A study of Pt(II)-phenanthroline complex interactions with double-stranded and G-quadruplex DNA by ESI-MS, circular dichroism, and computational docking

被引:19
作者
Ang, Dale L. [1 ]
Kelso, Celine [3 ]
Beck, Jennifer L. [3 ]
Ralph, Stephen F. [3 ]
Harman, David G. [2 ]
Aldrich-Wright, Janice R. [1 ,2 ]
机构
[1] Western Sydney Univ, Nanoscale Org & Dynam Grp, Sch Sci, Penrith, NSW 2751, Australia
[2] Western Sydney Univ, Sch Med, Locked Bag 1797, Penrith, NSW 2751, Australia
[3] Univ Wollongong, Sch Chem & Mol Biosci, Northfields Ave, Wollongong, NSW 2522, Australia
来源
JOURNAL OF BIOLOGICAL INORGANIC CHEMISTRY | 2020年 / 25卷 / 03期
关键词
Platinum; Anticancer drug; Computational chemistry; Docking; Mass spectrometry; Binding affinity; G-quadruplex; MASS-SPECTROMETRY; ION SUPPRESSION; LIGAND; DERIVATIVES; BINDING;
D O I
10.1007/s00775-020-01773-4
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
The binding interactions of a series of square-planar platinum(II)-phenanthroline complexes of the type [Pt(P-L)(A(L))](2+) [where P-L = variously methyl-substituted 1,10-phenanthroline (phen) and A(L) = ethane-1,2-diamine (en)] were assessed with a G-quadruplex DNA (5 '-TTG GGG GT-3 ', G4DNA) and a double-stranded DNA (5 '-CGC GAA TTC GCG-3 ', dsDNA) sequence by ESI-MS. The results indicate a strong correlation between G4DNA affinity and increasing phenanthroline methyl substitution. Circular dichroism (CD) spectroscopy and molecular docking studies also support the finding that increased substitution of the phenanthroline ligand increased selectivity for G4DNA. Graphic abstract ESI-MS was used to probe the interaction of a range of square-planar Pt(II)-phenanthroline complexes with double-stranded and G-quadruplex DNA. [GRAPHICS] .
引用
收藏
页码:429 / 440
页数:12
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