Nguyen Thi Quynh Ngoc, Lim Kah Wai, Phan Anh Tuân
School of Physical and Mathematical Sciences, Nanyang Technological University, Singapore, Singapore.
Sci Rep. 2017 Sep 20;7(1):11969. doi: 10.1038/s41598-017-10583-9.
Small-molecule ligands targeting nucleic acids have been explored as potential therapeutic agents. Duplex groove-binding ligands have been shown to recognize DNA in a sequence-specific manner. On the other hand, quadruplex-binding ligands exhibit high selectivity between quadruplex and duplex, but show limited discrimination between different quadruplex structures. Here we propose a dual-specific approach through the simultaneous application of duplex- and quadruplex-binders. We demonstrated that a quadruplex-specific ligand and a duplex-specific ligand can simultaneously interact at two separate binding sites of a quadruplex-duplex hybrid harbouring both quadruplex and duplex structural elements. Such a dual-specific targeting strategy would combine the sequence specificity of duplex-binders and the strong binding affinity of quadruplex-binders, potentially allowing the specific targeting of unique quadruplex structures. Future research can be directed towards the development of conjugated compounds targeting specific genomic quadruplex-duplex sites, for which the linker would be highly context-dependent in terms of length and flexibility, as well as the attachment points onto both ligands.
靶向核酸的小分子配体已被探索作为潜在的治疗剂。双链沟槽结合配体已被证明以序列特异性方式识别DNA。另一方面,四链体结合配体在四链体和双链体之间表现出高选择性,但在不同四链体结构之间的区分能力有限。在这里,我们提出了一种通过同时应用双链体和四链体结合剂的双特异性方法。我们证明,一种四链体特异性配体和一种双链体特异性配体可以同时在一个包含四链体和双链体结构元件的四链体-双链体杂交体的两个独立结合位点相互作用。这种双特异性靶向策略将结合双链体结合剂的序列特异性和四链体结合剂的强结合亲和力,有可能实现对独特四链体结构的特异性靶向。未来的研究可以朝着开发靶向特定基因组四链体-双链体位点的共轭化合物的方向进行,对于这种化合物,连接子在长度和灵活性以及与两种配体的连接点方面将高度依赖于具体情况。