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J Biol Chem ; 280(48): 39709-15, 2005 Dec 02.
Article in English | MEDLINE | ID: mdl-16174771

ABSTRACT

The continuous emergence of antibiotic resistance demands that novel classes of antibiotics continue to be developed. The division machinery of bacteria is an attractive target because it comprises seven or more essential proteins that are conserved almost throughout the bacteria but are absent from humans. We describe the development of a cell-based assay for inhibitors of cell division and its use to isolate a new inhibitor of FtsZ protein, a key player in the division machinery. Biochemical, cytological, and genetic data are presented that demonstrate that FtsZ is the specific target for the compound. We also describe the effects of more potent analogues of the original hit compound that act on important pathogens, again at the level of cell division. The assay and the compounds have the potential to provide novel antibiotics with no pool of pre-existing resistance. They have provided new insight into cytokinesis in bacteria and offer important reagents for further studies of the cell division machinery.


Subject(s)
Anti-Infective Agents/pharmacology , Cytokinesis/drug effects , Drug Resistance, Bacterial , Microbial Sensitivity Tests/methods , Phenyl Ethers/pharmacology , beta-Alanine/analogs & derivatives , Bacillus subtilis , Bacterial Proteins/metabolism , Cell Division , Cloning, Molecular , Cytoskeletal Proteins/metabolism , Dose-Response Relationship, Drug , GTP Phosphohydrolases/metabolism , Genes, Reporter , Green Fluorescent Proteins , Models, Molecular , Mutation , Phenotype , Temperature , Time Factors , beta-Alanine/pharmacology
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