Molecular recognition in copper trafficking

被引:67
作者
Banci, Lucia [1 ,2 ]
Bertini, Ivano [1 ,2 ]
McGreevy, Kathleen S. [1 ,2 ]
Rosato, Antonio [1 ,2 ]
机构
[1] Univ Florence, Magnet Resonance Ctr CERM, I-50019 Sesto Fiorentino, Italy
[2] Univ Florence, Dept Chem, I-50019 Sesto Fiorentino, Italy
关键词
WILSON-DISEASE PROTEIN; CYTOCHROME-C-OXIDASE; N-TERMINAL DOMAIN; METAL-BINDING DOMAINS; X-RAY-ABSORPTION; MENKES-DISEASE; SUPEROXIDE-DISMUTASE; TRANSCRIPTION FACTOR; INTERMEMBRANE SPACE; BACILLUS-SUBTILIS;
D O I
10.1039/b906678k
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
From the basic export of unwanted metal ions in simple organisms to the complex orchestration of metal handling and usage in higher eukaryotes, cellular systems are based on a variety of molecular mechanisms that constrain the right metal to bind to the right protein partner at the right time when needed. A failure to overcome the challenges inherent in this task can lead to pathological states that compromise the life of the cell. This is indeed the case with copper, a metal ion that is essential but which can however also create toxic effects when its intracellular concentration and distribution are not properly controlled. Research in this field increasingly indicates that a subtle interplay between metal coordination chemistry and protein-protein interactions finely tunes molecular recognition.
引用
收藏
页码:695 / 710
页数:16
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