Generation and Characterization of SAM Immobilized Enzyme Films in Ionic Liquids

Abstract

Electrochemical investigations of the heme protein dehaloperoxidase (DHP) were undertaken. Motivation for this work lies in the unusual bifunctional nature of DHP, a globin-type protein found in the marine worm Amphitrite ornata. DHP is a monomeric hemoglobin that not only binds and transports dioxygen but features a high level of peroxidase activity for the enzymatic detoxification of halogenated phenolic compounds such as 2,4,6-tribromophenol. Direct electrochemistry of DHP in the absence of mediators was realized for both diffusional and non-diffusional voltammetric cases using mixed OH/COOH self-assembled monolayer modified electrodes of alkanethiolate/gold construction. It appears DHP interacts with anionic electrodes via a lysine patch situated in the vicinity of the heme edge. Interfacial voltammetry suffers from instability problems that have not been completely resolved. Accordingly, mediated thin-layer spectroelectrochemistry was utilized to characterize the Fe(III)/Fe(II) redox thermodynamic properties of DHP. The reduction potential at pH 7 was determined under anaerobic conditions to be +202 mV vs SCE, the most positive value for any known intracellular globin. This unusual value was rationalized in terms of a redox-coupled conformational behavior involving the distal histidine (H55) by analyzing the Gibbs free energy contributions to the potential. The impact of enzyme substrate interactions on redox properties was also characterized and gave evidence for both internal and external binding depending upon the extent of halogen substitution of the phenolic substrate. A cubic thermodynamic cycle was proposed that accounted for both conformational changes and substrate interactions. Finally, several methionine-86 mutants of DHP were prepared to investigate the electron push effect concept for peroxidase activity. The first successful installation of a peroxide-like aspartate-histidine-iron triad into a globin protein was achieved (M86D mutant).

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Document Details

Document Type
Technical Report
Publication Date
Apr 03, 2011
Accession Number
ADA545438

Entities

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  • Edmond F. Bowden
  • Robert A. Mantz

Organizations

  • North Carolina State University

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  • Human Systems

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  • Abstracts
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  • Amino Acids
  • Chemistry
  • Crystal Structure
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  • Electrochemistry
  • Electron Density
  • Electron Transfer
  • Electrons
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  • Histidine
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  • Self Assembled Monolayers
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  • Chemistry

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  • Electrochemical Surface Science
  • Molecular and Cellular Biochemistry
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  • Microelectronics