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将一个庞大的铑配合物插入DNA胞嘧啶-胞嘧啶错配中:核磁共振溶液研究

Insertion of a bulky rhodium complex into a DNA cytosine-cytosine mismatch: an NMR solution study.

作者信息

Cordier Christine, Pierre Valérie C, Barton Jacqueline K

机构信息

Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, California 91125, USA.

出版信息

J Am Chem Soc. 2007 Oct 10;129(40):12287-95. doi: 10.1021/ja0739436. Epub 2007 Sep 18.

Abstract

The bulky octahedral complex Rh(bpy)2chrysi3+ (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)2chrysi3+ 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 C2'-endo conformation. Remarkably, 31P 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.

摘要

庞大的八面体配合物Rh(bpy)2chrysi3+(chrysi = 5,6-苯并菲醌二亚胺)以微摩尔级的结合亲和力和高选择性结合DNA双链体中的单碱基错配。在此,我们进行了一项核磁共振溶液研究,以表征这种庞大金属配合物与其在寡核苷酸双链体(5'-CGGACTCCG-3')2中的目标CC错配的结合模式。NOESY和COSY研究均表明,Rh(bpy)2chrysi3+通过小沟在错配位点深深插入DNA,并将两个不稳定的胞嘧啶排入相对的大沟。这种插入仅对结合位点局部的寡核苷酸构象产生最小程度的扭曲。两侧匹配良好的碱基对彼此仍保持紧密的氢键结合,二维DQF-COSY实验表明所有糖均保持其原始的C2'-内型构象。值得注意的是,31P NMR显示磷酸角从BI构象转变为BII构象足以使庞大的金属配合物插入。这些结果证实了通过晶体学获得的结果,并且重要的是,为溶液中的这种特定插入模式提供了结构证据。

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