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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.
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页码:85 / 94
页数:10
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