Rational Design of Artificial Metalloenzymes: Case Studies in Myoglobin

被引:1
|
作者
Lin, Yingwu [1 ,2 ]
机构
[1] Univ South China, Sch Chem & Chem Engn, Hengyang 421001, Peoples R China
[2] Univ South China, Lab Prot Struct & Funct, Hengyang 421001, Peoples R China
基金
中国国家自然科学基金;
关键词
metalloprotein; metalloenzyme; heme protein; myoglobin; molecular design; NITRITE REDUCTASE-ACTIVITY; UNNATURAL AMINO-ACIDS; HEME-COPPER OXIDASE; DISULFIDE BOND; STRUCTURAL BASIS; CROSS-LINK; GENETIC INCORPORATION; DISTAL HISTIDINES; OXYGEN ACTIVATION; PROTEIN SCAFFOLD;
D O I
10.7536/PC180528
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Metalloenzymes play diverse important functions in biological systems. Meanwhile, design of artificial metalloenzymes may fine-tune and expand the functionalities of natural metalloenzymes, and even create novel enzymes with more advanced functions. Myoglobin (Mb) is an ideal protein model for design of heme proteins and other metalloenzymes. In recent years, various approaches have been developed for design of artificial metalloenzymes based on the protein scaffold of Mb, which include design of hydrogen-bonding network, intramolecular disulfide bond, the use of post-translational modifications, introduction of non-natural amino acids and non-native cofactors. This review summaries the recent progress in these aspects, which will help us understand the structure and function relationship of metalloenzymes, master the idea and methodologies of artificial metalloenzyme design, thereby promoting the rapid development in this field.
引用
收藏
页码:1464 / 1474
页数:11
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