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Iron redox pathway revealed in ferritin via electron transfer analysis

TitleIron redox pathway revealed in ferritin via electron transfer analysis
Publication TypeJournal Article
Year of Publication2020
AuthorsChen P, De Meulenaere E, Deheyn DD, Bandaru PR
Volume10
Pagination4033
Date Published2020/03
ISBN Number2045-2322
Abstract

Ferritin protein is involved in biological tissues in the storage and management of iron - an essential micro-nutrient in the majority of living systems. While there are extensive studies on iron-loaded ferritin, its functionality in iron delivery is not completely clear. Here, for the first time, differential pulse voltammetry (DPV) has been successfully adapted to address the challenge of resolving a cascade of fast and co-occurring redox steps in enzymatic systems such as ferritin. Using DPV, comparative analysis of ferritins from two evolutionary-distant organisms has allowed us to propose a stepwise resolution for the complex mix of concurrent redox steps that is inherent to ferritins and to fine-tune the structure-function relationship of each redox step. Indeed, the cyclic conversion between Fe3+ and Fe2+ as well as the different oxidative steps of the various ferroxidase centers already known in ferritins were successfully discriminated, bringing new evidence that both the 3-fold and 4-fold channels can be functional in ferritin.

DOI10.1038/s41598-020-60640-z
Student Publication: 
No
Research Topics: