Djuran Milos I, Milinkovic Snezana U, Habtemariam Abraha, Parsons Simon, Sadler Peter J
Department of Chemistry, University of Kragujevac, R. Domanovica 12, P.O. Box 60, 34000 Kragujevac, Yugoslavia.
J Inorg Biochem. 2002 Feb;88(3-4):268-73. doi: 10.1016/s0162-0134(01)00351-8.
We have synthesised the complex [Pt(CH(3)SCH(2)CH(2)SCH(3))(5'-GMP-N7)(2)].6H(2)O (1), where 5'-GMP is 5'-guanosine monophosphate, and determined its X-ray crystal structure. Pt(II) adopts a square-planar geometry in which the bases are coordinated head-to-tail (HT) in the Delta configuration. The nucleotide conformation in this complex is almost identical to that in the previously reported complex [Pt(en)(5'-GMP-N7)(2)].9H(2)O (2), in which there is outer sphere macrochelation via intramolecular H-bonding between the monoanionic phosphate groups and the coordinated ethylenediamine (en) NH. It is therefore apparent that intermolecular interactions rather than intramolecular H-bonding determines the orientation of the sugar-phosphate side-chain in these Pt(II) bisnucleotide complexes in the solid state.
我们合成了配合物[Pt(CH(3)SCH(2)CH(2)SCH(3))(5'-GMP-N7)(2)].6H(2)O(1),其中5'-GMP为5'-鸟苷单磷酸,并测定了其X射线晶体结构。Pt(II)采用平面正方形几何构型,其中碱基以Δ构型头对头(HT)配位。该配合物中的核苷酸构象与先前报道的配合物[Pt(en)(5'-GMP-N7)(2)].9H(2)O(2)几乎相同,在配合物(2)中,单阴离子磷酸基团与配位的乙二胺(en)NH之间通过分子内氢键形成外层大环螯合。因此,很明显,在固态下,这些Pt(II)双核苷酸配合物中糖-磷酸侧链的取向是由分子间相互作用而非分子内氢键决定的。