Antibacterial Activity of Membrane-Permeabilizing Bactericidal Cyclodextrin Derivatives
Year: 2021
Type: article
Abstract: High Resolution Image Download MS PowerPoint Slide Antimicrobial peptides that act by disrupting bacterial membranes are attractive agents for treating drug-resistant bacteria. This study investigates a membrane-disrupting peptide mimic made of a cyclic oligosaccharide cyclodextrin scaffold that can be chemically polyfunctionalized. An antibacterial functional group on the peptide was simplified to an alkylamino group that combines cationic and hydrophobic moieties, the former to interact with the anionic bacterial membrane and the latter with the membrane interior. The cyclodextrins equipped with eight alkylamino groups on the molecules using a poly-click reaction exhibited antibacterial activity against Gram-positive and Gram-negative bacteria, including drug-resistant pathogens such as carbapenem-resistant Enterobacteriaceae . Several lines of evidence showed that these agents disrupt bacterial membranes, leading to rapid bacterial cell death. The resulting membrane perturbation was directly visualized using high-speed atomic force microscopy imaging. In Gram-negative bacteria, the membrane-permeabilizing action of these derivatives allowed the entry of co-treated traditional antibiotics, which were then active against these bacteria.
Source: ACS Omega
Language: English
Subfield: Applied Microbiology and Biotechnology
Field: Immunology and Microbiology
Domain: Life Sciences
Open Access status: gold
Estimated APC paid: $1,250
Awards: Development and AFM observation of immobilized planar membranes with controlled orientation of membrane proteins and asymmetry of lipid membranes, Ultrafast Atomic Force Microscopy Imaging of Phase Transition Phenomena on Ice Surface by Machine Learning, Study of Catalytic Activity of Anatase TiO2 and its Nano-cluster Using Atomic Force Microscopy, G504011909, 生細胞膜分子動態を観る極限時空間分解能AFMの創成, Studies of antimicrobial oligosaccharides, Synthesis of beta-glucan mimic polymers and elucidation of the molecular structure required for the immunological activation, Structural dynamics of K+ channel imaged by high-speed atomic force microscopy, Supramolecular structure of photoreceptor proteins and the dynamic molecular mechanism on signal transduction
OpenAlex ID: W3213036717
