Assembly of redox active metallo-enzymes and metallo-peptides on electrodes: Abiological constructs to probe natural processes

Curr Opin Chem Biol. 2022 Jun:68:102142. doi: 10.1016/j.cbpa.2022.102142. Epub 2022 Apr 8.

Abstract

Redox active metallo-proteins and metallo-peptides attached to self-assembled monolayers (SAM) of thiols on Au electrodes or constituting the SAM on Au electrodes can provide unique opportunities to investigate a range of complicated biological phenomena in controlled abiological constructs. In addition to conventional biochemical tools like site-directed mutagenesis, these constructs allow control over electron transfer (ET) processes, micro solvation (SAM design), folding/misfolding and orientation of these biological entities. This article presents a review of the work done by this group in creating abiological bio-inspired SAM on Au electrodes to probe several important biological processes where redox plays or might play a major role. These include stabilisation of different morphologies of Aβ peptides and which allow investigation of the reactivity of their Cu/Zn/heme-bound forms, determination of both outer-sphere and inner-sphere reorganisation energies of cytochrome c along with deciphering the role of the fluxional methionine and finally creation of bio-chemical constructs of cytochrome c oxidase which not only reduce O2 selectively to H2O efficiently but also provide key insights in O2 reduction mechanism which has aided the development of efficient artificial catalysts.

Keywords: Abiological construct; Aβ peptide; Aβ–mediated toxicity; Bio-inspired electrodes; Cytochrome c; Cytochrome c oxidase; Electron transfer; O(2) reduction; Partially reduced oxygen species (PROS); Proton transfer residues; Self-assembled monolayers; Solvent kinetic isotope effect.

Publication types

  • Review
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Electrodes
  • Electron Transport
  • Heme* / metabolism
  • Oxidation-Reduction
  • Peptides*

Substances

  • Peptides
  • Heme