Protein Engineering of Redox-Active Enzymes

被引:10
|
作者
Saab-Rincon, Gloria [2 ]
Valderrama, Brenda [1 ]
机构
[1] Univ Nacl Autonoma Mexico, Inst Biotecnol, Dept Med Mol & Bioproc, Cuernavaca 62250, Morelos, Mexico
[2] Univ Nacl Autonoma Mexico, Dept Ingn Celular & Biocatalisis, Cuernavaca 62250, Morelos, Mexico
关键词
SITE-SPECIFIC INCORPORATION; UNNATURAL AMINO-ACIDS; IN-VITRO SELECTION; COLI RIBONUCLEOTIDE REDUCTASE; CYSTEINE-SULFINIC ACID; DE-NOVO DESIGN; ELECTRON-TRANSFER; DIRECTED EVOLUTION; CHEMICAL-SYNTHESIS; CYTOCHROME-C;
D O I
10.1089/ars.2008.2098
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Redox-active enzymes perform many key biological reactions. The electron transfer process is complex, not only because of its versatility, but also because of the intricate and delicate modulation exerted by the protein scaffold on the redox properties of the catalytic sites. Nowadays, there is a wealth of information available about the catalytic mechanisms of redox-active enzymes and the time is propitious for the development of projects based on the protein engineering of redox-active enzymes. In this review, we aim to provide an updated account of the available methods used for protein engineering, including both genetic and chemical tools, which are usually reviewed separately. Specific applications to redox-active enzymes are mentioned within each technology, with emphasis on those cases where the generation of novel functionality was pursued. Finally, we focus on two emerging fields in the protein engineering of redox-active enzymes: the construction of novel nucleic acid-based catalysts and the remodeling of intra-molecular electron transfer networks. We consider that the future development of these areas will represent fine examples of the concurrence of chemical and genetic tools. Antioxid. Redox Signal. 11, 167-192.
引用
收藏
页码:167 / 192
页数:26
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