An electrochemical study of neutral red-DNA interaction

被引:25
作者
Heli, H
Bathaie, SZ
Mousavi, MF
机构
[1] Tarbiat Modarres Univ, Fac Sci, Dept Chem, Tehran, Iran
[2] Tarbiat Modarres Univ, Fac Med Sci, Dept Clin Biochem, Tehran, Iran
关键词
neutral red; calf thymus DNA; interaction; binding isotherm; impedance spectroscopy;
D O I
10.1016/j.electacta.2005.05.055
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Electrochemical methods were used to investigate the interaction of neutral red (NR) with double-stranded calf thymus DNA, in solution as well as using a DNA-modified glassy carbon (GC-DNA) electrode. The results were compared with those obtained from bare glassy carbon (GC) electrode. The formal potential of NR was more positive when GC-DNA electrode was used although the rate of heterogeneous electron transfer is as high as that of using GC electrode. GC-DNA electrode enables preconcentration of NR for chosen times on the electrode surface, despite the fact that the mass transfer effects in the thin DNA layer adsorbed on the surface was still observed using cyclic voltammetry and electrochemical impedance spectroscopy techniques. Parameters, such as the diffusion coefficient of NR, binding site size in base pairs and the ratio of the binding constants for the oxidized and reduced forms of the bound species were obtained. A binding isotherm for NR at GC-DNA electrode was obtained from coulometric titrations and gave an affinity constant equal to 2.76 x 10(4) L mol(-1). From the studies of the interaction in solution, the diffusion coefficient of free and DNA-bound NR, binding constant and binding site size of the DNA-NR complex was also obtained simultaneously by non-linear fitting analysis of voltammetric data. (C) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1108 / 1116
页数:9
相关论文
共 54 条
[1]  
Aminzadeh A, 2003, IRAN J CHEM CHEM ENG, V22, P9
[2]   Studies on mechanism of 8-methoxypsoralen - DNA interaction in the dark [J].
Arabzadeh, A ;
Bathaie, SZ ;
Farsam, H ;
Amanlou, M ;
Saboury, AA ;
Shockravi, A ;
Moosavi-Movahedi, AA .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2002, 237 (1-2) :47-55
[3]  
Bard A. J., 2001, ELECTROCHEMICAL METH
[4]   A mechanistic study of the histone H1-DNA complex dissociation by sodium dodecyl sulfate [J].
Bathaie, SZ ;
Moosavi-Movahedi, AA ;
Ranjbar, B ;
Saboury, AA .
COLLOIDS AND SURFACES B-BIOINTERFACES, 2003, 28 (01) :17-25
[5]   Energetic and binding properties of DNA upon interaction with dodecyl trimethylammonium bromide [J].
Bathaie, SZ ;
Moosavi-Movahedi, AA ;
Saboury, AA .
NUCLEIC ACIDS RESEARCH, 1999, 27 (04) :1001-1005
[6]   DYE-MODIFIED ELECTRODES FOR PHOTOGALVANIC CELLS [J].
BAULDREAY, JM ;
ARCHER, MD .
ELECTROCHIMICA ACTA, 1983, 28 (11) :1515-1522
[7]   DNA binding mode and sequence specificity of piperazinylcarbonyloxyethyl derivatives of anthracene and pyrene [J].
Becker, HC ;
Nordén, B .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1999, 121 (51) :11947-11952
[8]   Theoretical models for ac impedance of finite diffusion layers exhibiting low frequency dispersion [J].
Bisquert, J ;
Garcia-Belmonte, G ;
Fabregat-Santiago, F ;
Bueno, PR .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1999, 475 (02) :152-163
[9]   Theory of the electrochemical impedance of anomalous diffusion [J].
Bisquert, J ;
Compte, A .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 2001, 499 (01) :112-120
[10]   Mutation detection by electrocatalysis at DNA-modified electrodes [J].
Boon, EM ;
Ceres, DM ;
Drummond, TG ;
Hill, MG ;
Barton, JK .
NATURE BIOTECHNOLOGY, 2000, 18 (10) :1096-1100