Dipartimento di Chimica Farmaceutica e Tossicologica, Università degli Studi di Napoli Federico II, via D. Montesano 49, I-80131 Napoli, Italy.
J Am Chem Soc. 2009 Nov 18;131(45):16336-7. doi: 10.1021/ja9063662.
In the past decade, DNA G-quadruplexes have come into the limelight thanks to their biological implications and to their potential druggability in anticancer therapy. In particular, it has been found that small molecules that stabilize G-quadruplex structures are effective inhibitors of telomerase which plays a critical role in tumorigenesis. So far, the quadruplex groove recognition, which is expected to give a higher degree of selectivity over the other DNA structures, has been demonstrated for very few compounds. Thus with the aim of detecting new and structurally diverse groove binders, a structure-based virtual screening campaign has been performed using the X-ray structure of the d(TGGGGT) quadruplex. Remarkable results were achieved, and six brand new different molecular entities have been found to interact with the groove through NMR experiments. The reported results will certainly stimulate further studies aimed at the design and optimization of new quadruplex-specific groove binders to be applied as anticancer agents and for other diseases.
在过去的十年中,由于其生物学意义以及在抗癌治疗中潜在的可药性,DNA G-四链体引起了人们的关注。特别是,已经发现稳定 G-四链体结构的小分子是端粒酶的有效抑制剂,端粒酶在肿瘤发生中起着关键作用。到目前为止,已经证明了非常少数的化合物具有四链体沟槽识别能力,这有望比其他 DNA 结构具有更高的选择性。因此,为了检测新的结构多样的沟槽结合物,我们使用 [d(TGGGGT)] (4) 四链体的 X 射线结构进行了基于结构的虚拟筛选。取得了显著的结果,并通过 NMR 实验发现了六种全新的不同分子实体与沟槽相互作用。所报道的结果肯定会激发进一步的研究,旨在设计和优化新的四链体特异性沟槽结合物,作为抗癌剂和其他疾病的应用。