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Estimation of Binding Constants of Peptide Nucleic Acid and Secondary-Structured DNA by Affinity Capillary Electrophoresis

机译:亲和毛细管电泳估计肽核酸和二级结构DNA的结合常数

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An affinity capillary electrophoresis method was developed to determine a binding constant between a peptide nucleic acid (PNA) and a hairpin-structured DNA. A diblock copolymer composed of PNA and polyethylene glycol (PEG) was synthesized as a novel affinity probe. The base sequence of the probe's PNA segment was complementary to a hairpin-structured region of a 60-base single-stranded DNA (ssDNA). Upon applying a voltage, the DNA hairpin migrated slowly compared to a random sequence ssDNA in the presence of the PNA probe. This retardation was induced by strand invasion of the PNA into the DNA hairpin to form a hybridized complex, where the PEG segment received a large amount of hydrodynamic friction during electrophoresis. The binding constant between the PNA probe and the DNA hairpin was easily determined by mobility analysis. This simple method would be potentially beneficial in studying binding behaviors of various artificial nucleotides to natural DNA or RNA.
机译:开发了一种亲和毛细管电泳方法来确定肽核酸(PNA)和发夹结构的DNA之间的结合常数。合成了由PNA和聚乙二醇(PEG)组成的二嵌段共聚物作为新型亲和探针。探针的PNA片段的碱基序列与60碱基单链DNA(ssDNA)的发夹结构区域互补。施加电压后,与存在PNA探针的随机序列ssDNA相比,DNA发夹迁移缓慢。这种阻滞是通过PNA链侵入DNA发夹中形成杂交复合物而引起的,其中PEG片段在电泳过程中受到大量流体动力摩擦。通过迁移率分析容易地确定PNA探针和DNA发夹之间的结合常数。这种简单的方法在研究各种人工核苷酸与天然DNA或RNA的结合行为方面可能会有益。

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