Determination of apo-metallothionein using adsorptive transfer stripping technique in connection with differential pulse voltammetry

被引:61
|
作者
Adam, Vojtech
Krizkova, Sona
Zitka, Ondrej
Trnkova, Libuse
Petrlova, Jitka
Beklova, Miroslava
Kizek, Rene
机构
[1] Mendel Univ Brno, Fac Agron, Dept Chem & Biochem, Lab Mol Biochem & Bioelectrochem, CZ-61300 Brno, Czech Republic
[2] Masaryk Univ, Dept Genet & Mol Biol, CZ-61137 Brno, Czech Republic
[3] Masaryk Univ, Dept Biochem, CZ-61137 Brno, Czech Republic
[4] Masaryk Univ, Fac Sci, Dept Theoret & Phys Chem, CZ-61137 Brno, Czech Republic
[5] Univ Vet & Pharmaceut Sci, Fac Vet Hyg & Ecol, Dept Vet Ecol & Environm Protect, CZ-61242 Brno, Czech Republic
关键词
differential pulse voltammetry (DPV); adsorptive transfer stripping (AdTS) technique; hanging mercury; drop electrode (HMDE); metallothionein; reaction of thiol group; heavy metals biosensor; EDTA;
D O I
10.1002/elan.200603738
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Links between metallothionein (MT), its structure and many biologically important pathways demonstrate the necessity of taking into account of studying the behavior of MT in different well defined mediums, which could help to model conditions in an organism easily. The main aim of this work was to prepare and determine apoMT by adsorptive transfer stripping technique (AdTS) in connection with differential pulse voltammetry (DPV). Particularly, we investigated the electrochemical behavior of MT measured on the surface of hanging mercury drop electrode in the presence of sodium chloride as supporting electrolyte using AdTS DPV with respect to study the effects of MT signals by different concentrations and pH's of the electrolyte. Then, we aimed at utilizing this technique to observe changes in MT which are dependent on using strong chelating compounds ethylendiamine-N, N, N', N'-tetraacetic acid (EDTA). Thanks to ability of EDTA to bind heavy metals from active center of enzymes and regulation proteins, we were able to prepare apoMT; that means, MT without any metal ion bound in its structure. Detection limit of apoMT at very short time of accumulation (t(A) = 120 s) was 3 nM (20 ng/mL and/or 15 fmol in 5 mu L drop; RSD 2-5%) estimated by dilution of the analyzed solution until the signal disappeared. In addition, it was possible to decrease detection limit by extending of time of accumulation of apoMT on the surface of HMDE. We were able to detect 30 pM of apoMT (200 pg/mL and/or 150 amol in 5 mu L drop) at t(A) = 500 s.
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页码:339 / 347
页数:9
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