Deducing receptor signaling parameters from in vivo analysis:: LuxN/AI-1 quorum sensing in Vibrio harveyi

被引:79
作者
Swem, Lee R. [1 ]
Swem, Danielle L. [1 ,2 ]
Wingreen, Ned S. [1 ]
Bassler, Bonnie L. [1 ,2 ]
机构
[1] Princeton Univ, Dept Mol Biol, Princeton, NJ 08544 USA
[2] Howard Hughes Med Inst, Chevy Chase, MD 20815 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
D O I
10.1016/j.cell.2008.06.023
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
Quorum sensing, a process of bacterial cell-cell communication, relies on production, detection, and response to autoinducer signaling molecules. LuxN, a nine-transmembrane domain protein from Vibrio harveyi, is the founding example of membrane-bound receptors for acyl-homoserine lactone (AHL) autoinducers. We used mutagenesis and suppressor analyses to identify the AHL-binding domain of LuxN and discovered LuxN mutants that confer both decreased and increased AHL sensitivity. Our analysis of dose-response curves of multiple LuxN mutants pins these inverse phenotypes on quantifiable opposing shifts in the free-energy bias of LuxN for occupying its kinase and phosphatase states. To understand receptor activation and to characterize the pathway signaling parameters, we exploited a strong LuxN antagonist, one of fifteen small-molecule antagonists we identified. We find that quorum-sensing-mediated communication can be manipulated positively and negatively to control bacterial behavior and, more broadly, that signaling parameters can be deduced from in vivo data.
引用
收藏
页码:461 / 473
页数:13
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