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DNA variability in five crystal structures of d(CGCAATTGCG).

机译:d(CGCAATTGCG)的五个晶体结构中的DNA变异性。

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摘要

The deoxyoligonucleotide d(CGCAATTGCG) has previously been crystallized in four different space groups. The crystals diffract to moderate resolution (2.3-2.9 A). Here, a fifth crystal form that diffracts to higher resolution (1.6 A) is presented which was obtained thanks to the use of Co2+ and cryogenic temperatures. The availability of five different crystal structures allows a thorough analysis of the conformational variability of this DNA sequence. It is concluded that the central hexamer sequence CAATTG has a practically constant conformation under all conditions, whilst the terminal base pairs at both ends vary considerably as a result of differing interactions in the crystals. The new crystal structure presented here is stabilized by guanine-Co2+-guanine interactions and the formation of C1+ -G8.C3 triplexes between neighbouring duplexes. As a result of the higher resolution of the crystal structure, a more regular structure was obtained and a clear definition of the spine of hydration was observed which was not visible in the four previous structures.
机译:脱氧寡核苷酸d(CGCAATTGCG)先前已在四个不同的空间组中结晶。晶体衍射至中等分辨率(2.3-2.9 A)。在这里,呈现了衍射到更高分辨率(1.6 A)的第五种晶型,这是由于使用了Co2 +和低温而获得的。五个不同晶体结构的可用性允许对该DNA序列的构象变异性进行全面分析。结论是中心六聚体序列CAATTG在所有条件下均具有几乎恒定的构象,而由于晶体中不同相互作用的结果,两端的末端碱基对也相差很大。此处显示的新晶体结构通过鸟嘌呤-Co2 +-鸟嘌呤相互作用和相邻双链体之间C1 + -G8.C3三元组的形成而稳定。由于晶体结构的分辨率较高,因此获得了更规则的结构,并且观察到水合脊柱的清晰定义,而这在先前的四个结构中是不可见的。

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