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Synthesis and Biological Activity of Ultrashort Antimicrobial Peptides Bearing a Non‐Coded Amino Acid

Title: Synthesis and Biological Activity of Ultrashort Antimicrobial Peptides Bearing a Non‐Coded Amino Acid
Authors: Peggion, Cristina; Schivo, Andrea; Rotondo, Martina; Oancea, Simona; Popovici, Lucia‐Florina; Călin, Teodora; Mkrtchyan, Anna; Saghyan, Ashot; Hayriyan, Liana; Khachatryan, Emma; Formaggio, Fernando; Biondi, Barbara
Source: Journal of Peptide Science ; volume 31, issue 5 ; ISSN 1075-2617 1099-1387
Publisher Information: Wiley
Publication Year: 2025
Collection: Wiley Online Library (Open Access Articles via Crossref)
Description: Antimicrobial resistance represents a significant global health threat, prompting the exploration of alternative therapeutic strategies. Antimicrobial peptides (AMPs) and lipopeptides are promising candidates due to their unique ability to disrupt bacterial cell membranes through mechanisms distinct from conventional antibiotics. These peptides are typically enhanced by motifs involving cationic amino acids, positive charge, and aromatic residues. Additionally, the conjugation of acyl chains to the N‐terminus of AMPs has been shown to improve their antimicrobial activity and selectivity. However, the susceptibility of peptides to enzymatic degradation presents a major limitation. To address this, we investigated the incorporation of non‐coded amino acids (NCAAs) to enhance peptide stability. Specifically, we synthesized the NCAA 2‐amino‐3‐(1 H ‐imidazol‐1‐yl)propanoic acid [His*], producing both enantiomers with high yield and optical purity. We then designed various analogs of ultra‐short AMPs by inserting His* at specific positions, evaluating their antimicrobial properties with different acyl chain lengths (C16 and C12) at the N‐terminus and the C‐terminus. We were able to identify a very promising candidate for applications ( P8 ) characterized by resistance to proteolysis and enhanced biological effectiveness.
Document Type: article in journal/newspaper
Language: English
DOI: 10.1002/psc.70021
Availability: https://doi.org/10.1002/psc.70021; https://onlinelibrary.wiley.com/doi/pdf/10.1002/psc.70021
Rights: http://creativecommons.org/licenses/by/4.0/
Accession Number: edsbas.4D2CE7F1
Database: BASE