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Triple helical DNA in a duplex context and base pair opening

机译:在双链体和碱基对开放的情况下三螺旋DNA

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It is fundamental to explore in atomic detail the behavior of DNA triple helices as a means to understand the role they might play in vivo and to better engineer their use in genetic technologies, such as anti-gene therapy. To this aim we have performed atomistic simulations of a purine-rich antiparallel triple helix stretch of 10 base triplets flanked by canonical Watson-Crick double helices. At the same time we have explored the thermodynamic behavior of a flipping Watson-Crick base pair in the context of the triple and double helix. The third strand can be accommodated in a B-like duplex conformation. Upon binding, the double helix changes shape, and becomes more rigid. The triple-helical region increases its major groove width mainly by oversliding in the negative direction. The resulting conformations are somewhere between the A and B conformations with base pairs remaining almost perpendicular to the helical axis. The neighboring duplex regions maintain a B DNA conformation. Base pair opening in the duplex regions is more probable than in the triplex and binding of the Hoogsteen strand does not influence base pair breathing in the neighboring duplex region.
机译:基本了解原子三重螺旋的行为是了解它们在体内可能发挥的作用并更好地设计其在遗传技术(例如抗基因疗法)中的用途的一种手段。为此,我们进行了富嘌呤反平行三螺旋拉伸的原子模拟,该三螺旋拉伸由10个基本三联体构成,两侧是规范的Watson-Crick双螺旋。同时,我们在三重和双重螺旋的背景下研究了翻转的Watson-Crick碱基对的热力学行为。第三链可以以B样双链体构象容纳。结合后,双螺旋线改变形状,并变得更坚硬。三螺旋区主要通过在负方向上过度滑动来增加其主要凹槽宽度。所得构象在A和B构象之间的某处,碱基对几乎保持垂直于螺旋轴。相邻的双链体区域保持B DNA构象。双链体区域中的碱基对开放比三链体中的开放更可能,并且Hoogsteen链的结合不会影响相邻双链体区域中的碱基对呼吸。

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