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α-Hemolysin nanopore studies reveal strong interactions between biogenic polyamines and DNA hairpins

机译:α-溶血素纳米孔研究揭示了生物多胺与DNA发夹之间的强相互作用

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摘要

The α-hemolysin (α-HL) nanopore analyzes DNA as it is electrophoretically driven through the pore. The respective current vs. time (i-t) traces depends on the DNA sequence, its secondary structures, or on the physical conditions of the analysis. The current study describes analysis of a DNA hairpin with a 5'-extension with the α-HL nanopore in the presence of the polyamines spermine (Spm), spermidine (Spd), and putrescine (Put). These studies identified a new i-t trace characteristic of the DNA-polyamine complex. Voltage-dependent studies determined that the hairpin-Spm complex formed with excess Spm was not unzipped and translocated through the pore even when the voltage was increased to 180 mV. The DNA hairpin sample was titrated with Spm, Spd, or Put that showed a dose-dependent response in the characteristic event patterns for hairpins bound to Spm or Spd, but not for Put. Plots of the event types vs. count were used to calculate binding constants for the Spm or Spd hairpin interactions under these conditions. The titration also demonstrated that the event rate decreased ~10-fold when the Spm or Spd concentration was increased from 0 to 4 mM. These observations impose practical limitations on the ability to use Spm or Spd for DNA studies with the α-HL nanopore.
机译:α-溶血素(α-HL)纳米孔可分析通过电泳驱动的DNA。各自的电流与时间(i-t)轨迹取决于DNA序列,其二级结构或分析的物理条件。当前的研究描述了在存在多胺精胺(Spm),亚精胺(Spd)和腐胺(Put)的情况下使用α-HL纳米孔对5'延伸的DNA发夹的分析。这些研究确定了DNA-多胺复合物的新的i-t痕迹特征。电压依赖性研究确定,即使电压增加到180 mV,由过量Spm形成的发夹结构-Spm复合物也不会解开并通过孔转移。 DNA发夹样品用Spm,Spd或Put进行滴定,该特征在与Spm或Spd结合的发夹的特征事件模式中显示出剂量依赖性响应,但Put则不。事件类型与计数的关系图用于计算在这些条件下Spm或Spd发夹相互作用的结合常数。滴定还表明,当Spm或Spd浓度从0增加到4 mM时,事件发生率降低〜10倍。这些观察结果限制了使用Spm或Spd进行α-HL纳米孔DNA研究的能力。

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