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- Publisher Website: 10.1021/acs.biomac.0c00865
- Scopus: eid_2-s2.0-85092803236
- PMID: 32786727
- WOS: WOS:000580890000008
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Article: Dual Self-Assembled Nanostructures from Intrinsically Disordered Protein Polymers with LCST Behavior and Antimicrobial Peptides
Title | Dual Self-Assembled Nanostructures from Intrinsically Disordered Protein Polymers with LCST Behavior and Antimicrobial Peptides |
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Authors | |
Issue Date | 2020 |
Citation | Biomacromolecules, 2020, v. 21, n. 10, p. 4043-4052 How to Cite? |
Abstract | Antimicrobial 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 Identifier | http://hdl.handle.net/10722/318873 |
ISSN | 2023 Impact Factor: 5.5 2023 SCImago Journal Rankings: 1.232 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Acosta, Sergio | - |
dc.contributor.author | Ye, Zhou | - |
dc.contributor.author | Aparicio, Conrado | - |
dc.contributor.author | Alonso, Matilde | - |
dc.contributor.author | Rodríguez-Cabello, José Carlos | - |
dc.date.accessioned | 2022-10-11T12:24:45Z | - |
dc.date.available | 2022-10-11T12:24:45Z | - |
dc.date.issued | 2020 | - |
dc.identifier.citation | Biomacromolecules, 2020, v. 21, n. 10, p. 4043-4052 | - |
dc.identifier.issn | 1525-7797 | - |
dc.identifier.uri | http://hdl.handle.net/10722/318873 | - |
dc.description.abstract | Antimicrobial 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.language | eng | - |
dc.relation.ispartof | Biomacromolecules | - |
dc.title | Dual Self-Assembled Nanostructures from Intrinsically Disordered Protein Polymers with LCST Behavior and Antimicrobial Peptides | - |
dc.type | Article | - |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1021/acs.biomac.0c00865 | - |
dc.identifier.pmid | 32786727 | - |
dc.identifier.scopus | eid_2-s2.0-85092803236 | - |
dc.identifier.volume | 21 | - |
dc.identifier.issue | 10 | - |
dc.identifier.spage | 4043 | - |
dc.identifier.epage | 4052 | - |
dc.identifier.eissn | 1526-4602 | - |
dc.identifier.isi | WOS:000580890000008 | - |