Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
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
_version_ 1784912191101599744
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
work_keys_str_mv AT søgaardanebretschneider transmembranesignalingbyasyntheticreceptorinartificialcells
AT pedersenandreasbøtker transmembranesignalingbyasyntheticreceptorinartificialcells
AT løvschallkajaborup transmembranesignalingbyasyntheticreceptorinartificialcells
AT mongepere transmembranesignalingbyasyntheticreceptorinartificialcells
AT jakobsenjosefinehammer transmembranesignalingbyasyntheticreceptorinartificialcells
AT dzabbarovaleila transmembranesignalingbyasyntheticreceptorinartificialcells
AT nielsenlinefriis transmembranesignalingbyasyntheticreceptorinartificialcells
AT stevanovicsandra transmembranesignalingbyasyntheticreceptorinartificialcells
AT waltherraoul transmembranesignalingbyasyntheticreceptorinartificialcells
AT zelikinalexandern transmembranesignalingbyasyntheticreceptorinartificialcells