Determining Redox Potentials of the Iron-Sulfur Clusters of the AdoMet Radical Enzyme Superfamily

被引:8
|
作者
Maiocco, Stephanie J. [1 ]
Walker, Lindsey M. [1 ]
Elliott, Sean J. [1 ]
机构
[1] Boston Univ, Dept Chem, 590 Commonwealth Ave, Boston, MA 02215 USA
来源
RADICAL SAM ENZYMES | 2018年 / 606卷
关键词
METHIONINE LIGAND LABILITY; S-ADENOSYLMETHIONINE; ESCHERICHIA-COLI; DIRECT ELECTROCHEMISTRY; LYSINE 2,3-AMINOMUTASE; REDUCTIVE CLEAVAGE; SAM DEHYDROGENASE; ELECTRON-TRANSFER; BIOTIN SYNTHASE; CYTOCHROMES-C;
D O I
10.1016/bs.mie.2018.06.002
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
While protein film electrochemistry (PFE) has proven to be an effective tool in the interrogation of redox cofactors and assessing the electrocatalytic activity of many different enzymes, recently it has been proven to be useful for the study of the redox potentials of the cofactors of AdoMet radical enzymes (AREs). In this chapter, we review the challenges and opportunities of examining the redox cofactors of AREs in a high level of detail, particularly for the deconvolution of redox potentials of multiple cofactors. We comment on how to best assess the electroactive nature of any given ARE, and we see that when applied well, PFE allows for not only determining redox potentials, but also determining proton-coupling and ligand-binding phenomena in the ARE superfamily.
引用
收藏
页码:319 / 339
页数:21
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