Computer-aided identification of novel 3,5-substituted rhodanine derivatives with activity against Staphylococcus aureus DNA gyrase

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• 作者：Malela M. Werner^a ; Zhiyu Li^b ; Randy J. Zauhar^a ; ^{r.zauhar@usciences.edu" class="auth_mail}
• 关键词：PNP ; purine nucleoside phosphorylase ; MESG ; 2-amino-6-mercapto-7-methylpurine ribose ; GLIDE XP ; grid-based ligand docking with energetics extra-precision ; OPLS ; optimized potentials for liquid simulations ; SPC water ; simple point charge water ; NPT ensemble ; isothermal&ndash ; isobaric ensemble ; RMSD ; root&ndash ; mean&ndash ; square deviation ; #rtvFG ; number of reactive functional groups ; SASA ; total solvent accessible surface area (SASA) in square angstroms using a probe with a 1.4  ; Å ; radiu
• 刊名：Bioorganic and Medicinal Chemistry
• 出版年：1 April, 2014
• 年：2014
• 卷：22
• 期：7
• 页码：2176-2187
• 全文大小：2191 K

文摘

Methicillin resistant Staphylococcus aureus (MRSA) is among the major drug resistant bacteria that persist in both the community and clinical settings due to resistance to commonly used antimicrobials. This continues to fuel the need for novel compounds that are active against this organism. For this purpose we have targeted the type IIA bacterial topoisomerase, DNA gyrase, an essential enzyme involved in bacterial replication, through the ATP-dependent supercoiling of DNA. The virtual screening tool Shape Signatures was applied to screen a large database for agents with shape similar to Novobiocin, a known gyrase B inhibitor. The binding energetics of the top hits from this initial screen were further validated by molecular docking. Compounds with the highest score on available crystal structure of homologous DNA gyrase from Thermus thermophilus were selected. From this initial set of compounds, several rhodanine-substituted derivatives had the highest antimicrobial activity against S. aureus, as determined by minimal inhibitory concentration assays, with Novobiocin as the positive control. Further activity validation of the rhodanine compounds through biochemical assays confirmed their inhibition of both the supercoiling and the ATPase activity of DNA gyrase. Subsequent docking and molecular dynamics on the crystal structure of DNA gyrase from S. aureus when it became available, provides further rationalization of the observed biochemical activity and understanding of the receptor-ligand interactions. A regression model for MIC prediction against S. aureus is generated based on the current molecules studied as well as other rhodanines derivatives found in the literature.