MacDougall Iain J A, Lewis Peter J, Griffith Renate
School of Environmental and Life Sciences, The University of Newcastle, Biology Building, Callaghan, NSW 2308, Australia.
J Mol Graph Model. 2005 Jan;23(4):297-303. doi: 10.1016/j.jmgm.2004.10.001.
RNA polymerase (RNAP) is the central enzyme of transcription and requires interaction with transcription factors in vivo for correct processivity. Both the transcription initiation complex and the ternary elongation complex are stabilised by and require protein-protein interactions between the various components involved. These interactions may form the basis for rational design of small peptide mimics of one or more proteins involved in order to inhibit protein-protein interactions and thus transcription. Here, we present homology models of the model Gram positive organism Bacillus subtilis RNA polymerase in the core and holoenzyme forms. Interactions between RNA polymerase and the transcription factor sigmaA were investigated in order to design peptide mimics of the major interactions.
RNA聚合酶(RNAP)是转录的核心酶,在体内需要与转录因子相互作用以实现正确的持续合成能力。转录起始复合物和三元延伸复合物都通过参与的各种组分之间的蛋白质-蛋白质相互作用而稳定,并且需要这些相互作用。这些相互作用可能为合理设计参与其中的一种或多种蛋白质的小肽模拟物提供基础,以便抑制蛋白质-蛋白质相互作用从而抑制转录。在此,我们展示了模式革兰氏阳性菌枯草芽孢杆菌RNA聚合酶核心形式和全酶形式的同源模型。为了设计主要相互作用的肽模拟物,研究了RNA聚合酶与转录因子sigmaA之间的相互作用。