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DNA结合的第三种模式:多核铂配合物形成的磷酸钳

A third mode of DNA binding: Phosphate clamps by a polynuclear platinum complex.

作者信息

Komeda Seiji, Moulaei Tinoush, Woods Kristen Kruger, Chikuma Masahiko, Farrell Nicholas P, Williams Loren Dean

机构信息

School of Chemistry and Biochemistry, Georgia Institute of Technology, Atlanta, Georgia 30332-0400, USA.

出版信息

J Am Chem Soc. 2006 Dec 20;128(50):16092-103. doi: 10.1021/ja062851y.

Abstract

We describe a 1.2 A X-ray structure of a double-stranded B-DNA dodecamer (the Dickerson Dodecamer, DDD, [d(CGCGAATTCGCG)]2) associated with a cytotoxic platinum(II) complex, [{trans-Pt(NH3)2(NH2(CH2)6(NH3+)}2-mu-{trans-Pt(NH3)2(NH2(CH2)6NH2)2}] (TriplatinNC). TriplatinNC is a multifunctional DNA ligand, with three cationic Pt(II) centers, and directional hydrogen bonding functionalities, linked by flexible hydrophobic segments, but without the potential for covalent interaction. TriplatinNC does not intercalate nor does it bind in either groove. Instead, it binds to phosphate oxygen atoms and thus associates with the backbone. The three square-planar tetra-am(m)ine Pt(II) coordination units form bidentate N...O...N complexes with OP atoms, in a motif we call the Phosphate Clamp. The geometry is conserved among the 8 observed phosphate clamps in this structure. The interaction appears to prefer O2P over O1P atoms (frequency of interaction is O2P > O1P, base and sugar oxygens > N). The high repetition and geometric regularity of the motif suggests that this type of Pt(II) center can be developed as a modular nucleic acid binding device with general utility. TriplatinNC extends along the phosphate backbone, in a mode of binding we call "Backbone Tracking" and spans the minor groove in a mode of binding we call "Groove Spanning". Electrostatic forces appear to induce modest DNA bending into the major groove. This bending may be related to the direct coordination of a sodium cation by a DNA base, with unprecedented inner-shell (direct) coordination of penta-hydrated sodium at the O6 atom of a guanine.

摘要

我们描述了一种双链B-DNA十二聚体(迪克森十二聚体,DDD,[d(CGCGAATTCGCG)]2)与一种细胞毒性铂(II)配合物[{反式-Pt(NH3)2(NH2(CH2)6(NH3+)}2-μ-{反式-Pt(NH3)2(NH2(CH2)6NH2)2}](三铂NC)结合的1.2埃X射线结构。三铂NC是一种多功能DNA配体,具有三个阳离子铂(II)中心和定向氢键功能,由柔性疏水链段连接,但没有共价相互作用的可能性。三铂NC既不嵌入也不在任何一条沟中结合。相反,它与磷酸氧原子结合,从而与主链缔合。三个平面正方形四胺铂(II)配位单元与OP原子形成双齿N...O...N配合物,我们将这种模式称为磷酸钳。在该结构中观察到的8个磷酸钳中,这种几何结构是保守的。这种相互作用似乎更倾向于O2P而非O1P原子(相互作用频率为O2P > O1P,碱基和糖氧> N)。该模式的高重复性和几何规则性表明,这种类型的铂(II)中心可被开发为一种具有广泛用途的模块化核酸结合装置。三铂NC沿着磷酸主链延伸,以一种我们称为“主链追踪”的结合模式跨越小沟,以一种我们称为“沟跨越”的结合模式跨越小沟。静电力似乎诱导DNA适度弯曲进入大沟。这种弯曲可能与DNA碱基对钠阳离子的直接配位有关,鸟嘌呤的O6原子对五水合钠进行了前所未有的内壳层(直接)配位。

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