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High Macromolecular Crowding in Liposomes from Microfluidics
The intracellular environment is crowded with macromolecules that influence biochemical equilibria and biomacromolecule diffusion. The incorporation of such crowding in synthetic cells would be needed to mimic the biochemistry of living cells. However, only a few methods provide crowded artificial c...
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/PMC9507340/ https://www.ncbi.nlm.nih.gov/pubmed/35904258 http://dx.doi.org/10.1002/advs.202201169 |
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author | Guerzoni, Luis P. B. de Goes, André V. C. Kalacheva, Milara Haduła, Jakub Mork, Matthias De Laporte, Laura Boersma, Arnold J. |
author_facet | Guerzoni, Luis P. B. de Goes, André V. C. Kalacheva, Milara Haduła, Jakub Mork, Matthias De Laporte, Laura Boersma, Arnold J. |
author_sort | Guerzoni, Luis P. B. |
collection | PubMed |
description | The intracellular environment is crowded with macromolecules that influence biochemical equilibria and biomacromolecule diffusion. The incorporation of such crowding in synthetic cells would be needed to mimic the biochemistry of living cells. However, only a few methods provide crowded artificial cells, moreover providing cells with either heterogeneous size and composition or containing a significant oil fraction. Therefore, a method that generates monodisperse liposomes with minimal oil content and tunable macromolecular crowding using polydimethylsiloxane (PDMS)‐based microfluidics is presented. Lipid stabilized water‐in‐oil‐in‐water emulsions that are stable for at least several months and with a high macromolecular crowder concentration that can be controlled with the external osmolality are formed. A crucial feature is that the oil phase can be removed using high flow conditions at any point after production, providing the highly crowded liposomes. Genetically encoded macromolecular crowding sensors show that the high level of macromolecular crowding in the emulsions is fully retained throughout the generation of minimal‐oil lipid bilayers. This modular and robust platform will serve the study of biochemistry under physiologically relevant crowding conditions. |
format | Online Article Text |
id | pubmed-9507340 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95073402022-09-30 High Macromolecular Crowding in Liposomes from Microfluidics Guerzoni, Luis P. B. de Goes, André V. C. Kalacheva, Milara Haduła, Jakub Mork, Matthias De Laporte, Laura Boersma, Arnold J. Adv Sci (Weinh) Research Articles The intracellular environment is crowded with macromolecules that influence biochemical equilibria and biomacromolecule diffusion. The incorporation of such crowding in synthetic cells would be needed to mimic the biochemistry of living cells. However, only a few methods provide crowded artificial cells, moreover providing cells with either heterogeneous size and composition or containing a significant oil fraction. Therefore, a method that generates monodisperse liposomes with minimal oil content and tunable macromolecular crowding using polydimethylsiloxane (PDMS)‐based microfluidics is presented. Lipid stabilized water‐in‐oil‐in‐water emulsions that are stable for at least several months and with a high macromolecular crowder concentration that can be controlled with the external osmolality are formed. A crucial feature is that the oil phase can be removed using high flow conditions at any point after production, providing the highly crowded liposomes. Genetically encoded macromolecular crowding sensors show that the high level of macromolecular crowding in the emulsions is fully retained throughout the generation of minimal‐oil lipid bilayers. This modular and robust platform will serve the study of biochemistry under physiologically relevant crowding conditions. John Wiley and Sons Inc. 2022-07-29 /pmc/articles/PMC9507340/ /pubmed/35904258 http://dx.doi.org/10.1002/advs.202201169 Text en © 2022 The Authors. Advanced Science 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 | Research Articles Guerzoni, Luis P. B. de Goes, André V. C. Kalacheva, Milara Haduła, Jakub Mork, Matthias De Laporte, Laura Boersma, Arnold J. High Macromolecular Crowding in Liposomes from Microfluidics |
title | High Macromolecular Crowding in Liposomes from Microfluidics |
title_full | High Macromolecular Crowding in Liposomes from Microfluidics |
title_fullStr | High Macromolecular Crowding in Liposomes from Microfluidics |
title_full_unstemmed | High Macromolecular Crowding in Liposomes from Microfluidics |
title_short | High Macromolecular Crowding in Liposomes from Microfluidics |
title_sort | high macromolecular crowding in liposomes from microfluidics |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9507340/ https://www.ncbi.nlm.nih.gov/pubmed/35904258 http://dx.doi.org/10.1002/advs.202201169 |
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