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Anomalous Scaling of Gene Expression in Confined Cell-Free Reactions

Cellular surface breaks the symmetry of molecular diffusion across membrane. Here, we study how steric interactions between the surface and the bulk of cell-sized emulsion droplets alters gene expression emulated by a cell-free transcription/translation (TXTL) system. The concentration of synthesize...

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Detalles Bibliográficos
Autores principales: Sakamoto, Ryota, Noireaux, Vincent, Maeda, Yusuke T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5943292/
https://www.ncbi.nlm.nih.gov/pubmed/29743508
http://dx.doi.org/10.1038/s41598-018-25532-3
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author Sakamoto, Ryota
Noireaux, Vincent
Maeda, Yusuke T.
author_facet Sakamoto, Ryota
Noireaux, Vincent
Maeda, Yusuke T.
author_sort Sakamoto, Ryota
collection PubMed
description Cellular surface breaks the symmetry of molecular diffusion across membrane. Here, we study how steric interactions between the surface and the bulk of cell-sized emulsion droplets alters gene expression emulated by a cell-free transcription/translation (TXTL) system. The concentration of synthesized reporter proteins in droplets of radius R shows an anomalous geometric scaling of R(4) different from the expected size-dependence of R(3). Given that TXTL becomes less efficient at thin surface layer, a mathematical model explains the anomalous size-dependence found in experiment. The surface of cell-sized compartment can thus play a regulatory role for cell-free gene expression.
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spelling pubmed-59432922018-05-14 Anomalous Scaling of Gene Expression in Confined Cell-Free Reactions Sakamoto, Ryota Noireaux, Vincent Maeda, Yusuke T. Sci Rep Article Cellular surface breaks the symmetry of molecular diffusion across membrane. Here, we study how steric interactions between the surface and the bulk of cell-sized emulsion droplets alters gene expression emulated by a cell-free transcription/translation (TXTL) system. The concentration of synthesized reporter proteins in droplets of radius R shows an anomalous geometric scaling of R(4) different from the expected size-dependence of R(3). Given that TXTL becomes less efficient at thin surface layer, a mathematical model explains the anomalous size-dependence found in experiment. The surface of cell-sized compartment can thus play a regulatory role for cell-free gene expression. Nature Publishing Group UK 2018-05-09 /pmc/articles/PMC5943292/ /pubmed/29743508 http://dx.doi.org/10.1038/s41598-018-25532-3 Text en © The Author(s) 2018 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
Sakamoto, Ryota
Noireaux, Vincent
Maeda, Yusuke T.
Anomalous Scaling of Gene Expression in Confined Cell-Free Reactions
title Anomalous Scaling of Gene Expression in Confined Cell-Free Reactions
title_full Anomalous Scaling of Gene Expression in Confined Cell-Free Reactions
title_fullStr Anomalous Scaling of Gene Expression in Confined Cell-Free Reactions
title_full_unstemmed Anomalous Scaling of Gene Expression in Confined Cell-Free Reactions
title_short Anomalous Scaling of Gene Expression in Confined Cell-Free Reactions
title_sort anomalous scaling of gene expression in confined cell-free reactions
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5943292/
https://www.ncbi.nlm.nih.gov/pubmed/29743508
http://dx.doi.org/10.1038/s41598-018-25532-3
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