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

Sergio Acosta, Zhou Ye, Conrado Aparicio, Matilde Alonso, José Carlos Rodríguez-Cabello

Research output: Contribution to journalArticlepeer-review

16 Scopus citations

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.

Original languageEnglish (US)
Pages (from-to)4043-4052
Number of pages10
JournalBiomacromolecules
Volume21
Issue number10
DOIs
StatePublished - Oct 12 2020

Bibliographical note

Publisher Copyright:
Copyright © 2020 American Chemical Society.

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