Engineering the Redox Potential over a Wide Range within a New Class of FeS Proteins

被引:47
作者
Zuris, John A. [1 ]
Halim, Danny A. [1 ]
Conlan, Andrea R. [1 ]
Abresch, Edward C. [2 ]
Nechushtai, Rachel [3 ]
Paddock, Mark L. [2 ]
Jennings, Patricia A. [1 ]
机构
[1] Univ Calif San Diego, Dept Chem & Biochem, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Dept Phys, La Jolla, CA 92093 USA
[3] Hebrew Univ Jerusalem, Dept Plant & Environm Sci, Wolfson Ctr Appl Struct Biol, IL-91904 Givat Ram, Israel
关键词
IRON-SULFUR CLUSTERS; 2FE-2S CLUSTER; CRYSTAL-STRUCTURE; MITONEET; HISTIDINE; MUTANT; STATE;
D O I
10.1021/ja103920k
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
MitoNEET is a newly discovered mitochondrial protein and a target of the TZD class of antidiabetes drugs. MitoNEET is homodimeric with each protomer binding a [2Fe-2S] center through a rare 3-Cys and 1-His coordination geometry. Both the fold and the coordination of the [2Fe-2S] centers suggest that it could have novel properties compared to other known [2Fe-2S] proteins. We tested the robustness of mitoNEET to mutation and the range over which the redox potential (E-M) could be tuned. We found that the protein could tolerate an array of mutations that modified the E-M of the [2Fe-2S] center over a range of similar to 700 mV, which is the largest E-M range engineered in an FeS protein and, importantly, spans the cellular redox range (+200 to -300 mV). These properties make mitoNEET potentially useful for both physiological studies and industrial applications as a stable, water-soluble, redox agent.
引用
收藏
页码:13120 / 13122
页数:3
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