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Article: Dual Self-Assembled Nanostructures from Intrinsically Disordered Protein Polymers with LCST Behavior and Antimicrobial Peptides

TitleDual Self-Assembled Nanostructures from Intrinsically Disordered Protein Polymers with LCST Behavior and Antimicrobial Peptides
Authors
Issue Date2020
Citation
Biomacromolecules, 2020, v. 21, n. 10, p. 4043-4052 How to Cite?
AbstractAntimicrobial peptides (AMPs) have attracted great interest as they constitute one of the most promising alternatives against drug-resistant infections. Their amphipathic nature not only provides them antimicrobial and immunomodulatory properties but also the ability to self-assemble into supramolecular nanostructures. Here, we propose their use as self-assembling domains to drive hierarchical organization of intrinsically disordered protein polymers (IDPPs). Using a modular approach, hybrid protein-engineered polymers were recombinantly produced, thus combining designer AMPs and a thermoresponsive IDPP, an elastin-like recombinamer (ELR). We exploited the ability of these AMPs and ELRs to self-assemble to develop supramolecular nanomaterials by way of a dual-assembly process. First, the AMPs trigger the formation of nanofibers; then, the thermoresponsiveness of the ELRs enables assembly into fibrillar aggregates. The interplay between the assembly of AMPs and ELRs provides an innovative molecular tool in the development of self-assembling nanosystems with potential use for biotechnological and biomedical applications.
Persistent Identifierhttp://hdl.handle.net/10722/318873
ISSN
2023 Impact Factor: 5.5
2023 SCImago Journal Rankings: 1.232
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorAcosta, Sergio-
dc.contributor.authorYe, Zhou-
dc.contributor.authorAparicio, Conrado-
dc.contributor.authorAlonso, Matilde-
dc.contributor.authorRodríguez-Cabello, José Carlos-
dc.date.accessioned2022-10-11T12:24:45Z-
dc.date.available2022-10-11T12:24:45Z-
dc.date.issued2020-
dc.identifier.citationBiomacromolecules, 2020, v. 21, n. 10, p. 4043-4052-
dc.identifier.issn1525-7797-
dc.identifier.urihttp://hdl.handle.net/10722/318873-
dc.description.abstractAntimicrobial peptides (AMPs) have attracted great interest as they constitute one of the most promising alternatives against drug-resistant infections. Their amphipathic nature not only provides them antimicrobial and immunomodulatory properties but also the ability to self-assemble into supramolecular nanostructures. Here, we propose their use as self-assembling domains to drive hierarchical organization of intrinsically disordered protein polymers (IDPPs). Using a modular approach, hybrid protein-engineered polymers were recombinantly produced, thus combining designer AMPs and a thermoresponsive IDPP, an elastin-like recombinamer (ELR). We exploited the ability of these AMPs and ELRs to self-assemble to develop supramolecular nanomaterials by way of a dual-assembly process. First, the AMPs trigger the formation of nanofibers; then, the thermoresponsiveness of the ELRs enables assembly into fibrillar aggregates. The interplay between the assembly of AMPs and ELRs provides an innovative molecular tool in the development of self-assembling nanosystems with potential use for biotechnological and biomedical applications.-
dc.languageeng-
dc.relation.ispartofBiomacromolecules-
dc.titleDual Self-Assembled Nanostructures from Intrinsically Disordered Protein Polymers with LCST Behavior and Antimicrobial Peptides-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1021/acs.biomac.0c00865-
dc.identifier.pmid32786727-
dc.identifier.scopuseid_2-s2.0-85092803236-
dc.identifier.volume21-
dc.identifier.issue10-
dc.identifier.spage4043-
dc.identifier.epage4052-
dc.identifier.eissn1526-4602-
dc.identifier.isiWOS:000580890000008-

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