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Triggered Polymersome Fusion
[Image: see text] The contents of biological cells are retained within compartments formed of phospholipid membranes. The movement of material within and between cells is often mediated by the fusion of phospholipid membranes, which allows mixing of contents or excretion of material into the surroun...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10021019/ https://www.ncbi.nlm.nih.gov/pubmed/36877655 http://dx.doi.org/10.1021/jacs.2c13049 |
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author | Fielden, Stephen D. P. Derry, Matthew J. Miller, Alisha J. Topham, Paul D. O’Reilly, Rachel K. |
author_facet | Fielden, Stephen D. P. Derry, Matthew J. Miller, Alisha J. Topham, Paul D. O’Reilly, Rachel K. |
author_sort | Fielden, Stephen D. P. |
collection | PubMed |
description | [Image: see text] The contents of biological cells are retained within compartments formed of phospholipid membranes. The movement of material within and between cells is often mediated by the fusion of phospholipid membranes, which allows mixing of contents or excretion of material into the surrounding environment. Biological membrane fusion is a highly regulated process that is catalyzed by proteins and often triggered by cellular signaling. In contrast, the controlled fusion of polymer-based membranes is largely unexplored, despite the potential application of this process in nanomedicine, smart materials, and reagent trafficking. Here, we demonstrate triggered polymersome fusion. Out-of-equilibrium polymersomes were formed by ring-opening metathesis polymerization-induced self-assembly and persist until a specific chemical signal (pH change) triggers their fusion. Characterization of polymersomes was performed by a variety of techniques, including dynamic light scattering, dry-state/cryogenic-transmission electron microscopy, and small-angle X-ray scattering (SAXS). The fusion process was followed by time-resolved SAXS analysis. Developing elementary methods of communication between polymersomes, such as fusion, will prove essential for emulating life-like behaviors in synthetic nanotechnology. |
format | Online Article Text |
id | pubmed-10021019 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-100210192023-03-18 Triggered Polymersome Fusion Fielden, Stephen D. P. Derry, Matthew J. Miller, Alisha J. Topham, Paul D. O’Reilly, Rachel K. J Am Chem Soc [Image: see text] The contents of biological cells are retained within compartments formed of phospholipid membranes. The movement of material within and between cells is often mediated by the fusion of phospholipid membranes, which allows mixing of contents or excretion of material into the surrounding environment. Biological membrane fusion is a highly regulated process that is catalyzed by proteins and often triggered by cellular signaling. In contrast, the controlled fusion of polymer-based membranes is largely unexplored, despite the potential application of this process in nanomedicine, smart materials, and reagent trafficking. Here, we demonstrate triggered polymersome fusion. Out-of-equilibrium polymersomes were formed by ring-opening metathesis polymerization-induced self-assembly and persist until a specific chemical signal (pH change) triggers their fusion. Characterization of polymersomes was performed by a variety of techniques, including dynamic light scattering, dry-state/cryogenic-transmission electron microscopy, and small-angle X-ray scattering (SAXS). The fusion process was followed by time-resolved SAXS analysis. Developing elementary methods of communication between polymersomes, such as fusion, will prove essential for emulating life-like behaviors in synthetic nanotechnology. American Chemical Society 2023-03-06 /pmc/articles/PMC10021019/ /pubmed/36877655 http://dx.doi.org/10.1021/jacs.2c13049 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Fielden, Stephen D. P. Derry, Matthew J. Miller, Alisha J. Topham, Paul D. O’Reilly, Rachel K. Triggered Polymersome Fusion |
title | Triggered Polymersome
Fusion |
title_full | Triggered Polymersome
Fusion |
title_fullStr | Triggered Polymersome
Fusion |
title_full_unstemmed | Triggered Polymersome
Fusion |
title_short | Triggered Polymersome
Fusion |
title_sort | triggered polymersome
fusion |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10021019/ https://www.ncbi.nlm.nih.gov/pubmed/36877655 http://dx.doi.org/10.1021/jacs.2c13049 |
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