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Transmembrane signaling by a synthetic receptor in artificial cells
Signal transduction across biological membranes is among the most important evolutionary achievements. Herein, for the design of artificial cells, we engineer fully synthetic receptors with the capacity of transmembrane signaling, using tools of chemistry. Our receptors exhibit similarity with their...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10039019/ https://www.ncbi.nlm.nih.gov/pubmed/36964156 http://dx.doi.org/10.1038/s41467-023-37393-0 |
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author | Søgaard, Ane Bretschneider Pedersen, Andreas Bøtker Løvschall, Kaja Borup Monge, Pere Jakobsen, Josefine Hammer Džabbarova, Leila Nielsen, Line Friis Stevanovic, Sandra Walther, Raoul Zelikin, Alexander N. |
author_facet | Søgaard, Ane Bretschneider Pedersen, Andreas Bøtker Løvschall, Kaja Borup Monge, Pere Jakobsen, Josefine Hammer Džabbarova, Leila Nielsen, Line Friis Stevanovic, Sandra Walther, Raoul Zelikin, Alexander N. |
author_sort | Søgaard, Ane Bretschneider |
collection | PubMed |
description | Signal transduction across biological membranes is among the most important evolutionary achievements. Herein, for the design of artificial cells, we engineer fully synthetic receptors with the capacity of transmembrane signaling, using tools of chemistry. Our receptors exhibit similarity with their natural counterparts in having an exofacial ligand for signal capture, being membrane anchored, and featuring a releasable messenger molecule that performs enzyme activation as a downstream signaling event. The main difference from natural receptors is the mechanism of signal transduction, which is achieved using a self-immolative linker. The receptor scaffold is modular and can readily be re-designed to respond to diverse activation signals including biological or chemical stimuli. We demonstrate an artificial signaling cascade that achieves transmembrane enzyme activation, a hallmark of natural signaling receptors. Results of this work are relevant for engineering responsive artificial cells and interfacing them and/or biological counterparts in co-cultures. |
format | Online Article Text |
id | pubmed-10039019 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-100390192023-03-26 Transmembrane signaling by a synthetic receptor in artificial cells Søgaard, Ane Bretschneider Pedersen, Andreas Bøtker Løvschall, Kaja Borup Monge, Pere Jakobsen, Josefine Hammer Džabbarova, Leila Nielsen, Line Friis Stevanovic, Sandra Walther, Raoul Zelikin, Alexander N. Nat Commun Article Signal transduction across biological membranes is among the most important evolutionary achievements. Herein, for the design of artificial cells, we engineer fully synthetic receptors with the capacity of transmembrane signaling, using tools of chemistry. Our receptors exhibit similarity with their natural counterparts in having an exofacial ligand for signal capture, being membrane anchored, and featuring a releasable messenger molecule that performs enzyme activation as a downstream signaling event. The main difference from natural receptors is the mechanism of signal transduction, which is achieved using a self-immolative linker. The receptor scaffold is modular and can readily be re-designed to respond to diverse activation signals including biological or chemical stimuli. We demonstrate an artificial signaling cascade that achieves transmembrane enzyme activation, a hallmark of natural signaling receptors. Results of this work are relevant for engineering responsive artificial cells and interfacing them and/or biological counterparts in co-cultures. Nature Publishing Group UK 2023-03-24 /pmc/articles/PMC10039019/ /pubmed/36964156 http://dx.doi.org/10.1038/s41467-023-37393-0 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Søgaard, Ane Bretschneider Pedersen, Andreas Bøtker Løvschall, Kaja Borup Monge, Pere Jakobsen, Josefine Hammer Džabbarova, Leila Nielsen, Line Friis Stevanovic, Sandra Walther, Raoul Zelikin, Alexander N. Transmembrane signaling by a synthetic receptor in artificial cells |
title | Transmembrane signaling by a synthetic receptor in artificial cells |
title_full | Transmembrane signaling by a synthetic receptor in artificial cells |
title_fullStr | Transmembrane signaling by a synthetic receptor in artificial cells |
title_full_unstemmed | Transmembrane signaling by a synthetic receptor in artificial cells |
title_short | Transmembrane signaling by a synthetic receptor in artificial cells |
title_sort | transmembrane signaling by a synthetic receptor in artificial cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10039019/ https://www.ncbi.nlm.nih.gov/pubmed/36964156 http://dx.doi.org/10.1038/s41467-023-37393-0 |
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