通过监测自互补序列的发夹-双工平衡来研究阳离子与核苷酸的结合。

Shu-ichi Nakano, Hidenobu Hirayama, Naoki Sugimoto
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引用次数: 1

摘要

核苷酸折叠伴随着阳离子结合,屏蔽了磷酸基团的电负性电位,缩合层中的金属离子主要与碱基配对的核苷酸扩散结合。虽然在特定位点结合的金属离子已经得到了很好的研究,但扩散结合的阳离子的信息还没有得到充分的研究,这些阳离子的结合亲和力通常比在特定位点结合的阳离子弱。我们探索了一种方便的实验系统,使用自互补的核苷酸序列来分析扩散结合到DNA或RNA碱基对的阳离子配体。为了研究非同源水条件下金属离子与核苷酸的相互作用,研究了含有大量聚乙二醇的溶液。我们发现聚乙二醇(例如,20% wt%)显著影响了金属离子与核苷酸的结合,这表明分子环境对核苷酸-阳离子相互作用的重要性。
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Investigations of the cation binding to nucleotides by monitoring the hairpin-duplex equilibrium of a self-complementary sequence.

Nucleotide folding accompanies cation binding that shields the electronegative potential of phosphate groups, and metal ions in the condensation layer predominantly associate diffusely with base-paired nucleotides. Although metal ions bound at specific sites have been well studied, information of diffusely bound cations, that usually have a weak binding affinity than those associating at specific sites, have not been thoroughly studied. We explored a convenient experimental system using a self-complementary nucleotide sequence for analyzing cationic ligands diffusely bound to DNA or RNA base pairs. To study the metal ion-nucleotide interaction under a non-homologous aqueous condition, solutions containing a large amount of PEG (polyethylene glycol) were examined. We found that PEG (e.g., 20 wt%) substantially influenced the metal ion binding to nucleotides, suggesting significances of the molecular environment on nucleotide-cation interactions.

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