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Selective Recognition of G-Quadruplex Telomeric DNA by a Bis(quinacridine) Macrocycle

2003; American Chemical Society; Volume: 125; Issue: 16 Linguagem: Inglês

10.1021/ja021299j

1943-2984

Marie‐Paule Teulade‐Fichou, Carolina Carrasco, Lionel Guittat, Christian Bailly, Patrizia Alberti, Jean‐Louis Mergny, Arnaud David, Jean‐Maríe Lehn, W. David Wilson,

RNA Interference and Gene Delivery

The interaction of G-quadruplex DNA with the macrocyclic compound BOQ1, which possesses two dibenzophenanthroline (quinacridine) subunits, has been investigated by a variety of methods. The oligonucleotide 5'-A(GGGT2A)3G3, which mimics the human telomeric repeat sequence and forms an intramolecular quadruplex, was used as one model system. Equilibrium binding constants measured by biosensor surface plasmon resonance (SPR) methods indicate a high affinity of the macrocycle for the quadruplex conformation (K > 1 × 107 M-1) with two equivalent binding sites. The affinity of BOQ1 for DNA duplexes is at least 1 order of magnitude lower. In addition, the macrocycle is more selective than the monomeric control compound (MOQ2), which is not able to discriminate between the two DNA structures (Kduplex ≈ Kquadruplex ≈ 106 M-1). Strong binding of BOQ1 to G4 DNA sequences was confirmed by fluorometric titrations with a tetraplex-forming oligonucleotide. Competition dialysis experiments with a panel of different DNA structures, from single strands to quadruplexes, clearly established the quadruplex binding specificity of BOQ1. Fluorescence resonance energy transfer (FRET) Tm experiments with a doubly labeled oligonucleotide also revealed a strong stabilization of the G4 conformation in the presence of BOQ1 (ΔTm = +28 °C). This ΔTm value is one of the highest values measured for a G-quadruplex ligand and is significantly higher than observed for the monomer control compounds (ΔTm = +10−12 °C). Gel mobility shift assays indicated that the macrocycle efficiently induces the formation of G-tetraplexes. Strong inhibition of telomerase was observed in the submicromolar range (IC50 = 0.13 μM). These results indicate that macrocycles represent an exciting new development opportunity for targeting DNA quadruplexes.