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DNA mimicry by a high-affinity anti-NF-κB RNA aptamer

机译:高亲和力的抗NF-κBRNA适体的DNA模仿

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摘要

The binding of RNA molecules to proteins or other ligands can require extensive RNA folding to create an induced fit. Understanding the generality of this principle involves comparing structures of RNA before and after complex formation. Here we report the NMR solution structure of a 29-nt RNA aptamer whose crystal structure had previously been determined in complex with its transcription factor target, the p502 form of NF-κB. The RNA aptamer internal loop structure has pre-organized features that are also found in the complex, including non-canonical base pairing and cross-strand base stacking. Remarkably, the free RNA aptamer structure possesses a major groove that more closely resembles B-form DNA than RNA. Upon protein binding, changes in RNA structure include the kinking of the internal loop and distortion of the terminal tetraloop. Thus, complex formation involves both pre-formed and induced fit binding interactions. The high affinity of the NF-κB transcription factor for this RNA aptamer may largely be due to the structural pre-organization of the RNA that results in its ability to mimic DNA.
机译:RNA分子与蛋白质或其他配体的结合可能需要大量的RNA折叠才能产生诱导的拟合。了解该原理的一般性涉及比较复合物形成前后的RNA结构。在这里,我们报告了一种29 nt RNA适体的NMR溶液结构,该晶体的晶体结构先前已与其转录因子靶标(NF-κB的p502形式)复杂地确定。 RNA适体内部环结构具有在复合物中也发现的预组织特征,包括非规范碱基配对和跨链碱基堆积。值得注意的是,游离RNA适体结构具有一个主要沟,该沟比RNA更类似于B型DNA。蛋白质结合后,RNA结构的变化包括内部环的扭结和末端四环的扭曲。因此,复合物的形成涉及预形成的和诱导的拟合结合相互作用。 NF-κB转录因子对此RNA适体的高亲和力可能主要是由于RNA的结构预组织,从而导致其模仿DNA的能力。

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