. Our designed oscillators rely on the self-assembly of two protein species into multimeric functional enzymes that respectively inhibit and enhance this self-assembly. We limit our analysis to within experimental constraints, finding (i) significant portions of the restricted parameter space yielding oscillations and (ii) that oscillation periods can be tuned by several orders of magnitude using recent advances in computational protein design. Our work paves the way for the rational design and realization of protein-based dynamic systems. American Association for the Advancement of Science 2020-12-16 /pmc/articles/PMC7744077/ /pubmed/33328225 http://dx.doi.org/10.1126/sciadv.abc1939 Text en Copyright © 2020 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution License 4.0 (CC BY). https://creativecommons.org/licenses/by/4.0/ https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution license (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Kimchi, Ofer
Goodrich, Carl P.
Courbet, Alexis
Curatolo, Agnese I.
Woodall, Nicholas B.
Baker, David
Brenner, Michael P.
Self-assembly–based posttranslational protein oscillators
title Self-assembly–based posttranslational protein oscillators
title_full Self-assembly–based posttranslational protein oscillators
title_fullStr Self-assembly–based posttranslational protein oscillators
title_full_unstemmed Self-assembly–based posttranslational protein oscillators
title_short Self-assembly–based posttranslational protein oscillators
title_sort self-assembly–based posttranslational protein oscillators
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7744077/
https://www.ncbi.nlm.nih.gov/pubmed/33328225
http://dx.doi.org/10.1126/sciadv.abc1939
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