Dynamic Copper(I) Imaging in Mammalian Cells with a Genetically Encoded Fluorescent Copper(I) Sensor

被引:124
作者
Wegner, Seraphine V.
Arslan, Hasan
Sunbul, Murat
Yin, Jun
He, Chuan [1 ]
机构
[1] Univ Chicago, Dept Chem, Chicago, IL 60637 USA
基金
美国国家科学基金会;
关键词
THIOLATE POLYNUCLEAR CLUSTER; TRANSCRIPTION FACTOR; LIVING CELLS; SACCHAROMYCES-CEREVISIAE; SUPEROXIDE-DISMUTASE; CANDIDA-GLABRATA; AQUEOUS-SOLUTION; RAT HEPATOCYTES; PROTEINS; DOMAIN;
D O I
10.1021/ja9097324
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Copper, a key cofactor for many life processes, is toxic at elevated levels, and its availability is strictly controlled inside cells. Therefore, it is a challenge to Visualize copper availability in the tight copper-binding environment of the cell. We report a genetically encoded fluorescent copper(I) sensor based on the copper(I)-binding-induced conformational change of a copper-responsive transcriptional regulator, Amt 1. The resulting reporter, Amt1-FRET, is ratiometric, highly sensitive (K-d = 2.5 x 10(-18) M), and selective toward copper(I). Its measured high affinity to copper(I) confirms the extremely low copper availability in yeast since Amt1 senses the upper limit of cellular copper levels in yeast and activates copper detoxification genes. Amt1-FRET operates in the dynamic range of the cellular copper buffer in mammalian cells and can report dynamic fluctuations of the cellular copper availability within minutes of perturbation. Thus, Amt1-FRET visualizes the tightly controlled copper availability in mammalian cells.
引用
收藏
页码:2567 / +
页数:4
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