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Cobalt hexammine induced tautomeric shift in Z-DNA: the structure of d(CGCGCA).d(TGCGCG) in two crystal forms

机译:钴己胺诱导的Z-DNA互变异构移位:两种晶体形式的d(CGCGCA).d(TGCGCG)的结构

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摘要

We report here the crystal structure of the DNA hexamer duplex d(CGCGCA).d(TGCGCG) at 1.71 Å resolution. The crystals, in orthorhombic space group, were grown in the presence of cobalt hexammine, a known inducer of the left-handed Z form of DNA. The interaction of this ion with the DNA helix results in a change of the adenine base from the common amino tautomeric form to the imino tautomer. Consequently the A:T base pair is disrupted from the normal Watson–Crick base pairing to a ‘wobble’ like base pairing. This change is accommodated easily within the helix, and the helical parameters are those expected for Z-DNA. When the cobalt hexammine concentration is decreased slightly in the crystallization conditions, the duplex crystallizes in a different, hexagonal space group, with two hexamer duplexes in the asymmetric unit. One of these is situated on a crystallographic 6-fold screw axis, leading to disorder. The tautomeric shift is not observed in this space group. We show that the change in inter-helix interactions that lead to the two different space groups probably arise from the small decrease in ion concentration, and consequently disordered positions for the ion.
机译:我们在这里报告了1.71Å分辨率的DNA六聚体双链体d(CGCGCA).d(TGCGCG)的晶体结构。正交晶空间群中的晶体是在钴己胺存在下生长的,钴己胺是DNA左旋Z形式的已知诱导剂。该离子与DNA螺旋的相互作用导致腺嘌呤碱基从常见的氨基互变异构形式变为亚氨基互变异构体。因此,A:T碱基对从正常的Watson-Crick碱基对变为类似碱基对的“摆动”。这种变化很容易容纳在螺旋内,螺旋参数是Z-DNA所期望的。当在结晶条件下钴六乙胺的浓度略有降低时,双链体会在不同的六边形空间群中结晶,在不对称单元中有两个六聚体双链体。其中之一位于晶体学6倍螺旋轴上,导致混乱。在该空间群中未观察到互变异构移位。我们表明,导致两个不同空间组的螺旋间相互作用的变化可能是由于离子浓度的小幅下降,以及离子的无序位置引起的。

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