<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Ferreira CS</submitter><funding>Université de Strasbourg the Agence Nationale de la Recherche '</funding><funding>Coordenação de Aperfeiçoamento de Pessoal de Nível Superior-CAPES</funding><funding>Fundação de Amparo à Pesquisa de Minas Gerais-FAPEMIG</funding><funding>Conselho Nacional de Desenvolvimento Científico e Tecnológico-CNPq</funding><funding>LabEx Chemistry of Complex Systems</funding><funding>Foundation Jean-Marie Lehn/Interdisciplinary Thematic Institute SysChem/IdExUnistra</funding><pagination>952</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12299903</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>18(7)</volume><pubmed_abstract>&lt;b>Background/Objectives:&lt;/b> The increasing prevalence of multidrug-resistant bacteria presents a major global health challenge, prompting a search for innovative antimicrobial strategies. This study aimed to develop and evaluate a novel nanobiostructure combining alumina nanoparticles (NPs) with the antimicrobial peptide lunatin-1 (Lun-1), forming peptide-functionalized nanofilaments. The main objective was to investigate how the site of peptide functionalization (C-terminal vs. N-terminal) affects membrane interactions and antibacterial activity. &lt;b>Methods&lt;/b>: NP-peptide conjugates were synthesized via covalent bonding between lun-1 and alumina NP and characterized using transmission electron microscopy (TEM), X-ray diffraction (XRD), zeta potential analysis, dynamic light scattering </pubmed_abstract><journal>Pharmaceuticals (Basel, Switzerland)</journal><pubmed_title>Influence of Peptide Conjugation Sites on Lunatin-Alumina Nanoparticles: Implications for Membrane Interaction and Antimicrobial Activity.</pubmed_title><pmcid>PMC12299903</pmcid><funding_grant_id>CAPES- COFECUB program 88881.879071/2023-01</funding_grant_id><funding_grant_id>ANR-10-IDEX-0002</funding_grant_id><funding_grant_id>10-LABX-0026_CSC</funding_grant_id><funding_grant_id>438054/2018-0</funding_grant_id><funding_grant_id>APQ-02238-17</funding_grant_id><funding_grant_id>RED-00185-23</funding_grant_id><funding_grant_id>projects Naturalarsenal 19-AMRB-0004-02, AmphiPep 20-CE18-0021, and SAFEST 21-CE18-0043)</funding_grant_id><pubmed_authors>Nunes LO</pubmed_authors><pubmed_authors>Salnikov ES</pubmed_authors><pubmed_authors>Bechinger B</pubmed_authors><pubmed_authors>Verly RM</pubmed_authors><pubmed_authors>Kato KC</pubmed_authors><pubmed_authors>Ferreira CS</pubmed_authors><pubmed_authors>Costa LMF</pubmed_authors><pubmed_authors>de Souza KR</pubmed_authors><pubmed_authors>de Castro Pimenta AM</pubmed_authors><pubmed_authors>Araujo GP</pubmed_authors><pubmed_authors>Resende JM</pubmed_authors><pubmed_authors>Martins HR</pubmed_authors></additional><is_claimable>false</is_claimable><name>Influence of Peptide Conjugation Sites on Lunatin-Alumina Nanoparticles: Implications for Membrane Interaction and Antimicrobial Activity.</name><description>&lt;b>Background/Objectives:&lt;/b> The increasing prevalence of multidrug-resistant bacteria presents a major global health challenge, prompting a search for innovative antimicrobial strategies. This study aimed to develop and evaluate a novel nanobiostructure combining alumina nanoparticles (NPs) with the antimicrobial peptide lunatin-1 (Lun-1), forming peptide-functionalized nanofilaments. The main objective was to investigate how the site of peptide functionalization (C-terminal vs. N-terminal) affects membrane interactions and antibacterial activity. &lt;b>Methods&lt;/b>: NP-peptide conjugates were synthesized via covalent bonding between lun-1 and alumina NP and characterized using transmission electron microscopy (TEM), X-ray diffraction (XRD), zeta potential analysis, dynamic light scattering </description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Jun</publication><modification>2025-08-13T03:04:44.249Z</modification><creation>2025-08-13T03:04:44.249Z</creation></dates><accession>S-EPMC12299903</accession><cross_references><pubmed>40732243</pubmed><doi>10.3390/ph18070952</doi></cross_references></HashMap>