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

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

作者信息

Wärmländer Sebastian, Sandström Karin, Leijon Mikael, Gräslund Astrid

机构信息

Department of Biochemistry and Biophysics, Arrhenius Laboratory, Stockholm University, S-106 91 Stockholm, Sweden.

出版信息

Biochemistry. 2003 Nov 4;42(43):12589-95. doi: 10.1021/bi034479u.

Abstract

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.

摘要

利用核磁共振氢谱(¹H NMR),通过催化亚氨基质子交换对反平行回折DNA三链体及其相应双链体的碱基对打开动力学进行了表征。发现三链体系统处于双链体和三链体形式之间的平衡状态。两种形式之间的交换速率(即第三条链的结合/解离速率)在1℃下测得为5 s⁻¹,并且分别研究了两种形式的碱基对动力学。发现沃森-克里克碱基对和反向 hoogsteen 碱基对的碱基对寿命均在毫秒级。然而,在第三条链存在的情况下,沃森-克里克碱基对的稳定性显著增加。在DNA三链体中,反向 hoogsteen 碱基对的打开动力学明显快于沃森-克里克碱基对的动力学。我们能够得出结论,对于沃森-克里克碱基对和反向 hoogsteen 碱基对,从封闭碱基三联体内自发且单个打开是主要的打开途径。

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