Perylene diimide G-quadruplex DNA binding selectivity is mediated by ligand aggregation

被引:76
作者
Kerwin, SM [1 ]
Chen, G [1 ]
Kern, JT [1 ]
Thomas, PW [1 ]
机构
[1] Univ Texas, Coll Pharm, Div Med Chem, Austin, TX 78712 USA
关键词
D O I
10.1016/S0960-894X(01)00775-2
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Two N,N'-disubstituted perylene diimide G-quadruplex DNA ligands, PIPER [N,N'-bis-(2-(1-piperidino)ethyl)-3,4,9,10-perylene tetracarboxylic acid diimide] and Tel01 [N,N'-bis-(3-(4-morpholino)-propyl)-3,4,9,10-perylene tetracarboxylic acid diimide] were studied. Visible absorbance, resonance light scattering, and fluorescence spectroscopy were used to characterize the pH-dependent aggregation of these ligands. The G-quadruplex DNA binding selectivity of these ligands as monitored by absorption spectroscopy is also pH-dependent. The ligands bind to both duplex and G-quadruplex DNA under low pH conditions, where the ligands are not aggregated. At higher pH, where the ligands are extensively aggregated, the apparent G-quadruplex DNA binding selectivity is high. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:447 / 450
页数:4
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