Human ferroportin mediates proton-coupled active transport of iron
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作者:
Li, Shuang
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Washington Univ, Dept Biochem & Mol Biophys, Sch Med, 660 S Euclid Ave, St Louis, MO 63110 USAWashington Univ, Dept Biochem & Mol Biophys, Sch Med, 660 S Euclid Ave, St Louis, MO 63110 USA
Li, Shuang
[1
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Yang, Yihu
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Washington Univ, Dept Biochem & Mol Biophys, Sch Med, 660 S Euclid Ave, St Louis, MO 63110 USAWashington Univ, Dept Biochem & Mol Biophys, Sch Med, 660 S Euclid Ave, St Louis, MO 63110 USA
Yang, Yihu
[1
]
Li, Weikai
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Washington Univ, Dept Biochem & Mol Biophys, Sch Med, 660 S Euclid Ave, St Louis, MO 63110 USAWashington Univ, Dept Biochem & Mol Biophys, Sch Med, 660 S Euclid Ave, St Louis, MO 63110 USA
Li, Weikai
[1
]
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[1] Washington Univ, Dept Biochem & Mol Biophys, Sch Med, 660 S Euclid Ave, St Louis, MO 63110 USA
As the sole iron exporter in humans, ferroportin controls systemic iron homeostasis through exporting iron into the blood plasma. The molecular mechanism of how ferroportin exports iron under various physiological settings remains unclear. Here we found that purified ferroportin incorporated into liposomes preferentially transports Fe2+ and exhibits lower affinities of transporting other divalent metal ions. The iron transport by ferroportin is facilitated by downhill proton gradients at the same direction. Human ferroportin is also capable of transporting protons, and this activity is tightly coupled to the iron transport. Remarkably, ferroportin can conduct active transport uphill against the iron gradient, with favorable charge potential providing the driving force. Targeted mutagenesis suggests that the iron translocation site is located at the pore region of human ferroportin. Together, our studies enhance the mechanistic understanding by which human ferroportin transports iron and suggest that a combination of electrochemical gradients regulates iron export.
机构:
Newcastle Univ, Fac Med Sci, Epithelial Res Grp, Inst Cell & Mol Biosci, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, EnglandNewcastle Univ, Fac Med Sci, Epithelial Res Grp, Inst Cell & Mol Biosci, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England
Anderson, Catriona M. H.
Thwaites, David T.
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Newcastle Univ, Fac Med Sci, Epithelial Res Grp, Inst Cell & Mol Biosci, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, EnglandNewcastle Univ, Fac Med Sci, Epithelial Res Grp, Inst Cell & Mol Biosci, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England
机构:
NYU, Dept Chem, New York, NY 10012 USANYU, Dept Chem, New York, NY 10012 USA
Li, Jianping
Li, Yan
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NYU, Sch Med, Dept Cell Biol, New York, NY 10012 USANYU, Dept Chem, New York, NY 10012 USA
Li, Yan
Koide, Akiko
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机构:
NYU, Perlmutter Canc Ctr, Sch Med, New York, NY USA
NYU, Sch Med, Dept Med, New York, NY USANYU, Dept Chem, New York, NY 10012 USA
Koide, Akiko
Kuang, Huihui
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New York Struct Biol Ctr, Simons Electron Microscopy Ctr, New York, NY USANYU, Dept Chem, New York, NY 10012 USA
Kuang, Huihui
Torres, Victor J.
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NYU, Sch Med, Dept Microbiol, New York, NY USA
NYU, Sch Med, Antimicrobial Resistant Pathogens Program, New York, NY USANYU, Dept Chem, New York, NY 10012 USA
Torres, Victor J.
Koide, Shohei
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NYU, Perlmutter Canc Ctr, Sch Med, New York, NY USA
NYU, Sch Med, Dept Biochem & Mol Pharmacol, New York, NY USANYU, Dept Chem, New York, NY 10012 USA
Koide, Shohei
Wang, Da-Neng
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NYU, Sch Med, Dept Cell Biol, New York, NY 10012 USANYU, Dept Chem, New York, NY 10012 USA
Wang, Da-Neng
Traaseth, Nathaniel J.
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NYU, Dept Chem, New York, NY 10012 USANYU, Dept Chem, New York, NY 10012 USA
机构:
Albert Einstein Coll Med, Dept Physiol & Biophys, Bronx, NY 10461 USA
Albert Einstein Coll Med, Dept Neurosci, Bronx, NY 10461 USAAlbert Einstein Coll Med, Dept Physiol & Biophys, Bronx, NY 10461 USA