Paul Alexis, Sengupta Poulami, Krishnan Yamuna, Ladame Sylvain
Institut de Science et d'Ingénierie, Supramoléculaires (ISIS), Université Louis Pasteur, CNRS UMR 7006, 8 Allée Gaspard Monge, Strasbourg Cédex, France.
Chemistry. 2008;14(28):8682-9. doi: 10.1002/chem.200800605.
We describe the first G-quadruplex targeting approach that combines intercalation and hybridization strategies by investigating the interaction of a G-rich peptide nucleic acid (PNA) acridone conjugate 1 with a three-repeat fragment of the human telomere G 3 to form a hybrid PNA-DNA quadruplex that mimicks the biologically relevant (3+1) pure DNA dimeric telomeric quadruplex. Using a combination of UV and fluorescence spectroscopy, circular dichroism (CD), and mass-spectrometry, we show that PNA 1 can induce the formation of a bimolecular hybrid quadruplex even at low salt concentration upon interaction with a single-stranded three-repeat fragment of telomeric DNA. However, PNA 1 cannot invade a short fragment of B-DNA even if the latter contains a CCC motif complementary to the PNA sequence. These studies could open up new possibilities for the design of a novel generation of quadruplex ligands that target not only the external features of the quadruplex but also its central core constituted by the tetrads themselves.
我们通过研究富含鸟嘌呤的肽核酸(PNA)吖啶酮共轭物1与人端粒G3的三重复片段的相互作用,描述了第一种结合嵌入和杂交策略的G-四链体靶向方法,以形成一种模拟生物学相关的(3 + 1)纯DNA二聚体端粒四链体的杂交PNA-DNA四链体。通过结合紫外和荧光光谱、圆二色性(CD)和质谱分析,我们表明PNA 1与端粒DNA的单链三重复片段相互作用时,即使在低盐浓度下也能诱导形成双分子杂交四链体。然而,PNA 1不能侵入B-DNA的短片段,即使后者包含与PNA序列互补的CCC基序。这些研究可能为设计新一代四链体配体开辟新的可能性,这些配体不仅靶向四链体的外部特征,还靶向由四联体本身构成的中心核心。