4.6 Article

Allosteric regulation of the nickel-responsive NikR transcription factor from Helicobacter pylori

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JOURNAL OF BIOLOGICAL CHEMISTRY
卷 296, 期 -, 页码 -

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DOI: 10.1074/jbc.RA120.015459

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  1. Canadian Institutes of Health Research [MOP-123483]
  2. Natural Sciences and Engineering Research Council of Canada [418679]

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Nickel plays a crucial role in the survival of the pathogenic bacteria Helicobacter pylori in the human stomach by regulating nickel homeostasis through the transcription factor NikR. Nickel binding induces conformational changes in HpNikR, enabling it to bind specific DNA motifs and influence gene transcription. Zinc is unable to induce the same allosteric response as nickel, suggesting that the mechanism of nickel-activated DNA binding by HpNikR is driven by conformational selection.
Nickel is essential for the survival of the pathogenic bacteria Helicobacter pylori in the fluctuating pH of the human stomach. Due to its inherent toxicity and limited availability, nickel homeostasis is maintained through a network of pathways that are coordinated by the nickel-responsive transcription factor NikR. Nickel binding to H. pylori NikR (HpNikR) induces an allosteric response favoring a conformation that can bind specific DNA motifs, thereby serving to either activate or repress transcription of specific genes involved in nickel homeostasis and acid adaptation. Here, we examine how nickel induces this response using 19F-NMR, which reveals conformational and dynamic changes associated with nickel-activated DNA complex formation. HpNikR adopts an equilibrium between an open state and DNA-binding competent states regardless of nickel binding, but a higher level of dynamics is observed in the absence of metal. Nickel binding shifts the equilibrium toward the binding-competent states and decreases the mobility of the DNA-binding domains. The nickelbound protein is then able to adopt a single conformation upon binding a target DNA promoter. Zinc, which does not promote high-affinity DNA binding, is unable to induce the same allosteric response as nickel. We propose that the allosteric mechanism of nickel-activated DNA binding by HpNikR is driven by conformational selection.

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