Comparative analyses of N-acylated homoserine Lactones reveal unique structural features that dictate their ability to activate or inhibit quorum sensing

被引:102
作者
Geske, Grant D. [1 ]
ONeill, Jennifer C. [1 ]
Miller, David M.
Wezeman, Rachel J.
Mattmann, Margrith E. [1 ]
Lin, Qi [1 ]
Blackwell, Helen E. [1 ]
机构
[1] Univ Wisconsin, Dept Chem, Madison, WI 53706 USA
关键词
combinatorial chemistry; gram-negative bacteria; homoserine lactones; quorum sensing; structure-activity relationships;
D O I
10.1002/cbic.200700551
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
Bacterial quorum sensing, is mediated by low molecular-weight signals and ploys a critical role in both the pathogenesis of infectious disease and beneficial symbioses. There is significant interest in the development of synthetic ligands that can intercept bacterial quorum sensing signals and modulate these outcomes. Here, we report the design and comparative analysis of the effects of similar to 90 synthetic N-acylated homoserine lactones (AHLs) on quorum sensing in three Gram negative bacterial species and a critical examination of the structural features of these ligands that dictate agonistic and antagonistic activity, and selectivity for different R protein targets. These studies have revealed the most comprehensive set of structure-activity relationships to date that direct AHL-mediated quorum sensing and a new set of chemical probes with which to study this complex signaling process. Furthermore, this work provides a foundation on which to design next-generation quorum sensing modulators with improved activities and selectivities.
引用
收藏
页码:389 / 400
页数:12
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