Mechanism of Ca<sup>2+</sup> transport by ferroportin.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 36648329.
- Also identified by DOI 10.7554/eLife.82947 and PMC identifier 9883014.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
Ferroportin (Fpn) is a transporter that releases ferrous ion (Fe<sup>2+</sup>) from cells and is important for homeostasis of iron in circulation. Export of one Fe<sup>2+</sup> by Fpn is coupled to import of two H<sup>+</sup> to maintain charge balance. Here, we show that human Fpn (HsFpn) binds to and mediates Ca<sup>2+</sup> transport. We determine the structure of Ca<sup>2+</sup>-bound HsFpn and identify a single Ca<sup>2+</sup> binding site distinct from the Fe<sup>2+</sup> binding sites. Further studies validate the Ca<sup>2+</sup> binding site and show that Ca<sup>2+</sup> transport is not coupled to transport of another ion. In addition, Ca<sup>2+</sup> transport is significantly inhibited in the presence of Fe<sup>2+</sup> but not vice versa. Function of Fpn as a Ca<sup>2+</sup> uniporter may allow regulation of iron homeostasis by Ca<sup>2+</sup>.
Medical subject headings
- Cation Transport Proteins
- Iron
- Calcium