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Base-pair dynamics in an antiparallel DNA triplex measured by catalyzed imino proton exchange monitored via 1H NMR spectroscopy.

机译:通过1H NMR光谱监测的催化亚氨基质子交换测量的反平行DNA三链体中的碱基对动力学。

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Using (1)H NMR spectroscopy, the base-pair opening dynamics of an antiparallel foldback DNA triplex and the corresponding duplex has been characterized via catalyzed imino proton exchange. The triplex system was found to be in an equilibrium between a duplex and a triplex form. The exchange rate between the two forms (i.e., the on/off-rate of the third strand) was measured to be 5 s(-1) at 1 degrees C, and the base-pair dynamics of both forms were investigated separately. Both Watson-Crick and reverse Hoogsteen base pairs were found to have base-pair lifetimes in the order of milliseconds. The stability of the Watson-Crick base pairs was, however, substantially increased in the presence of the third strand. In the DNA triplex, the opening dynamics of the reverse Hoogsteen base pairs was significantly faster than the dynamics of the Watson-Crick pairs. We were able to conclude that, for both Watson-Crick and reverse Hoogsteen base pairs, spontaneous and individual opening from within the closed base triplet is the dominating opening pathway.
机译:使用(1)NMR光谱学,已通过催化亚氨基质子交换表征了反平行折叠DNA三链体和相应双链体的碱基对开放动力学。发现三链体系统在双链体和三链体形式之间处于平衡。两种形式之间的交换速率(即第三链的开/关速率)在1摄氏度下测量为5 s(-1),并且分别研究了两种形式的碱基对动力学。发现Watson-Crick和反向Hoogsteen碱基对的碱基对寿命均以毫秒为单位。但是,在第三条链的存在下,沃森-克里克碱基对的稳定性大大提高了。在DNA三链体中,反向Hoogsteen碱基对的开放动力学显着快于Watson-Crick对的动力学。我们能够得出结论,对于Watson-Crick和反向Hoogsteen碱基对,从封闭的碱基三联体内部自发和个体打开是主要的开放途径。

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