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
相关论文
共 26 条
[1]   Redox Characterization of the FeS Protein MitoNEET and Impact of Thiazolidinedione Drug Binding [J].
Bak, Daniel W. ;
Zuris, John A. ;
Paddock, Mark L. ;
Jennings, Patricia A. ;
Elliott, Sean J. .
BIOCHEMISTRY, 2009, 48 (43) :10193-10195
[2]   Iron-sulfur clusters: Nature's modular, multipurpose structures [J].
Beinert, H ;
Holm, RH ;
Munck, E .
SCIENCE, 1997, 277 (5326) :653-659
[3]   Crystal structures of ferredoxin variants exhibiting large changes in [Fe-S] reduction potential [J].
Chen, KS ;
Bonagura, CA ;
Tilley, GJ ;
McEvoy, JP ;
Jung, YS ;
Armstrong, FA ;
Stout, CD ;
Burgess, BK .
NATURE STRUCTURAL BIOLOGY, 2002, 9 (03) :188-192
[4]   Identification of a novel mitochondrial protein ("mitoNEET") cross-linked specifically by a thiazolidinedione photoprobe [J].
Colca, JR ;
McDonald, WG ;
Waldon, DJ ;
Leone, JW ;
Lull, JM ;
Bannow, CA ;
Lund, ET ;
Mathews, WR .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2004, 286 (02) :E252-E260
[5]   Crystal Structure of Miner1: The Redox-active 2Fe-2S Protein Causative in Wolfram Syndrome 2 [J].
Conlan, Andrea R. ;
Axelrod, Herbert L. ;
Cohen, Aina E. ;
Abresch, Edward C. ;
Zuris, John ;
Yee, David ;
Nechushtai, Rachel ;
Jennings, Patricia A. ;
Paddock, Mark L. .
JOURNAL OF MOLECULAR BIOLOGY, 2009, 392 (01) :143-153
[6]   Structural Comparison Of A Diabetes Drug Target, Mitoneet, A 2Fe-2S Cluster Protein To Its More Stable Mutant, H87C [J].
Conlan, Andrea R. ;
Axelrod, Herbert L. ;
Cohen, Aina E. ;
Abresch, Edward C. ;
Nechushtai, Rachel ;
Paddock, Mark L. ;
Jennings, Patricia A. .
BIOPHYSICAL JOURNAL, 2009, 96 (03) :67A-67A
[7]   Alteration of the midpoint potential and catalytic activity of the Rieske iron-sulfur protein by changes of amino acids forming hydrogen bonds to the iron-sulfur cluster [J].
Denke, E ;
Merbitz-Zahradnik, T ;
Hatzfeld, OM ;
Snyder, CH ;
Link, TA ;
Trumpower, BL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (15) :9085-9093
[8]   Binding of Histidine in the (Cys)3(His)1-Coordinated [2Fe-2S] Cluster of Human mitoNEET [J].
Dicus, Michelle M. ;
Conlan, Andrea ;
Nechushtai, Rachel ;
Jennings, Patricia A. ;
Paddock, Mark L. ;
Britt, R. David ;
Stoll, Stefan .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2010, 132 (06) :2037-2049
[9]  
Dutton P L, 1978, Methods Enzymol, V54, P411
[10]   Iron-sulfur clusters: ever-expanding roles [J].
Fontecave, M .
NATURE CHEMICAL BIOLOGY, 2006, 2 (04) :171-174