| Title: |
Antibacterial and Anti-Inflammatory Activity of Branched Peptides Derived from Natural Host Defense Sequences |
| Authors: |
Meogrossi, Giada; Tollapi, Eva; Rencinai, Alessandro; Brunetti, Jlenia; Scali, Silvia; Paccagnini, Eugenio; Gentile, Mariangela; Lupetti, Pietro; Pollini, Simona; Rossolini, Gian Maria; Bernini, Andrea; Pini, Alessandro; Bracci, Luisa; Falciani, Chiara |
| Contributors: |
Meogrossi, Giada; Tollapi, Eva; Rencinai, Alessandro; Brunetti, Jlenia; Scali, Silvia; Paccagnini, Eugenio; Gentile, Mariangela; Lupetti, Pietro; Pollini, Simona; Rossolini, Gian Maria; Bernini, Andrea; Pini, Alessandro; Bracci, Luisa; Falciani, Chiara |
| Publication Year: |
2024 |
| Collection: |
Università degli Studi di Siena: USiena air |
| Subject Terms: |
Animals; Anti-Bacterial Agents; Anti-Inflammatory Agents; Antimicrobial Cationic Peptides; Antimicrobial Peptides; Biofilms; Escherichia coli; Human; Mice; Microbial Sensitivity Tests |
| Description: |
Antibiotic resistance is a major global health threat, necessitating the development of new treatments and diverse molecules to combat severe infections and preserve the efficacy of existing drugs. Antimicrobial peptides (AMPs) offer a versatile arsenal against bacteria, and peptide structure branching can enhance their resistance to proteases and improve their overall efficacy. A small library of peptides derived from natural host defense peptides and synthesized in a tetrabranched form was selected against E. coli. Six selected branched peptides were further studied for antibacterial activity against a panel of strains, biofilm inhibition, protease resistance, and cytotoxicity. Their structure was predicted computationally and their mechanism of action was investigated by electron microscopy and by using fluorescent dyes. The peptide BAMP2 showed promise in a mouse skin infection model, indicating the potential for local infection treatment. |
| Document Type: |
article in journal/newspaper |
| File Description: |
STAMPA |
| Language: |
English |
| Relation: |
info:eu-repo/semantics/altIdentifier/pmid/39260445; info:eu-repo/semantics/altIdentifier/wos/WOS:001311398100001; volume:67; issue:18; firstpage:16145; lastpage:16156; numberofpages:12; journal:JOURNAL OF MEDICINAL CHEMISTRY; https://hdl.handle.net/11365/1274797; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11440494/ |
| DOI: |
10.1021/acs.jmedchem.4c00810 |
| Availability: |
https://hdl.handle.net/11365/1274797; https://doi.org/10.1021/acs.jmedchem.4c00810; https://pubs.acs.org/doi/10.1021/acs.jmedchem.4c00810; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11440494/ |
| Rights: |
info:eu-repo/semantics/openAccess |
| Accession Number: |
edsbas.AC7B233A |
| Database: |
BASE |