Developing inhibitors to selectively target two-component and phosphorelay signal transduction systems of pathogenic microorganisms

被引:75
作者
Stephenson, K
Hoch, JA
机构
[1] Scripps Res Inst, Dept Mol & Expt Med, Div Cellular Biol, La Jolla, CA 92037 USA
[2] Univ Leeds, Sch Biochem & Mol Biol, Div Microbiol, Leeds, W Yorkshire, England
关键词
two-component system; phosphorelay; sensor histidine kinase; response regulator; virulence; inhibitor;
D O I
10.2174/0929867043455765
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
Two-component signal transduction systems and their expanded variants known as phosphorelays are integral elements of the virulence and antimicrobial resistance responses of a wide range of pathogenic bacteria and fungi and also regulate essential functions. As a consequence, two-component systems and phosphorelays are recognized targets for the development of novel antimicrobial agents and a number of chemically synthesized inhibitors from different chemical classes have been identified by compound library screens. However, in the majority of cases these compounds do not appear to be selective for signal transduction pathways and exert their effect by multiple mechanisms of action. The key to designing molecules to selectively disrupt signal transduction may lie with the conserved features of response regulators and the structural analysis of complexes of signaling proteins.
引用
收藏
页码:765 / 773
页数:9
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