Mechanisms of iron mineralization in ferritins: one size does not fit all

被引:58
作者
Bradley, Justin M. [1 ]
Moore, Geoffrey R. [1 ]
Le Brun, Nick E. [1 ]
机构
[1] Univ E Anglia, Sch Chem, Ctr Mol & Struct Biochem, Norwich NR4 7TJ, Norfolk, England
来源
JOURNAL OF BIOLOGICAL INORGANIC CHEMISTRY | 2014年 / 19卷 / 06期
基金
英国生物技术与生命科学研究理事会;
关键词
Iron storage; Ferroxidase; Iron metabolism; Dinuclear iron; Mineralization; ESCHERICHIA-COLI BACTERIOFERRITIN; HUMAN H-FERRITIN; CRYSTAL-STRUCTURE; CORE FORMATION; METAL-BINDING; FERROXIDASE REACTION; BACTERIAL FERRITIN; PARALLEL FORMATION; PROTEIN NANOCAGES; STORAGE FUNCTION;
D O I
10.1007/s00775-014-1136-3
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
Significant progress has been made in recent years toward understanding the processes by which an iron mineral is deposited within members of the ferritin family of 24mer iron storage proteins, enabled by high-resolution structures together with spectroscopic and kinetic studies. These suggest common characteristics that are shared between ferritins, namely, a highly symmetric arrangement of subunits that provides a protein coat around a central cavity in which the mineral is formed, channels through the coat that facilitate ingress and egress of ions, and catalytic sites, called ferroxidase centers, that drive Fe2+ oxidation. They also reveal significant variations in both structure and mechanism amongst ferritins. Here, we describe three general types of structurally distinct ferroxidase center and the mechanisms of mineralization that they are associated with. The highlighted variation leads us to conclude that there is no universal mechanism by which ferritins function, but instead there exists several distinct mechanisms of ferritin iron mineralization.
引用
收藏
页码:775 / 785
页数:11
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