Electrochemistry of immobilized CuZnSOD and FeSOD and their interaction with superoxide radicals

被引:64
作者
Ge, B [1 ]
Scheller, FW [1 ]
Lisdat, F [1 ]
机构
[1] Univ Potsdam, Inst Biochem & Biol, D-14476 Golm, Germany
关键词
copper zinc superoxide dismutase; iron-containing superoxide dismutase; superoxide radical; modified gold electrode;
D O I
10.1016/S0956-5663(02)00174-4
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Copper, zinc superoxide dismutase (CuZnSOD) from bovine erythrocytes and iron superoxide dismutase from Escherichia coli (FeSOD) were immobilized on 3-mercaptopropionic acid (MPA)-modified gold electrodes, respectively. The characterization of the SOD electrodes showed a quasi-reversible, electrochemical redox behavior with a formal potential of 47 +/- 4 mV and - 154 +/- 5 mV (vs. Ag/AgCl, 1 M KCl) for surface adsorbed CuZnSOD and FeSOD, respectively. The heterogeneous electron transfer rate constants were determined to be about 65 and 35/s, respectively. Covalent fixation of both SODs was also feasible with only slight changes in the formal potential. The interaction of superoxide radicals (O-2(-)) with the SOD electrode was investigated. No catalytic current could be observed. However, due to the fast cyclic redox reaction of SOD with superoxide, the communication of the protein with the electrode was strongly influenced. The amperometric detection of superoxide radicals is discussed. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:295 / 302
页数:8
相关论文
共 42 条
  • [1] REDOX CHEMISTRY OF SUPEROXIDE-DISMUTASE - CYCLIC VOLTAMMETRY OF WILD-TYPE ENZYMES AND MUTANTS ON FUNCTIONALLY RELEVANT RESIDUES
    AZAB, HA
    BANCI, L
    BORSARI, M
    LUCHINAT, C
    SOLA, M
    VIEZZOLI, MS
    [J]. INORGANIC CHEMISTRY, 1992, 31 (22) : 4649 - 4655
  • [2] POTENTIOMETRIC TITRATIONS AND OXIDATION-REDUCTION POTENTIALS OF SEVERAL IRON SUPEROXIDE DISMUTASES
    BARRETTE, WC
    SAWYER, DT
    FEE, JA
    ASADA, K
    [J]. BIOCHEMISTRY, 1983, 22 (03) : 624 - 627
  • [3] VOLTAMMETRIC BEHAVIOR OF BOVINE ERYTHROCYTE SUPEROXIDE-DISMUTASE
    BORSARI, M
    AZAB, HA
    [J]. BIOELECTROCHEMISTRY AND BIOENERGETICS, 1992, 27 (02): : 229 - 233
  • [4] COBALT BOVINE SUPEROXIDE-DISMUTASE - REACTIVITY OF COBALT CHROMOPHORE IN COPPER-CONTAINING AND IN COPPER-FREE ENZYME
    CALABRESE, L
    COCCO, D
    MORPURGO, L
    MONDOVI, B
    ROTILIO, G
    [J]. EUROPEAN JOURNAL OF BIOCHEMISTRY, 1976, 64 (02): : 465 - 470
  • [5] Copper-zinc superoxide dismutase: Why not pH-dependent?
    Ellerby, LM
    Cabelli, DE
    Graden, JA
    Valentine, JS
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1996, 118 (28) : 6556 - 6561
  • [6] OBSERVATIONS ON OXIDATION-REDUCTION PROPERTIES OF BOVINE ERYTHROCYTE SUPEROXIDE DISMUTASE
    FEE, JA
    DICORLETO, PE
    [J]. BIOCHEMISTRY, 1973, 12 (24) : 4893 - 4899
  • [7] Fridovich I, 1998, J EXP BIOL, V201, P1203
  • [8] BIOLOGY OF OXYGEN RADICALS
    FRIDOVICH, I
    [J]. SCIENCE, 1978, 201 (4359) : 875 - 880
  • [9] GETZOFF ED, 1983, NATURE, V306, P287, DOI 10.1038/306287a0
  • [10] Direct electron transfer between heme-containing enzymes and electrodes as basis for third generation biosensors
    Gorton, L
    Lindgren, A
    Larsson, T
    Munteanu, FD
    Ruzgas, T
    Gazaryan, I
    [J]. ANALYTICA CHIMICA ACTA, 1999, 400 : 91 - 108