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

Bioorg Med Chem Lett

Division of Medicinal Chemistry, College of Pharmacy, The University of Texas at Austin, 78712, Austin, TX 78712, USA.

Published: February 2002

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.

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http://dx.doi.org/10.1016/s0960-894x(01)00775-2DOI Listing

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