التفاصيل البيبلوغرافية
| العنوان: |
Computational Mutagenesis and Inhibition of Staphylococcus aureus AgrA LytTR Domain Using Phenazine Scaffolds: Insight From a Biophysical Study. |
| المؤلفون: |
Manu, Prince, Nketia, Prisca Baah, Osei-Poku, Priscilla, Kwarteng, Alexander, Cantore, Stefania |
| المصدر: |
BioMed Research International; 9/17/2024, Vol. 2024, p1-15, 15p |
| مصطلحات موضوعية: |
ANTIBIOTICS, HETEROCYCLIC compounds, BACTERIAL proteins, COMPUTER-assisted molecular modeling, IN vitro studies, BINDING sites, STAPHYLOCOCCAL diseases, BIOFILMS, MICROBIAL virulence, BIOPHYSICS, BACTERIAL physiology, DRUG resistance in microorganisms, STAPHYLOCOCCUS aureus, DESCRIPTIVE statistics, GENETIC mutation, DRUG development, SCIENTIFIC method, BACTERIAL diseases |
| مستخلص: |
Biofilm formation by Staphylococcus aureus is a major challenge in clinical settings due to its role in persistent infections. The AgrA protein, a key regulator in biofilm development, is a promising target for therapeutic intervention. This study investigates the antibiofilm potential of halogenated phenazine compounds by targeting AgrA and explores their molecular interactions to provide insights for drug development. We employed molecular docking, molecular dynamics simulations, and computational mutagenesis to evaluate the binding of halogenated phenazine compounds (C1 to C7, HP, and HP‐14) to AgrA. Binding free energy analysis was performed to assess the affinity of these compounds for the AgrA‐DNA complex. Additionally, the impact of these compounds on AgrA's structural conformation and salt bridge interactions was examined. The binding‐free energy analysis revealed that all compounds enhance binding affinity compared to the Apo form of AgrA, which has a ΔGbind of −80.75 kcal/mol. The strongest binding affinities were observed with compounds C7 (−113.84 kcal/mol), HP‐14 (−115.23 kcal/mol), and HP (−112.28 kcal/mol), highlighting their effectiveness. Molecular dynamics simulations demonstrated that these compounds bind at the hydrophobic cleft of AgrA, disrupting essential salt bridge interactions between His174‐Glu163 and His174‐Glu226. This disruption led to structural conformational changes and reduced DNA binding affinity, aligning with experimental findings on biofilm inhibition. The halogenated phenazine compounds effectively inhibit biofilm formation by targeting AgrA, disrupting its DNA‐binding function. The study supports the potential of these compounds as antibiofilm agents and provides a foundation for rational drug design targeting the AgrA‐DNA interaction. Future research should focus on further optimizing these lead compounds and exploring additional active sites on AgrA to develop novel treatments for biofilm‐associated infections. [ABSTRACT FROM AUTHOR] |
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| قاعدة البيانات: |
Complementary Index |
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