Mechanism of ferrous iron binding and oxidation by ferritin from a pennate diatom

Pfaffen, Stephanie, Abdulqadir, Raz, Le Brun, Nick E and Murphy, Michael E P (2013) Mechanism of ferrous iron binding and oxidation by ferritin from a pennate diatom. The Journal of Biological Chemistry, 288 (21). pp. 14917-14925. ISSN 1083-351X

Full text not available from this repository. (Request a copy)

Abstract

A novel ferritin was recently found in Pseudo-nitzschia multiseries (PmFTN), a marine pennate diatom that plays a major role in global primary production and carbon sequestration into the deep ocean. Crystals of recombinant PmFTN were soaked in iron and zinc solutions, and the structures were solved to 1.65-2.2-Å resolution. Three distinct iron binding sites were identified as determined from anomalous dispersion data from aerobically grown ferrous soaked crystals. Sites A and B comprise the conserved ferroxidase active site, and site C forms a pathway leading toward the central cavity where iron storage occurs. In contrast, crystal structures derived from anaerobically grown and ferrous soaked crystals revealed only one ferrous iron in the active site occupying site A. In the presence of dioxygen, zinc is observed bound to all three sites. Iron oxidation experiments using stopped-flow absorbance spectroscopy revealed an extremely rapid phase corresponding to Fe(II) oxidation at the ferroxidase site, which is saturated after adding 48 ferrous iron to apo-PmFTN (two ferrous iron per subunit), and a much slower phase due to iron core formation. These results suggest an ordered stepwise binding of ferrous iron and dioxygen to the ferroxidase site in preparation for catalysis and a partial mobilization of iron from the site following oxidation.

Item Type: Article
Uncontrolled Keywords: binding sites,crystallography, x-ray,diatoms,ferritins,iron,oxidation-reduction,protein binding,protein structure, tertiary,recombinant proteins
Faculty \ School: Faculty of Science > School of Chemistry
Depositing User: Pure Connector
Date Deposited: 09 Jul 2014 10:10
Last Modified: 17 Sep 2020 23:55
URI: https://ueaeprints.uea.ac.uk/id/eprint/49065
DOI: 10.1074/jbc.M113.454496

Actions (login required)

View Item View Item