Inspiration from cruzioseptin-1: membranolytic analogue with improved antibacterial properties

Peptide engineering has gained attraction as a source of new cationicity-enhanced analogues with high potential for the design of next-generation antibiotics. In this context, cruzioseptin-1 (CZS-1), a peptide identified from Cruziohyla calcarifer , is recognized for its antimicrobial potency. Howev...

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Veröffentlicht in:Amino acids 2023, Vol.55 (1), p.113-124
Hauptverfasser: Bermúdez-Puga, Sebastián, Morán-Marcillo, Giovanna, Espinosa de los Monteros-Silva, Nina, Naranjo, Renato E., Toscano, Fernanda, Vizuete, Karla, Torres Arias, Marbel, Almeida, José R., Proaño-Bolaños, Carolina
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Sprache:eng
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Zusammenfassung:Peptide engineering has gained attraction as a source of new cationicity-enhanced analogues with high potential for the design of next-generation antibiotics. In this context, cruzioseptin-1 (CZS-1), a peptide identified from Cruziohyla calcarifer , is recognized for its antimicrobial potency. However, this amidated-peptide is moderately hemolytic. In order to reduce toxicity and increase antimicrobial potency, 3 peptide analogues based on cruzioseptin-1 were designed and evaluated. [K4K15]CZS-1, an analogue with increased cationicity and reduced hydrophobicity, showed antibacterial, antifungal and antiproliferative properties. In addition, [K4K15]CZS-1 is less hemolytic than CZS-1. The in silico and scanning electron microscopy analysis reveal that [K4K15]CZS-1 induces a membranolytic effect on bacteria. Overall, these results confirm the potential of CZS-1 as source of inspiration for design new selective antimicrobial analogues useful for development of new therapeutic agents.
ISSN:0939-4451
1438-2199
DOI:10.1007/s00726-022-03209-6