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  • Title: Affinity binding via zinc(II) for controlled orientation and electrochemistry of histidine-tagged nitrate reductase in self-assembled monolayers.
    Author: Campbell WH, Henig J, Plumeré N.
    Journal: Bioelectrochemistry; 2013 Oct; 93():46-50. PubMed ID: 22894913.
    Abstract:
    Monolayers of Cu(II)-complexes on electrode surfaces are frequently applied for the immobilization and controlled orientation of His-tagged redox proteins. However, affinity binding is limited to applications that require potentials less negative than the reduction potential of the metal complexes. In order to overcome this limitation, we used Zn(2+) cations on nitrilotriacetic acid (NTA) modified carbon electrodes for the coordination of His-tagged nitrate reductase (NaR). The NTA modified electrodes were prepared upon diazotation and electrochemical reduction of an aniline functionalized NTA ligand. After coordination of Zn(2+) to the bound NTA ligand, self-assembly of NaR is achieved via coordination of the imidazole groups from the His-tag to the NTA-Zn(II) complex. The electrochemical investigations of the NaR monolayer on NTA-Zn(II) films demonstrate the catalytic activity for reduction of nitrate to nitrite in the presence of methyl viologen. The catalytic current density correlates with the one expected for a fully active enzyme monolayer. Moreover, the reduction of Zn(2+) is not observed at the potential necessary for the reduction of methyl viologen. Therefore, affinity binding based on Zn(2+) may be used for the immobilization and electrochemical applications of His-tagged NaR.
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