Two-component signal transduction as potential drug targets in pathogenic bacteria

被引:258
|
作者
Gotoh, Yasuhiro [1 ]
Eguchi, Yoko [1 ]
Watanabe, Takafumi [1 ]
Okamoto, Sho [1 ]
Doi, Akihiro [1 ]
Utsumi, Ryutaro [1 ]
机构
[1] Kinki Univ, Grad Sch Agr, Dept Biosci, Nara 6318505, Japan
基金
日本学术振兴会;
关键词
BIOSYNTHESIS-ACTIVATING PHEROMONE; III PROTEIN SECRETION; STAPHYLOCOCCUS-AUREUS; ERWINIA-AMYLOVORA; MOLECULAR CHARACTERIZATION; TRANSCRIPTIONAL ACTIVATOR; GENE-TRANSCRIPTION; REGULATORY SYSTEM; BIOFILM FORMATION; HISTIDINE KINASE;
D O I
10.1016/j.mib.2010.01.008
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Gene clusters contributing to processes such as cell growth and pathogenicity are often controlled by two-component signal transduction systems (TCSs). Specific inhibitors against TCS systems work differently from conventional antibiotics, and developing them into new drugs that are effective against various drug-resistant bacteria may be possible. Furthermore, inhibitors of TCSs that control virulence factors may reduce virulence without killing the pathogenic bacteria. Previous TCS inhibitors targeting the kinase domain of the histidine kinase sensor suffered from poor selectivity. Recent TCS inhibitors, however, target the sensory domains of the sensors blocking the quorum sensing system, or target the essential response regulator. These new targets are introduced, together with several specific TCSs that have the potential to serve as effective drug targets.
引用
收藏
页码:232 / 239
页数:8
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