Metal trafficking: from maintaining the metal homeostasis to future drug design

被引:81
作者
Ba, Lalla Aicha [1 ]
Doering, Mandy [1 ]
Burkholz, Torsten [1 ]
Jacob, Claus [1 ]
机构
[1] Univ Saarland, Sch Pharm, Div Bioorgan Chem, D-66123 Saarbrucken, Germany
关键词
MOLYBDENUM COFACTOR; IRON CHELATORS; IN-VITRO; PHOTODYNAMIC THERAPY; CARBONIC-ANHYDRASE; HYDROGEN-PEROXIDE; ACTIVE-SITE; CHLAMYDOMONAS-REINHARDTII; XANTHINE DEHYDROGENASE; MOLECULAR-MECHANISMS;
D O I
10.1039/b904533c
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
The diverse proteins and enzymes involved in metal trafficking between and inside human cells form numerous transport networks which Lire highly specific for each essential metal ion and apoprotein. Individual players include voltage-gated ion channels, import and export proteins, intracellular metal-ion sensors, storage proteins and chaperones. In the case of calcium, iron and copper, some of the most apparent trafficking avenues are now well established in eukaryotes, while others are just emerging (e.g. for zinc, manganese and molybdenum). Chemistry provides an important contribution to many issues surrounding these transport pathways, from metal binding-constants and ion specificity to metal-ion exchange kinetics. Ultimately, a better Understanding of these processes opens up opportunities for metal-ion-related therapy, which goes beyond traditional chelate-based metal ion detoxification.
引用
收藏
页码:292 / 311
页数:20
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