Development of Oxadiazolone Activity-Based Probes Targeting FphE for Specific Detection of Staphylococcus aureus Infections.
Jeyun JoTulsi UpadhyayEmily C WoodsKi Wan ParkNichole J PedowitzJoanna Jaworek-KorjakowskaSijie WangTulio A ValdezMatthias FellnerMatthew M BogyoPublished in: Journal of the American Chemical Society (2024)
Staphylococcus aureus ( S. aureus ) is a major human pathogen that is responsible for a wide range of systemic infections. Since its propensity to form biofilms in vivo poses formidable challenges for both detection and treatment, tools that can be used to specifically image S. aureus biofilms are highly valuable for clinical management. Here, we describe the development of oxadiazolone-based activity-based probes to target the S. aureus -specific serine hydrolase FphE. Because this enzyme lacks homologues in other bacteria, it is an ideal target for selective imaging of S. aureus infections. Using X-ray crystallography, direct cell labeling, and mouse models of infection, we demonstrate that oxadiazolone-based probes enable specific labeling of S. aureus bacteria through the direct covalent modification of the FphE active site serine. These results demonstrate the utility of the oxadizolone electrophile for activity-based probes and validate FphE as a target for the development of imaging contrast agents for the rapid detection of S. aureus infections.
Keyphrases
- staphylococcus aureus
- fluorescence imaging
- small molecule
- high resolution
- living cells
- single molecule
- candida albicans
- mouse model
- endothelial cells
- biofilm formation
- loop mediated isothermal amplification
- nucleic acid
- real time pcr
- cancer therapy
- label free
- cystic fibrosis
- pseudomonas aeruginosa
- escherichia coli
- cell therapy
- magnetic resonance imaging
- mass spectrometry
- mesenchymal stem cells
- replacement therapy
- methicillin resistant staphylococcus aureus