Antibacterial agents that inhibit two-component signal transduction systems

被引:105
作者
Barrett, JF
Goldschmidt, RM
Lawrence, LE
Foleno, B
Chen, R
Demers, JP
Johnson, S
Kanojia, R
Fernandez, J
Bernstein, J
Licata, L
Donetz, A
Huang, S
Hlasta, DJ
Macielag, MJ
Ohemeng, K
Frechette, R
Frosco, MB
Klaubert, DH
Whiteley, JM
Wang, L
Hoch, JA
机构
[1] Scripps Res Inst, Dept Mol & Expt Med, La Jolla, CA 92037 USA
[2] RW Johnson Pharmaceut Res Inst, Raritan, NJ 08869 USA
关键词
D O I
10.1073/pnas.95.9.5317
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
A class of antibacterials has been discovered that inhibits the growth of Gram-positive pathogenic bacteria. RWJ-49815, a representative of a family of hydrophobic tyramines, in addition to being a potent bactericidal Grampositive antibacterial, inhibits the autophosphorylation of kinase A of the KinA::Spo0F two-component signal transduction system in vitro. Analogs of RWJ-49815 vary greatly in their ability to inhibit growth of bacteria and this ability correlates directly with their activity as kinase A inhibitors. Compared with the potent quinolone, ciprofloxacin, RWJ-49815 exhibits reduced resistance emergence in a laboratory passage experiment. Inhibition of the histidine protein kinase::response regulator two component signal transduction pathways may present an opportunity to depress chromosomal resistance emergence by targeting multiple proteins with a single inhibitor in a single bacterium. Such inhibitors may represent a class of antibacterials that potentially may represent a breakthrough in antibacterial therapy.
引用
收藏
页码:5317 / 5322
页数:6
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