Electrochemical characterization of dehaloperoxidase adsorbates on COOH/OH mixed self-assembled monolayers

被引:6
作者
Chen, Thomas K. [1 ]
Bowden, Edmond F. [1 ]
机构
[1] N Carolina State Univ, Dept Chem, Raleigh, NC 27695 USA
关键词
Dehaloperoxidase; Protein adsorption; Globin electrochemistry; Diffusionless voltammetry; Self-assembled monolayers; DIRECT ELECTRON-TRANSFER; CYTOCHROME-C; DYNAMIC DOCKING; ADSORPTIVE IMMOBILIZATION; PROTEIN; MYOGLOBIN; SURFACE; ORIENTATION; B(5); HEMOGLOBIN;
D O I
10.1016/j.jelechem.2013.05.023
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Electrochemical characterization of Amphitrite ornata dehaloperoxidase, a monomeric hemoglobin, adsorbed on COOH/OH-terminated alkanethiolate mixed self-assembled monolayers (SAMs) is reported. Adsorption was achieved by simple electrode exposure to low ionic strength protein solution at pH 6.0, and cyclic voltammetry (CV) was employed to measure surface concentration, electron transfer rate, and formal potential under anaerobic conditions. Surface concentration values determined by CV were found to be inversely proportional to scan rate, a behavior that is different than that observed for electron transfer proteins such as cytochrome c. We attribute this behavior to a dynamic heterogeneous adsorbate layer that permits some fraction of the molecules to undergo reorientation during a CV scan. A model was proposed that classifies adsorbates among three populations with respect to their most stable orientations, namely, electroactive adsorbates, latent electroinactive adsorbates capable of undergoing reorientation to electroactive states, and electroinactive adsorbates. Electrochemical results and the proposed model are discussed in terms of the tertiary structure and surface properties of dehaloperoxidase and are compared to the docking and electron transfer reactions of the myoglobin/cytochrome b(5) system. Examination of the effects of ionic strength and mixed SAM composition provide support for the proposed model. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:23 / 28
页数:6
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