首页> 外文期刊>Biochemistry >The GAAA Tetraloop-Receptor Interaction Contributes Differentially to Folding Thermodynamics and Kinetics for the P4-P6 RNA Domain.
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The GAAA Tetraloop-Receptor Interaction Contributes Differentially to Folding Thermodynamics and Kinetics for the P4-P6 RNA Domain.

机译:GaAA Tetraloop-受体相互作用效果差异地折叠P4-P6 RNA结构域的热力学和动力学。

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Tetraloops with the generic sequence GNRA are commonly found in RNA secondary structure, and interactions of such tetraloops with "receptors" elsewhere in RNA play important roles in RNA structure and folding. However, the contributions of tetraloop-receptor interactions specifically to the kinetics of RNA tertiary folding, rather than the thermodynamics of maintaining tertiary structure once folded, have not been reported. Here we investigate the role of the key GAAA tetraloop-receptor motif in folding of the P4-P6 domain of the Tetrahymena group I intron RNA. Insertions of one or more nucleotides into the tetraloop significantly disrupt the thermodynamics of tertiary folding; single-nucleotide insertions shift the folding free energy by 2-4 kcal/mol (DeltaDeltaG degrees '). The folding kinetics of several modified P4-P6 domains were determined by stopped-flow fluorescence spectroscopy, using an internally incorporated pyrene residue as the chromophore. In contrast to the thermodynamic results, the kinetics of Mg(2+)-induced folding were barely affected by the tetraloop modifications, with a DeltaDeltaG() of 0.2-0.4 kcal/mol and a Phi value (ratio of the kinetic and thermodynamic contributions) of <0.1. These data indicate an early transition state for folding of P4-P6 with respect to forming the tetraloop-receptor contact, consistent with previous results for modifications elsewhere in P4-P6. We conclude that the GAAA tetraloop-receptor motif contributes little to the stabilization of the transition state for Mg(2+)-induced P4-P6 folding. Rather, the tetraloop-receptor motif acts to clamp the RNA once folding has occurred. This is the first report to correlate the kinetic and thermodynamic contributions of an important RNA tertiary motif, the GNRA tetraloop-receptor. The results are related to possible models for the Mg(2+)-induced folding of the P4-P6 RNA, including a model invoking rapid nonspecific electrostatic collapse.
机译:带有通用序列GNRA的向量ralops通常在RNA二级结构中发现,并且在RNA中其他地方的其他Tetraloops与“受体”的相互作用在RNA结构和折叠中起重要作用。然而,尚未报道Tetraloop-受体相互作用特异性对RNA三级折叠的动力学的贡献,而不是维持三级结构一旦折叠的热力学。在这里,我们研究了关键GaAA Tetralop-actory基序的作用在Tetrahymena组I内含子RNA的P4-P6结构域的折叠中。将一种或多种核苷酸插入到图罗级的核苷酸显着破坏了三级折叠的热力学;单核苷酸插入将折叠自由能量换成2-4千卡/摩尔(DeltaDeltag Degete')。通过止流荧光光谱法测定几种改性P4-P6结构域的折叠动力学,使用内部掺入的芘残基作为发色团。与热力学结果相比,Mg(2 +)诱导的折叠的动力学几乎受到Tetralop修饰的影响,具有0.2-0.4kcal / mol的DeltaDeltag()和Phi值(动力学和热力学贡献的比率) )<0.1。这些数据表明了用于折叠P4-P6的早期过渡状态,相对于形成Tetraloop-受体接触,与先前的P4-P6中其他地方的改进结果一致。我们得出结论,GaAA Tetraloop-受体基序对Mg(2 +)诱导的P4-P6折叠的过渡状态有助于稳定。相反,一旦发生折叠,Tetraloop-受体基序就可以夹紧RNA。这是第一个将重要RNA第三族主题,GNRA Tetraloop-受体相关联的动力动力学贡献的报告。结果与Mg(2 +)的可能模型有关 - 诱导P4-P6 RNA的折叠,包括调用快速非特异性静电塌陷的模型。

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