8EXD

Crystal structure of Aspergillus fumigatus sterylglucosidase A

Summary for 8EXD

• Entry DOI: 10.2210/pdb8exd/pdb
• Descriptor: Sterylglucosidase A (SglA) (1 entity in total)
• Functional Keywords: glucosidase, sterylglucosidase, hydrolase
• Biological source: Aspergillus fumigatus Af293
• Total number of polymer chains: 4
• Total formula weight: 353313.75

Authors

Pereira de Sa, N.,Del Poeta, M.,Airola, M.V. (deposition date: 2022-10-25, release date: 2023-03-01, Last modification date: 2023-10-25)

Primary citation

Pereira de Sa, N.,Jayanetti, K.,Rendina, D.,Clement, T.,Soares Brauer, V.,Mota Fernandes, C.,Ojima, I.,Airola, M.V.,Del Poeta, M.
Targeting Sterylglucosidase A to Treat Aspergillus fumigatus Infections.
Mbio, 14:e0033923-e0033923, 2023

PubMed Abstract: Invasive fungal infections are a leading cause of death in immunocompromised patients. Current therapies have several limitations, and innovative antifungal agents are critically needed. Previously, we identified the fungus-specific enzyme sterylglucosidase as essential for pathogenesis and virulence of Cryptococcus neoformans and Aspergillus fumigatus () in murine models of mycoses. Here, we developed sterylglucosidase A (SglA) as a therapeutic target. We identified two selective inhibitors of SglA with distinct chemical scaffolds that bind in the active site of SglA. Both inhibitors induce sterylglucoside accumulation and delay filamentation in and increase survival in a murine model of pulmonary aspergillosis. Structure-activity relationship (SAR) studies identified a more potent derivative that enhances both phenotypes and survival. These findings support sterylglucosidase inhibition as a promising antifungal approach with broad-spectrum potential. Invasive fungal infections are a leading cause of death in immunocompromised patients. Aspergillus fumigatus is a fungus ubiquitously found in the environment that, upon inhalation, causes both acute and chronic illnesses in at-risk individuals. A. fumigatus is recognized as one of the critical fungal pathogens for which a substantive treatment breakthrough is urgently needed. Here, we studied a fungus-specific enzyme, sterylglucosidase A (SglA), as a therapeutic target. We identified selective inhibitors of SglA that induce accumulation of sterylglucosides and delay filamentation in A. fumigatus and increase survival in a murine model of pulmonary aspergillosis. We determined the structure of SglA, predicted the binding poses of these inhibitors through docking analysis, and identified a more efficacious derivative with a limited SAR study. These results open several exciting avenues for the research and development of a new class of antifungal agents targeting sterylglucosidases.

PubMed: 36877042
DOI: 10.1128/mbio.00339-23

Experimental method

X-RAY DIFFRACTION (3.8 Å)