Abstract

Two-component signal transduction systems allow bacteria to sense and respond rapidly to changes in their environment leading to specific gene activation or repression. These two-component systems are integral in the ability of pathogenic bacteria to mount and establish a successful infection within the host and, consequently, have been recognized as targets for new anti-microbial agents. In this paper, we define the site and mechanism of action of several previously identified inhibitors of bacterial two-component systems. We show that the most potent inhibitors target the carboxyl-terminal catalytic domain of the sensor kinase and exert their affect by causing structural alterations of the kinase leading to aggregation. Recognition of this phenomenon has important implications for the development of novel inhibitors of two-component systems and should facilitate the rapid identification and elimination of compounds with nonspecific affects from medicinal chemistry drug discovery programs.

Highlights

  • Bacteria are highly adaptive organisms capable of growth in an extreme variety of carbon and nitrogen sources and environmental conditions

  • These two-component systems are integral in the ability of pathogenic bacteria to mount and establish a successful infection within the host and, have been recognized as targets for new antimicrobial agents

  • Two-component signal transduction systems play a key role in controlling virulence responses of a wide variety of bacterial pathogens [3]

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Summary

Introduction

Bacteria are highly adaptive organisms capable of growth in an extreme variety of carbon and nitrogen sources and environmental conditions. When compared with control reactions addition of the inhibitor compounds resulted in varying levels of inhibition of autokinase and phosphotransfer activities of the purified components

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