Photocatalytic Degradation of Bacterial Lipopolysaccharides by Peptide-Coated TiO2 Nanoparticles
(2024) In ACS Applied Materials and Interfaces 16(44). p.60056-60069- Abstract
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 TiO2 nanoparticles (TiO2 NPs). While bare TiO2 NPs displayed minor binding to both LPS and LTA, coating TiO2 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 TiO2 NPs; hence, UV illumination triggered pronounced degradation of LPS and LTA by peptide-coated TiO2 NPs. Structural consequences of oxidative degradation... (More)
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 TiO2 nanoparticles (TiO2 NPs). While bare TiO2 NPs displayed minor binding to both LPS and LTA, coating TiO2 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 TiO2 NPs; hence, UV illumination triggered pronounced degradation of LPS and LTA by peptide-coated TiO2 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-TiO2 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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- author
- Caselli, Lucrezia LU ; Du, Guanqun LU ; Micciulla, Samantha ; Traini, Tanja ; Sebastiani, Federica LU ; Diedrichsen, Ragna Guldsmed ; Köhler, Sebastian LU ; Skoda, Maximilian W.A. ; van der Plas, Mariena J.A. LU and Malmsten, Martin LU
- organization
- publishing date
- 2024-11-06
- type
- Contribution to journal
- publication status
- published
- subject
- keywords
- antimicrobial peptide, lipopolysaccharide, oxidation, photocatalysis, TiO
- in
- ACS Applied Materials and Interfaces
- volume
- 16
- issue
- 44
- pages
- 14 pages
- publisher
- The American Chemical Society (ACS)
- external identifiers
-
- scopus:85207537877
- pmid:39443826
- ISSN
- 1944-8244
- DOI
- 10.1021/acsami.4c15706
- language
- English
- LU publication?
- yes
- additional info
- Publisher Copyright: © 2024 The Authors. Published by American Chemical Society.
- id
- 53633887-3e23-4f34-8dfd-03a14947da8e
- date added to LUP
- 2024-12-17 11:20:38
- date last changed
- 2025-07-16 17:12:50
@article{53633887-3e23-4f34-8dfd-03a14947da8e, abstract = {{<p>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<sub>2</sub> nanoparticles (TiO<sub>2</sub> NPs). While bare TiO<sub>2</sub> NPs displayed minor binding to both LPS and LTA, coating TiO<sub>2</sub> 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<sub>2</sub> NPs; hence, UV illumination triggered pronounced degradation of LPS and LTA by peptide-coated TiO<sub>2</sub> 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<sub>2</sub> 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.</p>}}, author = {{Caselli, Lucrezia and Du, Guanqun and Micciulla, Samantha and Traini, Tanja and Sebastiani, Federica and Diedrichsen, Ragna Guldsmed and Köhler, Sebastian and Skoda, Maximilian W.A. and van der Plas, Mariena J.A. and Malmsten, Martin}}, issn = {{1944-8244}}, keywords = {{antimicrobial peptide; lipopolysaccharide; oxidation; photocatalysis; TiO}}, language = {{eng}}, month = {{11}}, number = {{44}}, pages = {{60056--60069}}, publisher = {{The American Chemical Society (ACS)}}, series = {{ACS Applied Materials and Interfaces}}, title = {{Photocatalytic Degradation of Bacterial Lipopolysaccharides by Peptide-Coated TiO<sub>2</sub> Nanoparticles}}, url = {{http://dx.doi.org/10.1021/acsami.4c15706}}, doi = {{10.1021/acsami.4c15706}}, volume = {{16}}, year = {{2024}}, }