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Abstract

In this article, we cross-examine three well-established electrochemical approaches, namely cyclic voltammetry (CV), cyclic square-wave voltammetry (SWV) and electrochemical impedance spectroscopy (EIS) to dissect the electron transfer (ET) rate of electrostatically immobilized cytochrome c on Ag electrodes. A detailed analysis supported by simulations of redox transition provided three distinct values for the heterogeneous electron transfer (HET) rate constant of cyt c interfaced on COOH-terminated C 10 -long alkanethiol, i.e., k HET = 47.8 (±2,91) s -1 in CV, k HET = 64.8 (±1,27) s -1 in SWV, and k HET = 26.5 s -1 in EIS. We discuss the obtained discrepancies obtained from electrochemical methods and compare them with the data from spectro-electrochemical experiments. A comprehensive selection list is created from which the most applicable approach can be chosen for studying proteins of interest. CV is most applicable to study the interfaced proteins exhibiting k HET of ca. 0.5 - 70 s -1 , SWV is suitable for a broader range of k HET of 5 - 120 s -1 and EIS for k HET of 0.5 to 5 s -1 if alkanethiols are used as immobilization strategy.

Keywords

Dielectric spectroscopyCyclic voltammetryElectron transferRedoxAnalytical Chemistry (journal)Electrochemistry

Identifiers

PubMed
37424628
Journal
BBA Advances
Year
2023