Diversity of structures and functions of oxo-bridged non-heme diiron proteins

Arch Biochem Biophys. 2021 Jul 15:705:108917. doi: 10.1016/j.abb.2021.108917. Epub 2021 May 12.

Abstract

Oxo-bridged diiron proteins are a distinct class of non-heme iron proteins. Their active sites are composed of two irons that are coordinated by amino acid side chains, and a bridging oxygen that interacts with each iron. These proteins are members of the ferritin superfamily and share the structural feature of a four α-helix bundle that provides the residues that coordinate the irons. The different proteins also display a wide range of structures and functions. A prototype of this family is hemerythrin, which functions as an oxygen transporter. Several other hemerythrin-like proteins have been described with a diversity of functions including oxygen and iron sensing, and catalytic activities. Rubrerythrins react with hydrogen peroxide and rubrerythrin-like proteins possess a rubredoxin domain, in addition to the oxo-bridged diiron center. Other redox enzymes with oxo-bridged irons include flavodiiron proteins that act as O2 or NO reductases, ribonucleotide reductase and methane monooxygenase. Ferritins have an oxo-bridged diiron in the ferroxidase center of the protein, which plays a role in the iron storage function of these proteins. There are also bacterial ferritins that exhibit catalytic activities. The structures and functions of this broad class of oxo-bridged diiron proteins are described and compared in this review.

Keywords: Ferritin; Flavodiiron protein; Hemerythrin; Methane monooxygenase; Ribonucleotide reductase; Rubrerythrin.

Publication types

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

MeSH terms

  • Animals
  • Ferritins / chemistry
  • Ferritins / metabolism
  • Hemerythrin / chemistry
  • Hemerythrin / metabolism
  • Humans
  • Iron* / chemistry
  • Iron* / metabolism
  • Nonheme Iron Proteins / chemistry
  • Nonheme Iron Proteins / metabolism
  • Oxidation-Reduction
  • Oxygen* / chemistry
  • Oxygen* / metabolism

Substances

  • Iron
  • Oxygen
  • Nonheme Iron Proteins
  • Hemerythrin
  • Ferritins