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Variations in the Binding Pocket of an Inhibitor of the Bacterial Division Protein FtsZ across Genotypes and Species

By Amanda Miguel (712748), Jen Hsin (230213), Tianyun Liu (59361), Grace Tang (712749), Russ B. Altman (6158) and Kerwyn Casey Huang (73349)

Abstract

<div><p>The recent increase in antibiotic resistance in pathogenic bacteria calls for new approaches to drug-target selection and drug development. Targeting the mechanisms of action of proteins involved in bacterial cell division bypasses problems associated with increasingly ineffective variants of older antibiotics; to this end, the essential bacterial cytoskeletal protein FtsZ is a promising target. Recent work on its allosteric inhibitor, PC190723, revealed <i>in vitro</i> activity on <i>Staphylococcus aureus</i> FtsZ and <i>in vivo</i> antimicrobial activities. However, the mechanism of drug action and its effect on FtsZ in other bacterial species are unclear. Here, we examine the structural environment of the PC190723 binding pocket using PocketFEATURE, a statistical method that scores the similarity between pairs of small-molecule binding sites based on 3D structure information about the local microenvironment, and molecular dynamics (MD) simulations. We observed that species and nucleotide-binding state have significant impacts on the structural properties of the binding site, with substantially disparate microenvironments for bacterial species not from the <i>Staphylococcus</i> genus. Based on PocketFEATURE analysis of MD simulations of <i>S</i>. <i>aureus</i> FtsZ bound to GTP or with mutations that are known to confer PC190723 resistance, we predict that PC190723 strongly prefers to bind <i>Staphylococcus</i> FtsZ in the nucleotide-bound state. Furthermore, MD simulations of an FtsZ dimer indicated that polymerization may enhance PC190723 binding. Taken together, our results demonstrate that a drug-binding pocket can vary significantly across species, genetic perturbations, and in different polymerization states, yielding important information for the further development of FtsZ inhibitors.</p></div

Topics: Biological Sciences, cytoskeletal protein FtsZ, cell division bypasses problems, PC 190723 binding, 3 D structure information, vivo antimicrobial activities, gtp, bind Staphylococcus FtsZ, Bacterial Division Protein FtsZ, MD simulations, Staphylococcus aureus FtsZ, PC 190723 resistance, PC 190723 binding pocket, species
Year: 2015
DOI identifier: 10.1371/journal.pcbi.1004117
OAI identifier: oai:figshare.com:article/1356550
Provided by: FigShare
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