Human telomeric G-quadruplex DNA interactions of N-phenanthroline glycosylamine copper(II) complexes

被引:26
作者
Duskova, Katerina [1 ]
Sierra, Sara [1 ]
Arias-Perez, Maria-Selma [1 ]
Gude, Lourdes [1 ]
机构
[1] Univ Alcala, Dept Quim Organ Quim Inorgan, Alcala De Henares 28805, Madrid, Spain
关键词
G-quadruplex DNA; DNA interactions; 1,10-Phenanthroline; Copper(II) complexes; Glycosylamines; INTERCALATOR DISPLACEMENT ASSAY; METAL-COMPLEXES; CIRCULAR-DICHROISM; BINDING; RECOGNITION; LIGANDS; SELECTIVITY; TARGETS; VISUALIZATION; STABILITY;
D O I
10.1016/j.bmc.2015.11.037
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We report in this article the interactions of five N-(1,10-phenanthrolin-5-yl)-beta-glycopyranosylamine copper(II) complexes with G-quadruplex DNA. Specifically, the interactions of these compounds with a human telomeric oligonucleotide have been assessed by fluorescence-based assays (FRET melting and G4-FID), circular dichroism and competitive equilibrium dialysis experiments. The metal complexes bind and stabilize G-quadruplex DNA structures with apparent association constants in the order of 10(4)-10(5) M-1 and the affinity observed is dependent on the ionic conditions utilized and the specific nature of the carbohydrate moiety tethered to the 1,10-phenanthroline system. The compounds showed only a slight preference to bind G-quadruplex DNA over duplex DNA when the quadruplex DNA was folded in sodium ionic conditions. However, the binding affinity and selectivity, although modest, were notably increased when the G-quadruplex DNA was folded in the presence of potassium metal ions. Moreover, the study points towards a significant contribution of groove and/or loop binding in the recognition mode of quadruplex structures by these non-classical quadruplex ligands. The results reported herein highlight the potential and the versatility of carbohydrate bis-phenanthroline metal-complex conjugates to recognize G-quadruplex DNA structures. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:33 / 41
页数:9
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