Antimicrobial Peptide Coating of TiO 2 Nanoparticles for Boosted Antimicrobial Effects
Source abstract
Abstract
Abstract This study explores the coating of photocatalytic nanoparticles with antimicrobial peptides (AMPs) for boosted antimicrobial effects, and how such effects depend on AMP properties. For this, TiO 2 nanoparticles are coated with the AMP KYE21 or its hydrophobically enhanced variant WWWKYE21. Mirroring effects of free peptides, coated nanoparticles displayed higher binding and UV‐induced degradation for bacteria‐like than for mammalian‐like membranes. In addition, they degraded bacterial lipopolysaccharides (LPS). WWWKYE21‐coated nanoparticles displayed higher binding to LPS and bacteria‐like membranes and photocatalytic degradation, although saturation effects are found at high nanoparticle binding. Neutron reflectometry showed that binding of peptide‐coated nanoparticles to bacteria‐like membranes resulted in partial lipid removal in the absence of UV, but that UV illumination caused additional degradation, featuring increases in the hydration of headgroup and acyl chain regions. For LPS, UV induced removal of its outer O‐antigen region. Analogous to findings in model systems, antimicrobial effects of peptide‐coated nanoparticles against Escherichia coli bacteria on illumination are pronounced, while toxicity against human monocytes remained low. Altogether, results show that AMP coating boosts the antimicrobial effects of photocatalytic nanoparticles without causing cell toxicity. From a broader perspective, the study points to the potential of nanoarchitectonic combination of component properties for the design of composite NP properties.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Antimicrobial Peptides and Activities · Polydiacetylene-based materials and applications · Silk-based biomaterials and applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Physical Chemistry Lund University Lund SE‐22100 Sweden
Department of Pharmacy University of Copenhagen Copenhagen DK‐2100 Denmark
Institut Laue–Langevin CS 20156 Grenoble 38042 Cedex 9 France
LINXS Institute for Advanced Neutron and X‐ray Science Scheelevagen 19 Lund 22370 Sweden
ISIS Pulsed Neutron and Muon Source Rutherford Appleton Laboratory Harwell OX11 0QX UK
Funding
Vetenskapsrådet · Danmarks Frie Forskningsfond · ISIS Neutron and Muon Source
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