The Ferroxidase-Permease System for Transport of Iron Across Membranes: From Yeast to Humans

被引:1
作者
Amadei, Matteo [1 ]
Polticelli, Fabio [2 ]
Musci, Giovanni [3 ]
di Patti, Maria Carmela Bonaccorsi [1 ]
机构
[1] Sapienza Univ Rome, Dept Biochem Sci A Rossi Fanelli, I-00185 Rome, Italy
[2] Univ Roma Tre, Dept Sci, I-00146 Rome, Italy
[3] Univ Molise, Dept Biosci & Terr, I-86090 Pesche, Italy
关键词
ferroxidase; multicopper oxidase; ceruloplasmin; hephaestin; ferroportin; Fet3; Ftr1; yeast; iron; copper; MULTICOPPER OXIDASE FET3P; GLYCOSYLPHOSPHATIDYLINOSITOL-ANCHORED CERULOPLASMIN; SACCHAROMYCES-CEREVISIAE; COPPER INCORPORATION; CANDIDA-ALBICANS; FUNCTIONAL-CHARACTERIZATION; MOLECULAR-MECHANISM; HUMAN FERROPORTIN; STRUCTURAL MODEL; PICHIA-PASTORIS;
D O I
10.3390/ijms26030875
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Transport of iron across the cell membrane is a tightly controlled process carried out by specific proteins in all living cells. In yeast and in mammals, a system formed by an enzyme with ferroxidase activity coupled to a membrane transporter supports iron uptake or iron efflux, respectively. Ferroxidase belongs to the family of blue multicopper oxidases, enzymes able to couple the one-electron oxidation of substrate(s) to full reduction of molecular oxygen to water. On the other hand, the permeases are widely different and are specific to Fe3+ and Fe2+ in yeast and multicellular organisms, respectively. This review will describe the yeast and human ferroxidase-permease systems, highlighting similarities and differences in structure, function and regulation of the respective protein components.
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共 147 条
[131]   Functional analysis and theoretical modeling of ferroportin reveals clustering of mutations according to phenotype [J].
Wallace, Daniel F. ;
Harris, Jonathan M. ;
Subramaniam, V. Nathan .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2010, 298 (01) :C75-C84
[132]   Involvement of chloride channels in hepatic copper metabolism: CIC-4 promotes copper incorporation into ceruloplasmin [J].
Wang, T ;
Weinman, SA .
GASTROENTEROLOGY, 2004, 126 (04) :1157-1166
[133]   Targeted suppression of the ferroxidase and iron trafficking activities of the multicopper oxidase Fet3p from Saccharomyces cerevisiae [J].
Wang, TP ;
Quintanar, L ;
Severance, S ;
Solomon, EI ;
Kosman, DJ .
JOURNAL OF BIOLOGICAL INORGANIC CHEMISTRY, 2003, 8 (06) :611-620
[134]   Structural basis of ferroportin inhibition by minihepcidin PR73 [J].
Wilbon, Azaan Saalim ;
Shen, Jiemin ;
Ruchala, Piotr ;
Zhou, Ming ;
Pan, Yaping .
PLOS BIOLOGY, 2023, 21 (01)
[135]   Toxicity of iron and hydrogen peroxide: The Fenton reaction [J].
Winterbourn, CC .
TOXICOLOGY LETTERS, 1995, 82-3 :969-974
[136]   A comparison of ceruloplasmin to biological polyanions in promoting the oxidation of Fe2+ under physiologically relevant conditions [J].
Wong, Bruce X. ;
Ayton, Scott ;
Lam, Linh Q. ;
Lei, Peng ;
Adlard, Paul A. ;
Bush, Ashley I. ;
Duce, James A. .
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS, 2014, 1840 (12) :3299-3310
[137]   Iron-regulated DNA binding by the AFT1 protein controls the iron regulon in yeast [J].
YamaguchiIwai, Y ;
Stearman, R ;
Dancis, A ;
Klausner, RD .
EMBO JOURNAL, 1996, 15 (13) :3377-3384
[139]   The new role of poly (rC)-binding proteins as iron transport chaperones: Proteins that could couple with inter-organelle interactions to safely traffic iron [J].
Yanatori, Izumi ;
Richardson, Des R. ;
Toyokuni, Shinya ;
Kishi, Fumio .
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS, 2020, 1864 (11)
[140]   Iron Export through the Transporter Ferroportin 1 Is Modulated by the Iron Chaperone PCBP2 [J].
Yanatori, Izumi ;
Richardson, Des R. ;
Imada, Kiyoshi ;
Kishi, Fumio .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2016, 291 (33) :17303-17318