Department of Chemistry, RGUKT, Basar, Telangana State, India.
Inorganic & Physical Chemistry Division, CSIR-Indian Institute of Chemical Technology, Uppal Road, Tarnaka, Hyderabad, 500007, Telangana State, India.
J Fluoresc. 2017 Nov;27(6):2119-2130. doi: 10.1007/s10895-017-2151-x. Epub 2017 Aug 22.
This review describes the analytical techniques used to detect DNA-probes such as Ru(II) complexes with hetero cyclic imidazo phenanthroline (IP) ligands. Studies on drug-DNA interactions are useful biochemical techniques for visualization of DNA both in vitro and in vivo. The interactions of small molecules that binds to DNA are mainly classified into two major classes, one involving covalent binding and another non-covalent binding. Covalent binding in DNA can be irreversible and may leads to inhibition of all DNA processes which subsequently leads to cell death. Usually, covalent interactions leads to permanent changes in the structure of nucleic acids. The non-covalent interaction of molecules with DNA can be due to electrostatic interaction, intercalation and groove binding. These interactions of DNA probes can be explored by various spectroscopic techniques viz. UV-visible, emission, emission quenching spectroscopy, viscosity and thermal denaturation measurements.
本文综述了用于检测 DNA 探针的分析技术,例如与杂环咪唑并菲咯啉 (IP) 配体结合的 Ru(II) 配合物。药物-DNA 相互作用的研究是体外和体内可视化 DNA 的有用生化技术。与 DNA 结合的小分子的相互作用主要分为两类,一类涉及共价键合,另一类涉及非共价键合。DNA 中的共价键合可能是不可逆的,并且可能导致所有 DNA 过程的抑制,从而导致细胞死亡。通常,共价相互作用会导致核酸结构的永久性变化。分子与 DNA 的非共价相互作用可能是由于静电相互作用、嵌入和沟结合。可以通过各种光谱技术,例如 UV-可见、发射、发射猝灭光谱、粘度和热变性测量来探索 DNA 探针的这些相互作用。