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Insertion of a Bulky Rhodium Complex into a DNA Cytosine-Cytosine Mismatch: An NMR Solution Study

机译:大块铑络合物插入DNA胞嘧啶-胞嘧啶错配:NMR解决方案研究。

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The bulky octahedral complex Rh(bpy)_2chrysi~(3+) (chrysi = 5,6-chrysenequinonediimine) binds single-base mismatches in a DNA duplex with micromolar binding affinities and high selectivity. Here we present an NMR solution study to characterize the binding mode of this bulky metal complex with its target CC mismatch in the oligonucleotide duplex (5'-CGGACTCCG-3')_2. Both NOESY and COSY studies indicate that Rh(bpy)_2chrysi~(3+) inserts deeply in the DNA at the mismatch site via the minor groove and with ejection of both destabilized cytosines into the opposite major groove. The insertion only minimally distorts the conformation of the oligonucleotide local to the binding site. Both flanking, well-matched base pairs remain tightly hydrogen-bonded to each other, and 2D DQF-COSY experiments indicate that all sugars maintain their original Cr-endo conformation. Remarkably, ~(31)P NMR reveals that opening of the phosphate angles from a BⅠ to a BⅡ conformation is sufficient for insertion of the bulky metal complex. These results corroborate those obtained crystallographically and, importantly, provide structural evidence for this specific insertion mode in solution.
机译:庞大的八面体复合体Rh(bpy)_2chrysi〜(3+)(chrysi = 5,6-chsenequinonediimine)以微摩尔结合亲和力和高选择性结合DNA双链体中的单碱基错配。在这里,我们提出了NMR解决方案研究,以表征这种庞大的金属配合物的结合模式及其在寡核苷酸双链体(5'-CGGACTCCG-3')_ 2中的目标CC错配。 NOESY和COZY的研究均表明Rh(bpy)_2chrysi〜(3+)经由小沟在错配位点深处插入DNA中,并且两种不稳定的胞嘧啶均喷射到相反的大沟中。插入仅最小化结合位点局部的寡核苷酸的构象。两侧的,匹配良好的碱基对彼此之间保持紧密的氢键结合,二维DQF-COSY实验表明,所有糖都保持其原始的Cr-endo构象。值得注意的是,〜(31)P NMR表明,从BⅠ到BⅡ构象的磷酸角的打开足以插入大块的金属配合物。这些结果证实了通过晶体学获得的结果,重要的是,为溶液中这种特定的插入模式提供了结构证据。

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