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首页> 外文期刊>Inorganic Chemistry Communications >The ligand-structure-selective binding of oligonucleotide by cobalt complexes
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The ligand-structure-selective binding of oligonucleotide by cobalt complexes

机译:钴配合物对寡核苷酸的配体-结构-选择性结合

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摘要

The binding of two Co(III) complexes [Co(phen)2(DPQ)]~(3+) and [Co(phen)2(HPlP)]Cl3 [HPIP = 2-(2-hydroxy-phenyl) imidazo [4,5-f)[1,10] phenanthroline, DPQ= dipyrido[3,2-f:2',3'-h]quinoxaline] to the normal base-paired decanucleotide d(CCTAATTAGG)2 was studied by 2D NMR. The results indicate that the width of intercalating ligand has a large effect on the selectivity of binding site. For [Co(phen)2(HPIP)]Cl3, the complex binds the decanucleotide at C2T3:G9A8 and A4A5:T7T6 by intercalation from the minor groove, while [Co(phen)2(DPQ)]~(3+) intercalates into T3A4:T7A8 region from the minor groove. The conclusion was further proved by molecular modeling.
机译:两种Co(III)配合物[Co(phen)2(DPQ)]〜(3+)和[Co(phen)2(HPlP)] Cl3 [HPIP = 2-(2-羟基-苯基)咪唑[通过2D NMR研究了4,5-f)[1,10]菲咯啉,DPQ =双吡啶[3,2-f:2',3'-h]喹喔啉]与正常碱基配对十核苷酸d(CCTAATTAGG)2的关系。结果表明,嵌入配体的宽度对结合位点的选择性影响很大。对于[Co(phen)2(HPIP)] Cl3,复合物通过从小沟中插入而在C2T3:G9A8和A4A5:T7T6结合十核苷酸,而[Co(phen)2(DPQ)]〜(3+)插入从小凹槽进入T3A4:T7A8区域。通过分子建模进一步证实了该结论。

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