Enzyme controlled transient phospholipid vesicles for regulated cargo release
Metabolism in biological systems involves the continuous formation and breakdown of chemical and structural components, driven by chemical energy. In specific, metabolic processes on cellular membranes result in in situ formation and degradation of the constituent phospholipid molecules, by consumin...
| Autores: | , , , , , |
|---|---|
| Tipo de recurso: | artículo |
| Estado: | Versión publicada |
| Fecha de publicación: | 2025 |
| País: | España |
| Institución: | Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya) |
| Repositorio: | Recercat. Dipósit de la Recerca de Catalunya |
| OAI Identifier: | oai:recercat.cat:2445/222125 |
| Acceso en línea: | https://hdl.handle.net/2445/222125 |
| Access Level: | acceso abierto |
| Palabra clave: | Nanomedicina Membranes (Biologia) Fosfolípids Nanomedicine Membranes (Biology) Phospholipids |
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Enzyme controlled transient phospholipid vesicles for regulated cargo releaseVenugopal, AkhilGhosh, SubhadipCalò, AnnalisaTuveri, Gian MarcoBattaglia, GiuseppeKumar, MohitNanomedicinaMembranes (Biologia)FosfolípidsNanomedicineMembranes (Biology)PhospholipidsMetabolism in biological systems involves the continuous formation and breakdown of chemical and structural components, driven by chemical energy. In specific, metabolic processes on cellular membranes result in in situ formation and degradation of the constituent phospholipid molecules, by consuming fuel, to dynamically regulate the properties. Synthetic analogs of such chemically fueled phospholipid vesicles have been challenging. Here we report a bio-inspired approach for the in situ formation of phospholipids, from water soluble precursors, and their fuel driven self-assembly into vesicles. We show that the kinetic competition between anabolic and catabolic-like reactions leads to the formation and enzymatic degradation of the double-tailed, vesicle-forming phospholipid. Spectroscopic and microscopic analysis demonstrate the formation of transient vesicles whose lifetime can be easily tuned from minutes to hours. Importantly, our design results in the formation of uniform sized (65 nm) vesicles simply by mixing the precursors, thus avoiding the traditional complex methods. Finally, our sub-100 nm vesicles are of the right size for application in drug delivery. We have demonstrated that the release kinetics of the incorporated cargo molecules can be dynamically regulated for potential applications in adaptive nanomedicine.Wiley-VCH2025202520252025info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion7 p.application/pdfhttps://hdl.handle.net/2445/222125Articles publicats en revistes (Enginyeria Electrònica i Biomèdica)reponame:Recercat. Dipósit de la Recerca de Catalunyainstname:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)InglésReproducció del document publicat a: https://doi.org/10.1002/anie.202500824Angewandte Chemie-International Edition, 2025, vol. 64, num.20https://doi.org/10.1002/anie.202500824cc-by-nc (c) Venugopal et al., 2025http://creativecommons.org/licenses/by-nc/3.0/es/info:eu-repo/semantics/openAccessoai:recercat.cat:2445/2221252026-05-29T05:05:01Z |
| dc.title.none.fl_str_mv |
Enzyme controlled transient phospholipid vesicles for regulated cargo release |
| title |
Enzyme controlled transient phospholipid vesicles for regulated cargo release |
| spellingShingle |
Enzyme controlled transient phospholipid vesicles for regulated cargo release Venugopal, Akhil Nanomedicina Membranes (Biologia) Fosfolípids Nanomedicine Membranes (Biology) Phospholipids |
| title_short |
Enzyme controlled transient phospholipid vesicles for regulated cargo release |
| title_full |
Enzyme controlled transient phospholipid vesicles for regulated cargo release |
| title_fullStr |
Enzyme controlled transient phospholipid vesicles for regulated cargo release |
| title_full_unstemmed |
Enzyme controlled transient phospholipid vesicles for regulated cargo release |
| title_sort |
Enzyme controlled transient phospholipid vesicles for regulated cargo release |
| dc.creator.none.fl_str_mv |
Venugopal, Akhil Ghosh, Subhadip Calò, Annalisa Tuveri, Gian Marco Battaglia, Giuseppe Kumar, Mohit |
| author |
Venugopal, Akhil |
| author_facet |
Venugopal, Akhil Ghosh, Subhadip Calò, Annalisa Tuveri, Gian Marco Battaglia, Giuseppe Kumar, Mohit |
| author_role |
author |
| author2 |
Ghosh, Subhadip Calò, Annalisa Tuveri, Gian Marco Battaglia, Giuseppe Kumar, Mohit |
| author2_role |
author author author author author |
| dc.subject.none.fl_str_mv |
Nanomedicina Membranes (Biologia) Fosfolípids Nanomedicine Membranes (Biology) Phospholipids |
| topic |
Nanomedicina Membranes (Biologia) Fosfolípids Nanomedicine Membranes (Biology) Phospholipids |
| description |
Metabolism in biological systems involves the continuous formation and breakdown of chemical and structural components, driven by chemical energy. In specific, metabolic processes on cellular membranes result in in situ formation and degradation of the constituent phospholipid molecules, by consuming fuel, to dynamically regulate the properties. Synthetic analogs of such chemically fueled phospholipid vesicles have been challenging. Here we report a bio-inspired approach for the in situ formation of phospholipids, from water soluble precursors, and their fuel driven self-assembly into vesicles. We show that the kinetic competition between anabolic and catabolic-like reactions leads to the formation and enzymatic degradation of the double-tailed, vesicle-forming phospholipid. Spectroscopic and microscopic analysis demonstrate the formation of transient vesicles whose lifetime can be easily tuned from minutes to hours. Importantly, our design results in the formation of uniform sized (65 nm) vesicles simply by mixing the precursors, thus avoiding the traditional complex methods. Finally, our sub-100 nm vesicles are of the right size for application in drug delivery. We have demonstrated that the release kinetics of the incorporated cargo molecules can be dynamically regulated for potential applications in adaptive nanomedicine. |
| publishDate |
2025 |
| dc.date.none.fl_str_mv |
2025 2025 2025 2025 |
| dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion |
| format |
article |
| status_str |
publishedVersion |
| dc.identifier.none.fl_str_mv |
https://hdl.handle.net/2445/222125 |
| url |
https://hdl.handle.net/2445/222125 |
| dc.language.none.fl_str_mv |
Inglés |
| language_invalid_str_mv |
Inglés |
| dc.relation.none.fl_str_mv |
Reproducció del document publicat a: https://doi.org/10.1002/anie.202500824 Angewandte Chemie-International Edition, 2025, vol. 64, num.20 https://doi.org/10.1002/anie.202500824 |
| dc.rights.none.fl_str_mv |
cc-by-nc (c) Venugopal et al., 2025 http://creativecommons.org/licenses/by-nc/3.0/es/ info:eu-repo/semantics/openAccess |
| rights_invalid_str_mv |
cc-by-nc (c) Venugopal et al., 2025 http://creativecommons.org/licenses/by-nc/3.0/es/ |
| eu_rights_str_mv |
openAccess |
| dc.format.none.fl_str_mv |
7 p. application/pdf |
| dc.publisher.none.fl_str_mv |
Wiley-VCH |
| publisher.none.fl_str_mv |
Wiley-VCH |
| dc.source.none.fl_str_mv |
Articles publicats en revistes (Enginyeria Electrònica i Biomèdica) reponame:Recercat. Dipósit de la Recerca de Catalunya instname:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya) |
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Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya) |
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Recercat. Dipósit de la Recerca de Catalunya |
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Recercat. Dipósit de la Recerca de Catalunya |
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15,81155 |