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DNA‐Mediated Protein Shuttling between Coacervate‐Based Artificial Cells
The regulation of protein uptake and secretion is crucial for (inter)cellular signaling. Mimicking these molecular events is essential when engineering synthetic cellular systems. A first step towards achieving this goal is obtaining control over the uptake and release of proteins from synthetic cel...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9303767/ https://www.ncbi.nlm.nih.gov/pubmed/35133040 http://dx.doi.org/10.1002/anie.202115041 |
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author | Mashima, Tsuyoshi van Stevendaal, Marleen H. M. E. Cornelissens, Femke R. A. Mason, Alexander F. Rosier, Bas J. H. M. Altenburg, Wiggert J. Oohora, Koji Hirayama, Shota Hayashi, Takashi van Hest, Jan C. M. Brunsveld, Luc |
author_facet | Mashima, Tsuyoshi van Stevendaal, Marleen H. M. E. Cornelissens, Femke R. A. Mason, Alexander F. Rosier, Bas J. H. M. Altenburg, Wiggert J. Oohora, Koji Hirayama, Shota Hayashi, Takashi van Hest, Jan C. M. Brunsveld, Luc |
author_sort | Mashima, Tsuyoshi |
collection | PubMed |
description | The regulation of protein uptake and secretion is crucial for (inter)cellular signaling. Mimicking these molecular events is essential when engineering synthetic cellular systems. A first step towards achieving this goal is obtaining control over the uptake and release of proteins from synthetic cells in response to an external trigger. Herein, we have developed an artificial cell that sequesters and releases proteinaceous cargo upon addition of a coded chemical signal: single‐stranded DNA oligos (ssDNA) were employed to independently control the localization of a set of three different ssDNA‐modified proteins. The molecular coded signal allows for multiple iterations of triggered uptake and release, regulation of the amount and rate of protein release and the sequential release of the three different proteins. This signaling concept was furthermore used to directionally transfer a protein between two artificial cell populations, providing novel directions for engineering lifelike communication pathways inside higher order (proto)cellular structures. |
format | Online Article Text |
id | pubmed-9303767 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-93037672022-07-28 DNA‐Mediated Protein Shuttling between Coacervate‐Based Artificial Cells Mashima, Tsuyoshi van Stevendaal, Marleen H. M. E. Cornelissens, Femke R. A. Mason, Alexander F. Rosier, Bas J. H. M. Altenburg, Wiggert J. Oohora, Koji Hirayama, Shota Hayashi, Takashi van Hest, Jan C. M. Brunsveld, Luc Angew Chem Int Ed Engl Communications The regulation of protein uptake and secretion is crucial for (inter)cellular signaling. Mimicking these molecular events is essential when engineering synthetic cellular systems. A first step towards achieving this goal is obtaining control over the uptake and release of proteins from synthetic cells in response to an external trigger. Herein, we have developed an artificial cell that sequesters and releases proteinaceous cargo upon addition of a coded chemical signal: single‐stranded DNA oligos (ssDNA) were employed to independently control the localization of a set of three different ssDNA‐modified proteins. The molecular coded signal allows for multiple iterations of triggered uptake and release, regulation of the amount and rate of protein release and the sequential release of the three different proteins. This signaling concept was furthermore used to directionally transfer a protein between two artificial cell populations, providing novel directions for engineering lifelike communication pathways inside higher order (proto)cellular structures. John Wiley and Sons Inc. 2022-02-26 2022-04-19 /pmc/articles/PMC9303767/ /pubmed/35133040 http://dx.doi.org/10.1002/anie.202115041 Text en © 2022 The Authors. Angewandte Chemie International Edition published by Wiley-VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Communications Mashima, Tsuyoshi van Stevendaal, Marleen H. M. E. Cornelissens, Femke R. A. Mason, Alexander F. Rosier, Bas J. H. M. Altenburg, Wiggert J. Oohora, Koji Hirayama, Shota Hayashi, Takashi van Hest, Jan C. M. Brunsveld, Luc DNA‐Mediated Protein Shuttling between Coacervate‐Based Artificial Cells |
title | DNA‐Mediated Protein Shuttling between Coacervate‐Based Artificial Cells |
title_full | DNA‐Mediated Protein Shuttling between Coacervate‐Based Artificial Cells |
title_fullStr | DNA‐Mediated Protein Shuttling between Coacervate‐Based Artificial Cells |
title_full_unstemmed | DNA‐Mediated Protein Shuttling between Coacervate‐Based Artificial Cells |
title_short | DNA‐Mediated Protein Shuttling between Coacervate‐Based Artificial Cells |
title_sort | dna‐mediated protein shuttling between coacervate‐based artificial cells |
topic | Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9303767/ https://www.ncbi.nlm.nih.gov/pubmed/35133040 http://dx.doi.org/10.1002/anie.202115041 |
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