Determining Redox Potentials of the Iron-Sulfur Clusters of the AdoMet Radical Enzyme Superfamily

Methods Enzymol. 2018:606:319-339. doi: 10.1016/bs.mie.2018.06.002. Epub 2018 Jul 5.

Abstract

While protein film electrochemistry (PFE) has proven to be an effective tool in the interrogation of redox cofactors and assessing the electrocatalytic activity of many different enzymes, recently it has been proven to be useful for the study of the redox potentials of the cofactors of AdoMet radical enzymes (AREs). In this chapter, we review the challenges and opportunities of examining the redox cofactors of AREs in a high level of detail, particularly for the deconvolution of redox potentials of multiple cofactors. We comment on how to best assess the electroactive nature of any given ARE, and we see that when applied well, PFE allows for not only determining redox potentials, but also determining proton-coupling and ligand-binding phenomena in the ARE superfamily.

Keywords: Electrochemistry; Iron–sulfur cluster; Protein film electrochemistry; Voltammetry.

Publication types

  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • Coenzymes / chemistry
  • Coenzymes / metabolism*
  • Electrochemistry
  • Enzyme Assays / methods*
  • Enzymes / metabolism*
  • Free Radicals / metabolism
  • Ligands
  • Models, Molecular
  • Oxidation-Reduction
  • Protein Binding
  • S-Adenosylmethionine / metabolism*

Substances

  • Coenzymes
  • Enzymes
  • Free Radicals
  • Ligands
  • S-Adenosylmethionine