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Inhibition of Peroxidase Activity of Cytochrome c: De Novo Compound Discovery and Validation.
- Source :
-
Molecular pharmacology [Mol Pharmacol] 2015 Sep; Vol. 88 (3), pp. 421-7. Date of Electronic Publication: 2015 Jun 15. - Publication Year :
- 2015
-
Abstract
- Cytochrome c (cyt c) release from mitochondria is accepted to be the point of no return for eliciting a cascade of interactions that lead to apoptosis. A strategy for containing sustained apoptosis is to reduce the mitochondrial permeability pore opening. Pore opening is enhanced by peroxidase activity of cyt c gained upon its complexation with cardiolipin in the presence of reactive oxygen species. Blocking access to the heme group has been proposed as an effective intervention method for reducing, if not eliminating, the peroxidase activity of cyt c. In the present study, using a combination of druggability simulations, pharmacophore modeling, virtual screening, and in vitro fluorescence measurements to probe peroxidase activity, we identified three repurposable drugs and seven compounds that are validated to effectively inhibit the peroxidase activity of cyt c.<br /> (Copyright © 2015 by The American Society for Pharmacology and Experimental Therapeutics.)
- Subjects :
- Amino Acid Sequence
Electron Transport Complex IV antagonists & inhibitors
Enzyme Inhibitors pharmacology
Humans
Molecular Docking Simulation
Molecular Sequence Data
Peroxidases chemistry
Small Molecule Libraries pharmacology
Catalytic Domain
Electron Transport Complex IV chemistry
Enzyme Inhibitors chemistry
Peroxidases antagonists & inhibitors
Small Molecule Libraries chemistry
Subjects
Details
- Language :
- English
- ISSN :
- 1521-0111
- Volume :
- 88
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Molecular pharmacology
- Publication Type :
- Academic Journal
- Accession number :
- 26078313
- Full Text :
- https://doi.org/10.1124/mol.115.097816