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Free energy landscape and transition pathways from Watson-Crick to Hoogsteen base pairing in free duplex DNA

机译:自由双链DNA中从Watson-Crick到Hoogsteen碱基配对的自由能景观和过渡途径

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Houghton (HG) base pairing plays a central role in the DNA binding of proteins and small ligands. Probing detailed transition mechanism from Watson-Crick (WC) to HG base pair (bp) formation in duplex DNAs is of fundamental importance in terms of revealing intrinsic functions of double helical DNAs beyond their sequence determined functions. We investigated a free energy landscape of a free B-DNA with an adenosine-thymine (A-T) rich sequence to probe its conformational transition pathways from WC to HG base pairing. The free energy landscape was computed with a state-of-art two-dimensional umbrella molecular dynamics simulation at the all-atom level. The present simulation showed that in an isolated duplex DNA, the spontaneous transition from WC to HG bp takes place via multiple pathways. Notably, base flipping into the major and minor grooves was found to play an important role in forming these multiple transition pathways. This finding suggests that naked B-DNA under normal conditions has an inherent ability to form HG bps via spontaneous base opening events.
机译:霍顿(HG)碱基配对在蛋白质和小配体的DNA结合中起着核心作用。就揭示双螺旋DNA的固有功能超出其序列决定的功能而言,探索双链DNA中从Watson-Crick(WC)到HG碱基对(bp)形成的详细过渡机制至关重要。我们研究了富含腺苷-胸腺嘧啶(A-T)序列的自由B-DNA的自由能景观,以探究其从WC到HG碱基配对的构象转变途径。自由能态是通过在所有原子水平上进行的最新二维伞状分子动力学模拟计算得出的。目前的模拟表明,在分离的双链DNA中,从WC到HG bp的自发转变是通过多种途径发生的。值得注意的是,发现基部翻转进入主要和次要凹槽在形成这些多重过渡途径中起着重要作用。该发现表明,裸露的B-DNA在正常条件下具有通过自发碱基打开事件形成HG bps的固有能力。

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