Ma Cong, Yang Xiao, Lewis Peter J
School of Environmental and Life Sciences, University of Newcastle, Callaghan, NSW, Australia.
School of Environmental and Life Sciences, University of Newcastle, Callaghan, NSW, Australia
Microbiol Mol Biol Rev. 2016 Jan 13;80(1):139-60. doi: 10.1128/MMBR.00055-15. Print 2016 Mar.
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.
转录是基因表达的第一步,由RNA聚合酶(RNAP)催化完成,并通过与一系列蛋白质转录因子相互作用进行调控。RNAP及其相关转录因子在细菌领域高度保守,是发现广谱抗菌剂的理想靶点。尽管市场上有众多抗生素,但目前仅批准了两个靶向转录的系列药物。过去15年中高分辨率解析的RNAP和转录复合物三维结构,重新激发了人们利用基于结构的合理方法,针对这一关键过程开发抗生素的兴趣。在本综述中,我们结合RNAP的结构研究描述了对细菌转录过程的抑制作用,强调了新型转录抑制剂发现方面的最新进展,并提出了合理药物设计的其他潜在抗菌靶点。