Identification of covalent inhibitors of Staphylococcus aureus serine hydrolases important for virulence and biofilm formation

Staphylococcus aureus is a leading cause of bacteria-associated mortality worldwide. New tools are needed to both image and treat this pathogen. We previously identified a group of S. aureus serine hydrolases (Fphs), which regulate aspects of virulence and lipid metabolism. However, due to high structural and functional similarities, it remains challenging to distinguish the specific roles of members of this family. Here, we apply a high-throughput screening approach using a library of covalent electrophiles to identify inhibitors for FphB, FphE, and FphH. We identify selective covalent inhibitors for each target without the need for extensive medicinal chemistry optimization. Structural and biochemical analysis identify novel binding modes for several of the inhibitors. Functional studies using the inhibitors suggest that all three hydrolases likely play distinct functional roles in biofilm formation and virulence. This approach has the potential to be applied to target hydrolases in other diverse pathogens or higher eukaryotes.

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Publication Details

Journal
Nature Communications
Published
2025-05-30
DOI
https://doi.org/10.1038/s41467-025-60367-3
Citations
6
Primary Topic
Click Chemistry and Applications
Type
article
Field-Weighted Citation Impact
5.62

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article

Identification of covalent inhibitors of Staphylococcus aureus serine hydrolases important for virulence and biofilm formation

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6 citations
Nature Communications
Click Chemistry and Applications
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article

Identification of covalent inhibitors of Staphylococcus aureus serine hydrolases important for virulence and biofilm formation

Nichole J. Pedowitz, Matthew S. Bogyo, Kjersti Julin, Jeyun Jo, Emily C. Woods, Marijn J. Hollander, Stephen Dela Ahator, Daniel Abegg, Christian S. Lentz, Franco F. Faucher, Md Jalal Uddin, Alexander Adibekian, Matthias Fellner, Ifeanyichukwu E. Eke, Tulsi Upadhyay, Shiyu Chen, Sijie Wang, John M. Bennett, Isabella Hammond
article en
6 citations

Abstract

Staphylococcus aureus is a leading cause of bacteria-associated mortality worldwide. New tools are needed to both image and treat this pathogen. We previously identified a group of S. aureus serine hydrolases (Fphs), which regulate aspects of virulence and lipid metabolism. However, due to high structural and functional similarities, it remains challenging to distinguish the specific roles of members of this family. Here, we apply a high-throughput screening approach using a library of covalent electrophiles to identify inhibitors for FphB, FphE, and FphH. We identify selective covalent inhibitors for each target without the need for extensive medicinal chemistry optimization. Structural and biochemical analysis identify novel binding modes for several of the inhibitors. Functional studies using the inhibitors suggest that all three hydrolases likely play distinct functional roles in biofilm formation and virulence. This approach has the potential to be applied to target hydrolases in other diverse pathogens or higher eukaryotes.

Nature CommunicationsVol. 16(1)
University of Illinois Chicago (US), Stanford Medicine (US), UiT The Arctic University of Norway (NO), University of Otago (NZ), Stanford University (US)
National Science Foundation, Australian Nuclear Science and Technology Organisation, Australian Synchrotron, Fundación Bancaria Caixa d'Estalvis i Pensions de Barcelona, National Institutes of Health, Genentech, Chemistry, Engineering and Medicine for Human Health, Stanford University, Health Research Council of New Zealand, Marsden Fund
Openalex Percentile: Top 4%
Click Chemistry and Applications
5.62
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