| Literature DB >> 33190422 |
Chandrika N Deshpande1, Corbin R Azucenas2,3, Bo Qiao4, Norimichi Nomura5, Vicky Xin1, Josep Font1, So Iwata5, Tomas Ganz4,6, Elizabeta Nemeth4, Bryan Mackenzie3,4, Mika Jormakka1.
Abstract
Ferroportin (Fpn) is an essential mammalian iron transporter that is negatively regulated by the hormone hepcidin. Our current molecular understanding of Fpn-mediated iron efflux and regulation is limited due to a lack of biochemical, biophysical and high-resolution structural studies. A critical step towards understanding the transport mechanism of Fpn is to obtain sufficient quantities of pure and stable protein for downstream studies. As such, we detail here an expression and purification protocol for mouse Fpn yielding milligram quantities of pure protein. We have generated deletion constructs exhibiting enhanced thermal stability and which retained iron-transport activity and hepcidin responsiveness, providing a platform for further biophysical studies of Fpn.Entities:
Keywords: ferroportin; hepcidin regulation; iron metabolism; thermostabilization
Mesh:
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Year: 2020 PMID: 33190422 PMCID: PMC7780100 DOI: 10.1002/2211-5463.13039
Source DB: PubMed Journal: FEBS Open Bio ISSN: 2211-5463 Impact factor: 2.792