Surfactant-cobalt(III) complexes: The impact of hydrophobicity on interaction with HSA and DNA - insights from experimental and theoretical approach

被引:34
作者
Veeralakshmi, Selvakumar [1 ]
Sabapathi, Gopal [1 ]
Nehru, Selvan [1 ,2 ]
Venuvanalingam, Ponnambalam [1 ]
Arunachalam, Sankaralingam [1 ]
机构
[1] Bharathidasan Univ, Sch Chem, Tiruchirappalli 620024, Tamil Nadu, India
[2] Univ Madras, Sch Chem Sci, Dept Phys Chem, Guindy Campus, Chennai 600025, Tamil Nadu, India
关键词
Surfactant-cobalt(III) complexes; Hydrophobicity; HSA and DNA binding; DFT and molecular docking; Electrostatic and hydrophobic interactions; Groove binding and partial intercalation; BOVINE SERUM-ALBUMIN; BINDING INTERACTION; FLUORESCENCE SPECTROSCOPY; ETHIDIUM-BROMIDE; SINGLE; ACID; BSA;
D O I
10.1016/j.colsurfb.2017.02.013
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
To develop surfactant-based metallodrugs, it is very important to know about their hydrophobicity, micelle forming capacity, their interaction with biomacromolecules such as proteins and nucleic acids, and biological activities. Here, diethylenetriamine (dien) and tetradecylamine ligand (TA) based surfactant-cobalt(III) complexes with single chain domain, [Co(dien)(TA)Cl-2]ClO4 (1) and double chain domain [Co(dien)(TA)(2)(Cl](ClO4)(2) (2) were chosen to study the effect of hydrophobicity on the interaction with human serum albumin and calf thymus DNA. The obtained results showed that (i) single chain surfactant-cobalt(III) complex (1) interact with HSA and DNA via electrostatic interaction and groove binding, respectively; (ii) double chain surfactant-cobalt(III) complex (2) interact with HSA and DNA via hydrophobic interaction and partial intercalation, respectively, due to the play of hydrophobicity by single and double chain domains. Further it is noted that, double chain surfactant-cobalt(III) complex interact strongly with HSA and DNA, compared single chain surfactant-cobalt(III) complex due to their more hydrophobicity nature. DFT and molecular docking studies offer insights into the mechanism and mode of binding towards the molecular target CT-DNA and HSA. Hence, the present findings will create new avenue towards the use of hydrophobic metallodrugs for various therapeutic applications. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:85 / 94
页数:10
相关论文
共 53 条
[1]  
[Anonymous], J BIOMOL STRUCT DYN
[2]  
[Anonymous], PRINCIPLES FLUORESCE
[3]   Interaction studies of a novel Co(II)-based potential chemotherapeutic agent with human serum albumin (HSA) employing biophysical techniques [J].
Arjmand, Farukh ;
Tewatia, Poonam ;
Aziz, Mubashira ;
Khan, Rizwan H. .
MEDICINAL CHEMISTRY RESEARCH, 2010, 19 (08) :794-807
[4]   QUENCHING OF DNA-ETHIDIUM FLUORESCENCE BY AMSACRINE AND OTHER ANTITUMOR AGENTS - A POSSIBLE ELECTRON-TRANSFER EFFECT [J].
BAGULEY, BC ;
LEBRET, M .
BIOCHEMISTRY, 1984, 23 (05) :937-943
[5]   A SPECTROPHOTOMETRIC INVESTIGATION OF THE INTERACTION OF IODINE WITH AROMATIC HYDROCARBONS [J].
BENESI, HA ;
HILDEBRAND, JH .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1949, 71 (08) :2703-2707
[6]  
CARTER DC, 1994, ADV PROTEIN CHEM, V45, P153
[7]   Binding of Oxytetracycline to Bovine Serum Albumin: Spectroscopic and Molecular Modeling Investigations [J].
Chi, Zhenxing ;
Liu, Rutao ;
Teng, Yue ;
Fang, Xiaoyan ;
Gao, Canzhu .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2010, 58 (18) :10262-10269
[8]   VISCOSITY AND SEDIMENTATION STUDY OF SONICATED DNA-PROFLAVINE COMPLEXES [J].
COHEN, G ;
EISENBERG, H .
BIOPOLYMERS, 1969, 8 (01) :45-+
[9]   Interaction of APT with BSA or HSA [J].
Cui Fengling ;
Cui Yanrui ;
Luo Hongxia ;
Yao Xiaojun ;
Fan Jing ;
Lu Yan .
CHINESE SCIENCE BULLETIN, 2006, 51 (18) :2201-2207
[10]  
DeLano WL., 2002, PYMOL MOL GRAPHICS S