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Carbamoyl-phosphate synthase 1 as a novel target of phomoxanthone a, a bioactive fungal metabolite
- Source :
- Biomolecules, Vol 10, Iss 846, p 846 (2020), Biomolecules, Volume 10, Issue 6
- Publication Year :
- 2020
-
Abstract
- Phomoxanthone A, a bioactive xanthone dimer isolated from the endophytic fungus Phomopsis sp., is a mitochondrial toxin weakening cellular respiration and electron transport chain activity by a fast breakup of the mitochondrial assembly. Here, a multi-disciplinary strategy has been developed and applied for identifying phomoxanthone A target(s) to fully address its mechanism of action, based on drug affinity response target stability and targeted limited proteolysis. Both approaches point to the identification of carbamoyl-phosphate synthase 1 as a major phomoxanthone A target in mitochondria cell lysates, giving also detailed insights into the ligand/target interaction sites by molecular docking and assessing an interesting phomoxanthone A stimulating activity on carbamoyl-phosphate synthase 1. Thus, phomoxanthone A can be regarded as an inspiring molecule for the development of new leads in counteracting hyperammonemia states.
- Subjects :
- Proteomics
Bioactive xanthone
Cellular respiration
Proteolysis
Xanthones
Carbamoyl-Phosphate Synthase (Ammonia)
lcsh:QR1-502
Phomopsis
Targeted-limited proteolysis
Mitochondrion
010402 general chemistry
01 natural sciences
Biochemistry
Article
lcsh:Microbiology
03 medical and health sciences
chemistry.chemical_compound
Xanthone
medicine
Humans
Drug affinity responsive target stability
Molecular docking
Molecular Biology
030304 developmental biology
0303 health sciences
medicine.diagnostic_test
ATP synthase
biology
Chemistry
Ligand (biochemistry)
Electron transport chain
0104 chemical sciences
Molecular Docking Simulation
Mechanism of action
biology.protein
medicine.symptom
HeLa Cells
Subjects
Details
- Language :
- English
- Database :
- OpenAIRE
- Journal :
- Biomolecules, Vol 10, Iss 846, p 846 (2020), Biomolecules, Volume 10, Issue 6
- Accession number :
- edsair.doi.dedup.....330fb1a6538cf580c02aaa66bb1412b1