ACS Applied Materials & Interfaces · 2024 · 14 citations · 49 references
Natural SciencesMaterials ScienceMicrobiologyBiocatalysisBiomaterialsSurface ScienceAntimicrobial BiomaterialsAntimicrobial PeptidesBio-based MaterialsOxidative Damage To BiomoleculesPeptide ChemistryPhotocatalysisAntibacterial PeptidesAntimicrobial Peptide ActivityLipopolysaccharide-induced DamageNeutron ReflectometryPeptide CoatingsPhotocatalytic DegradationPhotocatalytic TreatmentReactive Oxygen Species Generation
High Resolution Image Download MS PowerPoint Slide In this study, we report the degradation of smooth and rough lipopolysaccharides (LPS) from Gram-negative bacteria and of lipoteichoic acid (LTA) from Gram-positive bacteria by peptide-coated TiO 2 nanoparticles (TiO 2 NPs). While bare TiO 2 NPs displayed minor binding to both LPS and LTA, coating TiO 2 NPs with the antimicrobial peptide LL-37 dramatically increased the level of binding to both LPS and LTA, decorating these uniformly. Importantly, peptide coating did not suppress reactive oxygen species generation of TiO 2 NPs; hence, UV illumination triggered pronounced degradation of LPS and LTA by peptide-coated TiO 2 NPs. Structural consequences of oxidative degradation were examined by neutron reflectometry for smooth LPS, showing that degradation occurred preferentially in its outer O-antigen tails. Furthermore, cryo-TEM and light scattering showed lipopolysaccharide fragments resulting from degradation to be captured by the NP/lipopolysaccharide coaggregates. The capacity of LL-37-TiO 2 NPs to capture and degrade LPS and LTA was demonstrated to be of importance for their ability to suppress lipopolysaccharide-induced activation in human monocytes at simultaneously low toxicity. Together, these results suggest that peptide-coated photocatalytic NPs offer opportunities for the confinement of infection and inflammation.
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NIH Image to ImageJ: 25 years of image analysis
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