Probing the Strength and Mechanism of Binding Between Amifampridine and Calf Thymus DNA

被引:5
|
作者
Sharifinia, Samira [1 ]
Hajibabaei, Farshid [1 ]
Salehzadeh, Sadegh [1 ]
Hosseinpour Moghadam, Neda [2 ]
Khazalpour, Sadegh [1 ]
机构
[1] Bu Ali Sina Univ, Fac Chem, Hamadan 65178, Hamadan, Iran
[2] Hamadan Univ Med Sci, Res Ctr Mol Med, Hamadan 65178, Hamadan, Iran
关键词
amifampridine; DNA interaction; molecular docking; CD; DPV; intercalation; MOLECULAR DOCKING; ANTIVIRAL DRUG; IN-VITRO; MODE; COMPLEXES; CYTOTOXICITY; CLEAVAGE; LIGAND; SITE; HSA;
D O I
10.1089/dna.2020.5618
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
In this work, we have investigated the strength and mechanism of amifampridine (3,4-Diaminopyridine/3,4-DAP) interaction with calf thymus DNA (ct-DNA). The existence and the strength of interaction are evaluated using circular dichroism (CD), UV-vis absorption, and differential pulse voltammogram studies. Results from UV-vis absorption technique indicate that amifampridine can significantly interact with DNA through a binding constant ofK(b) = 1.66 x 10(5)M(-1)at 298 K. The mechanism of the interaction between amifampridine and DNA is also studied using ionic effect investigations, competitive fluorescence experiments, viscosity measurements, and molecular docking studies. The viscosity results indicate that amifampridine can bind to DNA via intercalation binding mode. Competitive fluorescence experiments using Acridine Orange (AO) and Hoechst 33258 (HO) probes also reveal that amifampridine binds to DNA via an intercalation mode of binding. Finally, the molecular docking studies also suggest that amifampridine tends to bind with the G-C rich region of DNA.
引用
收藏
页码:2134 / 2142
页数:9
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