细菌转录抑制因子NrdR -一种灵活的多因子核苷酸传感器。

Inna Rozman Grinberg, Ornella Bimaï, Saher Shahid, Lena Philipp, Markel Martínez-Carranza, Ipsita Banerjee, Daniel Lundin, Pål Stenmark, Britt-Marie Sjöberg, Derek T Logan
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摘要

NrdR是一种细菌转录抑制因子,由锌带结构域和atp锥结构域组成。了解其作用机制有助于设计新型抗菌药物。NrdR特异性结合核糖核苷酸还原酶操作子上游的两个“NrdR盒子”,其中大肠杆菌有三个:nrdHIEF, nrdDG和nrdAB,我们在最后一个盒子中发现了一个新的盒子。我们发现,当负载ATP +脱氧腺苷三磷酸(dATP)或等效的二磷酸组合时,大肠杆菌NrdR (EcoNrdR)对这三个位点具有相似的结合强度。没有其他的腺嘌呤核苷酸组合能促进与DNA的结合。我们提出了EcoNrdR-ATP-dATP和EcoNrdR-ADP-dATP的晶体结构,这是NrdR的第一个高分辨率晶体结构。我们还确定了dna结合的EcoNrdR-ATP- datp的低温电镜结构和EcoNrdR-ATP的新细丝。四聚体形式的EcoNrdR涉及锌带结构域和atp锥对之间的交替相互作用。该结构在atp锥与锌带结构域的相对取向上显示出相当大的灵活性。DNA结合的EcoNrdR-ATP-dATP的结构表明,DNA结合时atp锥与锌带之间的构象重排明显,而atp锥保持相同的相对取向。相反,装载atp的EcoNrdR细丝显示atp -锥对的重排,并隔离NrdR的DNA结合残基,使它们无法与DNA结合。我们的研究结果,结合之前的结构和生化研究,指向高度灵活的EcoNrdR结构,当装载正确的核苷酸时,适应最佳的启动子结合构象。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Bacterial transcriptional repressor NrdR - a flexible multifactorial nucleotide sensor.

NrdR is a bacterial transcriptional repressor consisting of a zinc (Zn)-ribbon domain followed by an ATP-cone domain. Understanding its mechanism of action could aid the design of novel antibacterials. NrdR binds specifically to two "NrdR boxes" upstream of ribonucleotide reductase operons, of which Escherichia coli has three: nrdHIEF, nrdDG and nrdAB, in the last of which we identified a new box. We show that E. coli NrdR (EcoNrdR) has similar binding strength to all three sites when loaded with ATP plus deoxyadenosine triphosphate (dATP) or equivalent diphosphate combinations. No other combination of adenine nucleotides promotes binding to DNA. We present crystal structures of EcoNrdR-ATP-dATP and EcoNrdR-ADP-dATP, which are the first high-resolution crystal structures of an NrdR. We have also determined cryo-electron microscopy structures of DNA-bound EcoNrdR-ATP-dATP and novel filaments of EcoNrdR-ATP. Tetrameric forms of EcoNrdR involve alternating interactions between pairs of Zn-ribbon domains and ATP-cones. The structures reveal considerable flexibility in relative orientation of ATP-cones vs Zn-ribbon domains. The structure of DNA-bound EcoNrdR-ATP-dATP shows that significant conformational rearrangements between ATP-cones and Zn-ribbons accompany DNA binding while the ATP-cones retain the same relative orientation. In contrast, ATP-loaded EcoNrdR filaments show rearrangements of the ATP-cone pairs and sequester the DNA-binding residues of NrdR such that they are unable to bind to DNA. Our results, in combination with a previous structural and biochemical study, point to highly flexible EcoNrdR structures that, when loaded with the correct nucleotides, adapt to an optimal promoter-binding conformation.

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