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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
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.
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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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