The relationship between redox enzyme activity and electrochemical potential-cellular and mechanistic implications from protein film electrochemistry

被引:24
作者
Gates, Andrew J.
Kemp, Gemma L.
To, Chun Yip
Mann, James
Marritt, Sophie J.
Mayes, Andrew G.
Richardson, David J.
Butt, Julea N. [1 ]
机构
[1] Univ E Anglia, Ctr Mol & Struct Biochem, Sch Chem, Norwich NR4 7TJ, Norfolk, England
基金
英国生物技术与生命科学研究理事会;
关键词
PERIPLASMIC NITRATE REDUCTASE; C NITRITE REDUCTASE; CATALYTIC ELECTRON-TRANSPORT; REORGANIZATION FREE-ENERGIES; 4-HELIX BUNDLE PROTEIN; ESCHERICHIA-COLI; PARACOCCUS-PANTOTROPHUS; CYTOCHROME-C; DMSO REDUCTASE; SUCCINATE-DEHYDROGENASE;
D O I
10.1039/c0cp02887h
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In protein film electrochemistry a redox protein of interest is studied as an electroactive film adsorbed on an electrode surface. For redox enzymes this configuration allows quantification of the relationship between catalytic activity and electrochemical potential. Considered as a function of enzyme environment, i.e., pH, substrate concentration etc., the activity-potential relationship provides a fingerprint of activity unique to a given enzyme. Here we consider the nature of the activity-potential relationship in terms of both its cellular impact and its origin in the structure and catalytic mechanism of the enzyme. We propose that the activity-potential relationship of a redox enzyme is tuned to facilitate cellular function and highlight opportunities to test this hypothesis through computational, structural, biochemical and cellular studies.
引用
收藏
页码:7720 / 7731
页数:12
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