Novel inhibitors of bacterial cytokinesis identified by a cell-based antibiotic screening assay

被引:97
作者
Stokes, NR
Sievers, J
Barker, S
Bennett, JM
Brown, DR
Collins, I
Errington, VM
Foulger, D
Hall, M
Halsey, R
Johnson, H
Rose, V
Thomaides, HB
Haydon, DJ
Czaplewski, LG
Errington, J
机构
[1] Univ Oxford, Prolysis Ltd, Yarnton OX5 1PF, Oxon, England
[2] Univ Oxford, Sir William Dunn Sch Pathol, Oxford OX1 3RE, England
基金
英国医学研究理事会;
关键词
D O I
10.1074/jbc.M506741200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:39709 / 39715
页数:7
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