6W4S

Structure of apo human ferroportin in lipid nanodisc

6W4S の概要

• エントリーDOI: 10.2210/pdb6w4s/pdb
• EMDBエントリー: 21539
• 分子名称: Solute carrier family 40 member 1, Fab45D8 Heavy Chain, Fab45D8 Light Chain (3 entities in total)
• 機能のキーワード: ferroportin, transporter, iron, hepcidin, transport protein-immune system complex, transport protein/immune system
• 由来する生物種: Homo sapiens (Human); 詳細
• タンパク質・核酸の鎖数: 3
• 化学式量合計: 114211.01

構造登録者

Billesboelle, C.B.,Azumaya, C.M.,Gonen, S.,Powers, A.,Kretsch, R.C.,Schneider, S.,Arvedson, T.,Dror, R.O.,Cheng, Y.,Manglik, A. (登録日: 2020-03-11, 公開日: 2020-09-09, 最終更新日: 2024-10-16)

主引用文献

Billesbolle, C.B.,Azumaya, C.M.,Kretsch, R.C.,Powers, A.S.,Gonen, S.,Schneider, S.,Arvedson, T.,Dror, R.O.,Cheng, Y.,Manglik, A.
Structure of hepcidin-bound ferroportin reveals iron homeostatic mechanisms.
Nature, 586:807-811, 2020

PubMed Abstract: The serum level of iron in humans is tightly controlled by the action of the hormone hepcidin on the iron efflux transporter ferroportin. Hepcidin regulates iron absorption and recycling by inducing the internalization and degradation of ferroportin. Aberrant ferroportin activity can lead to diseases of iron overload, such as haemochromatosis, or iron limitation anaemias. Here we determine cryogenic electron microscopy structures of ferroportin in lipid nanodiscs, both in the apo state and in complex with hepcidin and the iron mimetic cobalt. These structures and accompanying molecular dynamics simulations identify two metal-binding sites within the N and C domains of ferroportin. Hepcidin binds ferroportin in an outward-open conformation and completely occludes the iron efflux pathway to inhibit transport. The carboxy terminus of hepcidin directly contacts the divalent metal in the ferroportin C domain. Hepcidin binding to ferroportin is coupled to iron binding, with an 80-fold increase in hepcidin affinity in the presence of iron. These results suggest a model for hepcidin regulation of ferroportin, in which only ferroportin molecules loaded with iron are targeted for degradation. More broadly, our structural and functional insights may enable more targeted manipulation of the hepcidin-ferroportin axis in disorders of iron homeostasis.

PubMed: 32814342
DOI: 10.1038/s41586-020-2668-z

実験手法

ELECTRON MICROSCOPY (3.2 Å)