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Towards synthetic cells using peptide-based reaction compartments
Membrane compartmentalization and growth are central aspects of living cells, and are thus encoded in every cell’s genome. For the creation of artificial cellular systems, genetic information and production of membrane building blocks will need to be coupled in a similar manner. However, natural bio...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6154970/ https://www.ncbi.nlm.nih.gov/pubmed/30242152 http://dx.doi.org/10.1038/s41467-018-06379-8 |
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author | Vogele, Kilian Frank, Thomas Gasser, Lukas Goetzfried, Marisa A. Hackl, Mathias W. Sieber, Stephan A. Simmel, Friedrich C. Pirzer, Tobias |
author_facet | Vogele, Kilian Frank, Thomas Gasser, Lukas Goetzfried, Marisa A. Hackl, Mathias W. Sieber, Stephan A. Simmel, Friedrich C. Pirzer, Tobias |
author_sort | Vogele, Kilian |
collection | PubMed |
description | Membrane compartmentalization and growth are central aspects of living cells, and are thus encoded in every cell’s genome. For the creation of artificial cellular systems, genetic information and production of membrane building blocks will need to be coupled in a similar manner. However, natural biochemical reaction networks and membrane building blocks are notoriously difficult to implement in vitro. Here, we utilized amphiphilic elastin-like peptides (ELP) to create self-assembled vesicular structures of about 200 nm diameter. In order to genetically encode the growth of these vesicles, we encapsulate a cell-free transcription-translation system together with the DNA template inside the peptide vesicles. We show in vesiculo production of a functioning fluorescent RNA aptamer and a fluorescent protein. Furthermore, we implement in situ expression of the membrane peptide itself and finally demonstrate autonomous vesicle growth due to the incorporation of this ELP into the membrane. |
format | Online Article Text |
id | pubmed-6154970 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-61549702018-09-28 Towards synthetic cells using peptide-based reaction compartments Vogele, Kilian Frank, Thomas Gasser, Lukas Goetzfried, Marisa A. Hackl, Mathias W. Sieber, Stephan A. Simmel, Friedrich C. Pirzer, Tobias Nat Commun Article Membrane compartmentalization and growth are central aspects of living cells, and are thus encoded in every cell’s genome. For the creation of artificial cellular systems, genetic information and production of membrane building blocks will need to be coupled in a similar manner. However, natural biochemical reaction networks and membrane building blocks are notoriously difficult to implement in vitro. Here, we utilized amphiphilic elastin-like peptides (ELP) to create self-assembled vesicular structures of about 200 nm diameter. In order to genetically encode the growth of these vesicles, we encapsulate a cell-free transcription-translation system together with the DNA template inside the peptide vesicles. We show in vesiculo production of a functioning fluorescent RNA aptamer and a fluorescent protein. Furthermore, we implement in situ expression of the membrane peptide itself and finally demonstrate autonomous vesicle growth due to the incorporation of this ELP into the membrane. Nature Publishing Group UK 2018-09-21 /pmc/articles/PMC6154970/ /pubmed/30242152 http://dx.doi.org/10.1038/s41467-018-06379-8 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 Vogele, Kilian Frank, Thomas Gasser, Lukas Goetzfried, Marisa A. Hackl, Mathias W. Sieber, Stephan A. Simmel, Friedrich C. Pirzer, Tobias Towards synthetic cells using peptide-based reaction compartments |
title | Towards synthetic cells using peptide-based reaction compartments |
title_full | Towards synthetic cells using peptide-based reaction compartments |
title_fullStr | Towards synthetic cells using peptide-based reaction compartments |
title_full_unstemmed | Towards synthetic cells using peptide-based reaction compartments |
title_short | Towards synthetic cells using peptide-based reaction compartments |
title_sort | towards synthetic cells using peptide-based reaction compartments |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6154970/ https://www.ncbi.nlm.nih.gov/pubmed/30242152 http://dx.doi.org/10.1038/s41467-018-06379-8 |
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