Use of Spectroscopic, Zeta Potential and Molecular Dynamic Techniques to Study the Interaction between Human Holo-Transferrin and Two Antagonist Drugs:Comparison of Binary and Ternary Systems

被引:78
作者
Kabiri, Mona [1 ]
Amiri-Tehranizadeh, Zeinab [2 ]
Baratian, Ali [2 ]
Saberi, Mohammad Reza [2 ]
Chamani, Jamshidkhan [1 ]
机构
[1] Islamic Azad Univ, Dept Biol, Fac Sci, Mashhad Branch, Mashhad 9175687119, Iran
[2] Mashhad Univ Med Sci, Dept Med Chem, Sch Pharm, Mashhad 9175687119, Iran
关键词
human holo-transferrin; ropinirole hydrochloride; spectroscopic techniques; zeta potential; molecular modeling; BOVINE SERUM-ALBUMIN; PROTEIN-LIGAND INTERACTIONS; FLUORESCENCE SPECTROSCOPY; BINDING-SITES; ROPINIROLE HYDROCHLORIDE; TRYPTOPHAN FLUORESCENCE; SCATTERING TECHNIQUE; CELLULAR UPTAKE; ANION-BINDING; IRON RELEASE;
D O I
10.3390/molecules17033114
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
For the first time, the binding of ropinirole hydrochloride (ROP) and aspirin (ASA) to human holo- transferrin (hTf) has been investigated by spectroscopic approaches (fluorescence quenching, synchronous fluorescence, time-resolved fluorescence, three-dimensional fluorescence, UV-vis absorption, circular dichroism, resonance light scattering), as well as zeta potential and molecular modeling techniques, under simulated physiological conditions. Fluorescence analysis was used to estimate the effect of the ROP and ASA drugs on the fluorescence of hTf as well as to define the binding and quenching properties of binary and ternary complexes. The synchronized fluorescence and three-dimensional fluorescence spectra demonstrated some micro-environmental and conformational changes around the Trp and Tyr residues with a faint red shift. Thermodynamic analysis displayed the van der Waals forces and hydrogen bonds interactions are the major acting forces in stabilizing the complexes. Steady-state and time- resolved fluorescence data revealed that the fluorescence quenching of complexes are static mechanism. The effect of the drugs aggregating on the hTf resulted in an enhancement of the resonance light scattering (RLS) intensity. The average binding distance between were computed according to the forster non-radiation energy transfer theory. The circular dichroism (CD) spectral examinations indicated that the binding of the drugs induced a conformational change of hTf. Measurements of the zeta potential indicated that the combination of electrostatic and hydrophobic interactions between ROP, ASA and hTf formed micelle-like clusters. The molecular modeling confirmed the experimental results. This study is expected to provide important insight into the interaction of hTf with ROP and ASA to use in various toxicological and therapeutic processes.
引用
收藏
页码:3114 / 3147
页数:34
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