表面改性
肽
化学
抗菌剂
组合化学
圆二色性
碳二亚胺
共价键
抗菌肽
部分
有机化学
立体化学
生物化学
物理化学
作者
Adailson Pereira de Souza,K.R. de Souza,Dario L. Santos,Daniel A. G. R. Michel,Poliana Ribeiro Barroso,Kelly Cristina Kato,Helen Rodrigues Martins,Antonio Flavio Aires Rodrigues,Jarbas M. Resende,João Paulo de Mesquita,Rodrigo M. Verly
标识
DOI:10.1016/j.matchemphys.2023.128101
摘要
The synthesis of nanobiostructures ([email protected]) composed of carbon dots (CD) covalently bound to the antimicrobial peptide ecPis-4s is reported. Nanoparticle functionalization was achieved by pre-activating the oxygenated functional groups using 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide (EDAC) and ethyl (hydroxyimino)cyanoacetate in an aqueous medium. The obtained nanobiostructures were characterized by several techniques, including FTIR and 1H NMR spectroscopies. The functionalization does not compromise the optical properties of CD. The polypeptide moiety of the peptide-decorated nanoparticles retains the active α-helical conformation and lytic activity in the presence of anionic phospholipid vesicles as observed in the circular dichroism and calcein release experiments. Consequently, the [email protected] nanobiostructures present similar activity against Gram-positive (S. aureus and S. agalactiae) and Gram-negative (E. coli and P. aeruginosa) bacteria strains when compared to the free peptide. To our knowledge, this is the first report on carbon dots containing a covalently bound antimicrobial peptide. Thereby, in an era of increasing antimicrobial resistance, the synthesis and investigations performed in this work led to materials with potential for monitoring, in loco, bacterial contamination via exposure to UV radiation.
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