Amyloid-polysaccharide interfacial coacervates as therapeutic materials
Autor(a) principal: | |
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Data de Publicação: | 2023 |
Outros Autores: | , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.1038/s41467-023-37629-z http://hdl.handle.net/11449/248639 |
Resumo: | Coacervation via liquid-liquid phase separation provides an excellent opportunity to address the challenges of designing nanostructured biomaterials with multiple functionalities. Protein-polysaccharide coacervates, in particular, offer an appealing strategy to target biomaterial scaffolds, but these systems suffer from the low mechanical and chemical stabilities of protein-based condensates. Here we overcome these limitations by transforming native proteins into amyloid fibrils and demonstrate that the coacervation of cationic protein amyloids and anionic linear polysaccharides results in the interfacial self-assembly of biomaterials with precise control of their structure and properties. The coacervates present a highly ordered asymmetric architecture with amyloid fibrils on one side and the polysaccharide on the other. We demonstrate the excellent performance of these coacervates for gastric ulcer protection by validating via an in vivo assay their therapeutic effect as engineered microparticles. These results point at amyloid-polysaccharides coacervates as an original and effective biomaterial for multiple uses in internal medicine. |
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Amyloid-polysaccharide interfacial coacervates as therapeutic materialsCoacervation via liquid-liquid phase separation provides an excellent opportunity to address the challenges of designing nanostructured biomaterials with multiple functionalities. Protein-polysaccharide coacervates, in particular, offer an appealing strategy to target biomaterial scaffolds, but these systems suffer from the low mechanical and chemical stabilities of protein-based condensates. Here we overcome these limitations by transforming native proteins into amyloid fibrils and demonstrate that the coacervation of cationic protein amyloids and anionic linear polysaccharides results in the interfacial self-assembly of biomaterials with precise control of their structure and properties. The coacervates present a highly ordered asymmetric architecture with amyloid fibrils on one side and the polysaccharide on the other. We demonstrate the excellent performance of these coacervates for gastric ulcer protection by validating via an in vivo assay their therapeutic effect as engineered microparticles. These results point at amyloid-polysaccharides coacervates as an original and effective biomaterial for multiple uses in internal medicine.ETH Zurich Department of Health Sciences and TechnologyETH Zurich Department of MaterialsPaul Scherrer Institute PSIDepartment of Drugs and Medicines School of Pharmaceutical Sciences São Paulo State University, Sao PauloDepartment of Biological Sciences School of Pharmaceutical Sciences São Paulo State University, Sao PauloDepartment of Drugs and Medicines School of Pharmaceutical Sciences São Paulo State University, Sao PauloDepartment of Biological Sciences School of Pharmaceutical Sciences São Paulo State University, Sao PauloETH ZurichPaul Scherrer Institute PSIUniversidade Estadual Paulista (UNESP)Peydayesh, MohammadKistler, SabrinaZhou, JiangtaoLutz-Bueno, VivianeVictorelli, Francesca DamianiMeneguin, Andréia Bagliotti [UNESP]Spósito, Larissa [UNESP]Bauab, Tais Maria [UNESP]Chorilli, Marlus [UNESP]Mezzenga, Raffaele2023-07-29T13:49:36Z2023-07-29T13:49:36Z2023-12-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://dx.doi.org/10.1038/s41467-023-37629-zNature Communications, v. 14, n. 1, 2023.2041-1723http://hdl.handle.net/11449/24863910.1038/s41467-023-37629-z2-s2.0-85151692538Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengNature Communicationsinfo:eu-repo/semantics/openAccess2024-06-24T13:46:00Zoai:repositorio.unesp.br:11449/248639Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T20:13:17.990374Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Amyloid-polysaccharide interfacial coacervates as therapeutic materials |
title |
Amyloid-polysaccharide interfacial coacervates as therapeutic materials |
spellingShingle |
Amyloid-polysaccharide interfacial coacervates as therapeutic materials Peydayesh, Mohammad |
title_short |
Amyloid-polysaccharide interfacial coacervates as therapeutic materials |
title_full |
Amyloid-polysaccharide interfacial coacervates as therapeutic materials |
title_fullStr |
Amyloid-polysaccharide interfacial coacervates as therapeutic materials |
title_full_unstemmed |
Amyloid-polysaccharide interfacial coacervates as therapeutic materials |
title_sort |
Amyloid-polysaccharide interfacial coacervates as therapeutic materials |
author |
Peydayesh, Mohammad |
author_facet |
Peydayesh, Mohammad Kistler, Sabrina Zhou, Jiangtao Lutz-Bueno, Viviane Victorelli, Francesca Damiani Meneguin, Andréia Bagliotti [UNESP] Spósito, Larissa [UNESP] Bauab, Tais Maria [UNESP] Chorilli, Marlus [UNESP] Mezzenga, Raffaele |
author_role |
author |
author2 |
Kistler, Sabrina Zhou, Jiangtao Lutz-Bueno, Viviane Victorelli, Francesca Damiani Meneguin, Andréia Bagliotti [UNESP] Spósito, Larissa [UNESP] Bauab, Tais Maria [UNESP] Chorilli, Marlus [UNESP] Mezzenga, Raffaele |
author2_role |
author author author author author author author author author |
dc.contributor.none.fl_str_mv |
ETH Zurich Paul Scherrer Institute PSI Universidade Estadual Paulista (UNESP) |
dc.contributor.author.fl_str_mv |
Peydayesh, Mohammad Kistler, Sabrina Zhou, Jiangtao Lutz-Bueno, Viviane Victorelli, Francesca Damiani Meneguin, Andréia Bagliotti [UNESP] Spósito, Larissa [UNESP] Bauab, Tais Maria [UNESP] Chorilli, Marlus [UNESP] Mezzenga, Raffaele |
description |
Coacervation via liquid-liquid phase separation provides an excellent opportunity to address the challenges of designing nanostructured biomaterials with multiple functionalities. Protein-polysaccharide coacervates, in particular, offer an appealing strategy to target biomaterial scaffolds, but these systems suffer from the low mechanical and chemical stabilities of protein-based condensates. Here we overcome these limitations by transforming native proteins into amyloid fibrils and demonstrate that the coacervation of cationic protein amyloids and anionic linear polysaccharides results in the interfacial self-assembly of biomaterials with precise control of their structure and properties. The coacervates present a highly ordered asymmetric architecture with amyloid fibrils on one side and the polysaccharide on the other. We demonstrate the excellent performance of these coacervates for gastric ulcer protection by validating via an in vivo assay their therapeutic effect as engineered microparticles. These results point at amyloid-polysaccharides coacervates as an original and effective biomaterial for multiple uses in internal medicine. |
publishDate |
2023 |
dc.date.none.fl_str_mv |
2023-07-29T13:49:36Z 2023-07-29T13:49:36Z 2023-12-01 |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1038/s41467-023-37629-z Nature Communications, v. 14, n. 1, 2023. 2041-1723 http://hdl.handle.net/11449/248639 10.1038/s41467-023-37629-z 2-s2.0-85151692538 |
url |
http://dx.doi.org/10.1038/s41467-023-37629-z http://hdl.handle.net/11449/248639 |
identifier_str_mv |
Nature Communications, v. 14, n. 1, 2023. 2041-1723 10.1038/s41467-023-37629-z 2-s2.0-85151692538 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Nature Communications |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.source.none.fl_str_mv |
Scopus reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
institution |
UNESP |
reponame_str |
Repositório Institucional da UNESP |
collection |
Repositório Institucional da UNESP |
repository.name.fl_str_mv |
Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
|
_version_ |
1808129174130393088 |