Bacterial Transcription as a Target for Antibacterial Drug Development

被引:101
作者
Ma, Cong [1 ]
Yang, Xiao [1 ]
Lewis, Peter J. [1 ]
机构
[1] Univ Newcastle, Sch Environm & Life Sci, Callaghan, NSW 2308, Australia
基金
澳大利亚研究理事会; 英国医学研究理事会;
关键词
COLI RNA-POLYMERASE; TERMINATION FACTOR-RHO; RAY CRYSTAL-STRUCTURES; PEPTIDE MICROCIN J25; ESCHERICHIA-COLI; STRUCTURAL BASIS; BINDING-SITE; BIOLOGICAL-ACTIVITY; SWITCH REGION; BETA-SUBUNIT;
D O I
10.1128/MMBR.00055-15
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Transcription, the first step of gene expression, is carried out by the enzyme RNA polymerase (RNAP) and is regulated through interaction with a series of protein transcription factors. RNAP and its associated transcription factors are highly conserved across the bacterial domain and represent excellent targets for broad-spectrum antibacterial agent discovery. Despite the numerous antibiotics on the market, there are only two series currently approved that target transcription. The determination of the three-dimensional structures of RNAP and transcription complexes at high resolution over the last 15 years has led to renewed interest in targeting this essential process for antibiotic development by utilizing rational structure-based approaches. In this review, we describe the inhibition of the bacterial transcription process with respect to structural studies of RNAP, highlight recent progress toward the discovery of novel transcription inhibitors, and suggest additional potential antibacterial targets for rational drug design.
引用
收藏
页码:139 / 160
页数:22
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