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首页> 外文期刊>Journal of Molecular Biology >1 A crystal structures of B-DNA reveal sequence-specific binding and groove-specific bending of DNA by magnesium and calcium.
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1 A crystal structures of B-DNA reveal sequence-specific binding and groove-specific bending of DNA by magnesium and calcium.

机译:1 B-DNA的晶体结构揭示了镁和钙对DNA的序列特异性结合和凹槽特异性弯曲。

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The 1 A resolution X-ray crystal structures of Mg(2+) and Ca(2+) salts of the B-DNA decamers CCAACGTTGG and CCAGCGCTGG reveal sequence-specific binding of Mg(2+) and Ca(2+) to the major and minor grooves of DNA, as well as non-specific binding to backbone phosphate oxygen atoms. Minor groove binding involves H-bond interactions between cross-strand DNA base atoms of adjacent base-pairs and the cations' water ligands. In the major groove the cations' water ligands can interact through H-bonds with O and N atoms from either one base or adjacent bases, and in addition the softer Ca(2+) can form polar covalent bonds bridging adjacent N7 and O6 atoms at GG bases. For reasons outlined earlier, localized monovalent cations are neither expected nor found.Ultra-high atomic resolution gives an unprecedented view of hydration in both grooves of DNA, permits an analysis of individual anisotropic displacement parameters, and reveals up to 22 divalent cations per DNA duplex. Each DNA helix is quite anisotropic, and alternate conformations, with motion in the direction of opening and closing the minor groove, are observed for the sugar-phosphate backbone. Taking into consideration the variability of experimental parameters and crystal packing environments among these four helices, and 24 other Mg(2+) and Ca(2+) bound B-DNA structures, we conclude that sequence-specific and strand-specific binding of Mg(2+) and Ca(2+) to the major groove causes DNA bending by base-roll compression towards the major groove, while sequence-specific binding of Mg(2+) and Ca(2+) in the minor groove has a negligible effect on helix curvature. The minor groove opens and closes to accommodate Mg(2+) and Ca(2+) without the necessity for significant bending of the overall helix.The program Shelxdna was written to facilitate refinement and analysis of X-ray crystal structures by Shelxl-97 and to plot and analyze one or more Curves and Freehelix output files. Copyright 2000 Academic Press.
机译:B-DNA骗子CCAACGTTGG和CCAGCGCTGG的Mg(2+)和Ca(2+)盐的1 A分辨率X射线晶体结构揭示了Mg(2+)和Ca(2+)的序列特异性结合DNA的主要和次要凹槽,以及与骨架磷酸氧原子的非特异性结合。小沟结合涉及相邻碱基对的跨链DNA碱基原子与阳离子的水配体之间的H键相互作用。在主沟槽中,阳离子的水配体可以通过H键与一个或相邻碱基的O和N原子相互作用,此外,较软的Ca(2+)可以形成极性共价键,桥接相邻的N7和O6原子, GG基地。由于先前概述的原因,既没有预期也没有发现局部单价阳离子。超高原子分辨率提供了DNA两条沟槽中水合的前所未有的视图,允许分析各个各向异性的位移参数,并且每个DNA双链体最多显示22个二价阳离子。每个DNA螺旋都是非常各向异性的,并且观察到糖-磷酸骨架的交替构象,沿着打开和关闭小凹槽的方向运动。考虑到这四个螺旋和其他24个Mg(2+)和Ca(2+)结合的B-DNA结构之间的实验参数和晶体堆积环境的变异性,我们得出结论,Mg的序列特异性和链特异性结合(2+)和Ca(2+)到大沟导致DNA弯曲通过基辊向大沟压缩,而Mg(2+)和Ca(2+)在小沟中的序列特异性结合具有对螺旋曲率的影响可忽略不计。较小的凹槽可以打开和关闭,以容纳Mg(2+)和Ca(2+),而不必对整个螺旋线进行明显弯曲。编写了Shelxdna程序,以帮助通过Shelxl-97精制和分析X射线晶体并绘制和分析一个或多个Curves和Freehelix输出文件。版权所有2000学术出版社。

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