Labiuk Shaunivan L, Delbaere Louis T J, Lee Jeremy S
Department of Biochemistry, University of Saskatchewan, 107 Wiggins Road, S7N 5E5, Saskatoon, SK, Canada.
J Biol Inorg Chem. 2003 Sep;8(7):715-20. doi: 10.1007/s00775-003-0473-4. Epub 2003 Jul 9.
Three novel X-ray crystal structures for the DNA hexamer d(GGCGCC) in the B-form complexed to divalent cobalt, nickel and zinc ions have been determined to a resolution of 2.9-3.0 A. The structures were isomorphous and had five DNA strands and five metal cations per asymmetric unit. In all three cases, divalent metal cations were coordinated only to the terminal guanine residue at the N(7) position, with no metal ions binding to non-terminal guanine positions. Water molecules bound to the metal cations interacted with neighboring guanine residues 3' to the ones to which the cations were coordinated, affecting the propeller twist. Even though DNA occupied only about 35% of the unit cell volume, it is interesting that the few interactions involving the metal cations were sufficient to stabilize the crystal lattice. As well as lending support to the proposal that these metals do not coordinate to B-DNA in a stable manner, the results presented here also extend the crystallographic evidence for this phenomenon to the GGC and CGC sequences for all three metal cations.
已确定了与二价钴、镍和锌离子复合的B型DNA六聚体d(GGCGCC)的三种新型X射线晶体结构,分辨率达到2.9 - 3.0埃。这些结构是同晶型的,每个不对称单元有五条DNA链和五个金属阳离子。在所有三种情况下,二价金属阳离子仅与末端鸟嘌呤残基的N(7)位置配位,没有金属离子与非末端鸟嘌呤位置结合。与金属阳离子结合的水分子与阳离子配位的鸟嘌呤残基3'侧的相邻鸟嘌呤残基相互作用,影响螺旋桨扭转。尽管DNA仅占据单位晶胞体积的约35%,但有趣的是,涉及金属阳离子的少数相互作用足以稳定晶格。除了支持这些金属不能以稳定方式与B - DNA配位的提议外,此处给出的结果还将这一现象的晶体学证据扩展到了所有三种金属阳离子的GGC和CGC序列。