New ethionamide boosters and EthR2: structural and energetic analysis
| Autor: | A. H. Lima Costa, Valder N. Freire, J. I. N. Oliveira, J. F. Vianna, Umberto L. Fulco, E. D. Barbosa, Katyanna S Bezerra, J. X. Lima Neto |
|---|---|
| Rok vydání: | 2021 |
| Předmět: |
Stereochemistry
Protein Data Bank (RCSB PDB) Antitubercular Agents General Physics and Astronomy Repressor Conjugated system Molecular Dynamics Simulation Ligands Mycobacterium tuberculosis medicine Humans Tuberculosis Physical and Theoretical Chemistry Binding site Ethionamide Density Functional Theory Binding Sites biology Chemistry Monooxygenase biology.organism_classification In vitro Repressor Proteins medicine.drug |
| Zdroj: | Physical chemistry chemical physics : PCCP. 23(40) |
| ISSN: | 1463-9084 |
| Popis: | Ethionamide (ETH) is a high-profile drug for the treatment of patients with multidrug-resistant Mycobacterium tuberculosis and, in order to produce its inhibitory effects, it needs to be bioactivated by monooxygenase EthA. This process is under the control of the transcriptional repressors EthR and EthR2, so that their inhibition results in the boosting of ethionamide activation. Herein, through crystallographic data and computer simulations, we calculated the interaction binding energies of four inhibitors with improved in vitro potency, namely BDM76060 (PDB ID: 6HS1), BDM72201 (PDB ID: 6HRX), BDM76150 (PDB ID: 6HS2) and BDM72719 (PDB ID: 6HRY), in complexes with the transcriptional repressor EthR2, using density functional theory (DFT) within the molecular fractionation with conjugated caps (MFCC) approach. It was observed that these ligands share the same binding site within a 10.0 A radius of the EthR2 protein; however, their structural particularities have a significant impact on the global energies of systems. The BDM72201 and BDM72719 components are weakly attached to the binding site, while BDM76060 and BDM76150 components produce stronger bonds, corroborating with experimental studies demonstrating that BDM76060 and BDM76150 are more successful in producing inhibitory effects. BDM76060 and BDM76150 have many functional groups that increase the contact surface with the protein and attract a more significant number of amino acid residues, being able to produce polarities that generate stronger interactions. In the current scenario of a growing number of cases of bacterial resistance, the obtained data can be used to guide clinical trials of these inhibitors and other inhibitors that act on the alternative EthR2 pathway, focusing on improving the activity of ethionamide, its effectiveness, a reduction in the treatment time and exposure to cytotoxic effects. |
| Databáze: | OpenAIRE |
| Externí odkaz: |
|