Interaction of metal ions and DNA films on gold surfaces: an electrochemical impedance study

被引：31

作者：

Bin, Xiaomin ^{[1
]}

Kraatz, Heinz-Bernhard ^{[1
]}

机构：

[1] Univ Western Ontario, Dept Chem, London, ON N6A 5B7, Canada

来源：

ANALYST | 2009年 / 134卷 / 07期

基金：

加拿大自然科学与工程研究理事会;

关键词：

SELF-ASSEMBLED MONOLAYERS; SINGLE-NUCLEOTIDE MISMATCHES; BASE-PAIRS; CATION INTERACTIONS; NATIVE DNA; HG-II; BINDING; DUPLEX; THERMODYNAMICS; ALUMINUM(III);

D O I：

10.1039/b821670c

中图分类号：

O65 [分析化学];

学科分类号：

070302 ; 081704 ;

摘要：

Electrochemical impedance spectroscopy ( EIS) has been used to investigate the effects of a number of metal ions with DNA films on gold surfaces exploiting [Fe(CN)(6)](3-/4-) as a solution-based redox probe. Alkaline earth metal ions Mg2+, Ca2+, trivalent Al3+, La3+ and divalent transition metal ions Ni2+, Cu2+, Cd2+ and Hg2+ have been selected in this study and the results are compared with previous studies on the effects of Zn2+ on the EIS of DNA films. All experimental results were evaluated with the help of equivalent circuits which allowed the extraction of resistive and capacitive components. For all metal ions studied here, addition of the metal ions causes a decrease in the charge transfer resistance. The difference of charge transfer resistance (Delta R-ct) of ds-DNA films in the presence and absence of the various metal ions is different and particular to any given metal ion. In addition, we studied the EIS of ds-DNA films containing a single A-C mismatch in the presence and absence of Ca2+, Zn2+, Cd2+ and Hg2+.Delta R-ct values for ds-DNA films with a single A-C mismatch is smaller than those of fully matched ds-DNA films.

引用

页码：1309 / 1313

页数：5

共 44 条

[1] Geometry and electronic structure of M-DNA (M=Zn2+, Co2+, and Fe2+) [J].

Alexandre, Simone S. ;

Soler, Jose M. ;

Seijo, Luis ;

Zamora, Felix .

PHYSICAL REVIEW B, 2006, 73 (20)

[2] Metal-DNA interactions [J].

Anastassopoulou, J .

JOURNAL OF MOLECULAR STRUCTURE, 2003, 651 :19-26

[3]

Bard A.J., 2001, ELECTROCHEMICAL METH

[4] Electrochemical and surface study of ferrocenoyl oligopeptides [J].

Bediako-Amoa, I ;

Sutherland, TC ;

Li, CZ ;

Silerova, R ;

Kraatz, HB .

JOURNAL OF PHYSICAL CHEMISTRY B, 2004, 108 (02) :704-714

[5] Interaction of DNA base pairs with various metal cations (Mg2+, Ca2+, Sr2+, Ba2+, Cu+, Ag+, Au+, Zn2+, Cd2+, and Hg2+): Nonempirical ab initio calculations on structures, energies, and nonadditivity of the interaction [J].

Burda, JV ;

Sponer, J ;

Leszczynski, J ;

Hobza, P .

JOURNAL OF PHYSICAL CHEMISTRY B, 1997, 101 (46) :9670-9677

[6] SEQUENCE SELECTIVE COORDINATION OF MG2+(AQ) TO DNA [J].

COWAN, JA ;

HUANG, HW ;

HSU, LY .

JOURNAL OF INORGANIC BIOCHEMISTRY, 1993, 52 (02) :121-129

[7] Towards metalated DNA-based structures [J].

Di Felice, R ;

Calzolari, A ;

Zhang, H .

NANOTECHNOLOGY, 2004, 15 (09) :1256-1263

[8] Effect of hexacyanoferrate(II/III) on self-assembled monolayers of thioctic acid and 11-mercaptoundecanoic acid on gold [J].

Dijksma, M ;

Boukamp, BA ;

Kamp, B ;

van Bennekom, WP .

LANGMUIR, 2002, 18 (08) :3105-3112

[9] DNA-cation interactions: Quo vadis? [J].

Egli, M .

CHEMISTRY & BIOLOGY, 2002, 9 (03) :277-286

[10]

FUENTE M, 2004, J BIOL INORG CHEM, V9, P973

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