Impaired iron transport activity of ferroportin 1 in hereditary iron overload

J Membr Biol. 2005 Jul;206(1):3-7. doi: 10.1007/s00232-005-0768-1.

Abstract

To investigate the functional significance of mutations in Ferroportin that cause hereditary iron overload, we directly measured the iron efflux activity of the proteins expressed in Xenopus oocytes. We found that wild type and mutant Ferroportin molecules (A77D, N144H, Q248H and V162Delta) were all expressed at the plasma membrane at similar levels. All mutations caused significant reductions in (59)Fe efflux compared to wild type but all retained some residual transport activity. A77D had the strongest effect on (59)Fe efflux (remaining activity 9% of wild-type control), whereas the N144H mutation retained the highest efflux activity (42% of control). The Q248H and V162Delta mutations were intermediate between these values. Co-injection of mutant and wild-type mRNAs revealed that the A77D and N144H mutations had a dominant negative effect on the function of the WT protein.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biological Transport, Active
  • Cation Transport Proteins / genetics*
  • Cation Transport Proteins / metabolism*
  • Cells, Cultured
  • Hemochromatosis / genetics*
  • Hemochromatosis / metabolism*
  • Humans
  • Iron / metabolism*
  • Mutagenesis, Site-Directed
  • Oocytes / metabolism*
  • Structure-Activity Relationship
  • Xenopus laevis

Substances

  • Cation Transport Proteins
  • metal transporting protein 1
  • Iron