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钌(II)混合配体配合物的光裂解、DNA结合、细胞毒性及对接研究

Studies on Photocleavage, DNA Binding, Cytotoxicity, and Docking Studies of Ruthenium(II) Mixed Ligand Complexes.

作者信息

Kumar Yata Praveen, Devi C Shobha, Srishailam A, Deepika N, Kumar V Ravi, Reddy P Venkat, Nagasuryaprasad K, Singh Surya S, Nagababu Penumaka, Satyanarayana S

机构信息

Department of Chemistry, Osmania University, Hyderabad, India.

School of Chemistry, University of Hyderabad, Hyderabad, India.

出版信息

J Fluoresc. 2016 Nov;26(6):2119-2132. doi: 10.1007/s10895-016-1908-y. Epub 2016 Sep 2.

Abstract

This article describes the synthesis and characterization of three new Ru(II) polypyridyl complexes including [Ru(phen)(dpphz)] (1), [Ru(bpy)(dpphz)] (2) and [Ru(dmb)(dpphz)] (3) where dpphz = dipyrido[3,2-a:2',3'-c] phenazine-11-hydrazide, phen =1,10-phenanthroline, bpy = 2,2'-bipyridine and dmb = 4,4'-dimethyl2,2'-bipyridine. The binding behaviors of these complexes to calf thymus DNA (CT-DNA) were explored by spectroscopic titrations, viscosity measurements. Results suggest that these complexes can bind to CT-DNA through intercalation. However, their binding strength differs from each other; this may be attributed to difference in the ancillary ligand. The cytotoxicity of 1-3 was evaluated by MTT assay; results indicated that all complexes have significant dose dependent cytotoxicity with HeLa tumor cell line. All complexes exhibited efficient photocleavage of pBR322 DNA upon irradiation. The DNA binding ability of 1-3 was also studied by docking the complexes into B-DNA using docking program.

摘要

本文描述了三种新型钌(II)多吡啶配合物的合成与表征,包括[Ru(phen)(dpphz)](1)、[Ru(bpy)(dpphz)](2)和[Ru(dmb)(dpphz)](3),其中dpphz = 二吡啶并[3,2-a:2',3'-c]吩嗪-11-酰肼,phen = 1,10-菲咯啉,bpy = 2,2'-联吡啶,dmb = 4,4'-二甲基-2,2'-联吡啶。通过光谱滴定、粘度测量等方法研究了这些配合物与小牛胸腺DNA(CT-DNA)的结合行为。结果表明,这些配合物可通过嵌入作用与CT-DNA结合。然而,它们的结合强度彼此不同;这可能归因于辅助配体的差异。通过MTT法评估了1-3的细胞毒性;结果表明,所有配合物对HeLa肿瘤细胞系均具有显著的剂量依赖性细胞毒性。所有配合物在光照下均能有效光切割pBR322 DNA。还使用对接程序将配合物对接至B-DNA中,研究了1-3的DNA结合能力。

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