Site-Specific Selenocysteine Incorporation into Proteins by Genetic Engineering

被引:7
作者
Wang, Yuchuan [1 ,3 ]
Liu, Pengcheng [2 ]
Chang, Jiao [2 ]
Xu, Yunping [1 ]
Wang, Jiangyun [1 ,2 ,3 ]
机构
[1] Shenzhen Inst Transfus Med, Shenzhen Blood Ctr, Shenzhen 518052, Peoples R China
[2] Chinese Acad Sci, Inst Biophys, Beijing 100101, Peoples R China
[3] Chinese Acad Sci, Shenzhen Inst Adv Technol, Inst Synthet Biol, 1068 Xueyuan Ave, Shenzhen, Peoples R China
基金
国家重点研发计划;
关键词
selenocysteine; genetic engineering; selenoprotein; ELONGATION-FACTOR TU; CONTAINING CATALYTIC ANTIBODY; ESCHERICHIA-COLI; TRANSFER-RNA; GLUTATHIONE-PEROXIDASE; SELENIUM; SELENOPROTEINS; EXPRESSION; TRNA(SEC); INSERTION;
D O I
10.1002/cbic.202100124
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
Selenocysteine (Sec), a rare naturally proteinogenic amino acid, is the major form of essential trace element selenium in living organisms. Selenoproteins, with one or several Sec residues, are found in all three domains of life. Many selenoproteins play a role in critical cellular functions such as maintaining cell redox homeostasis. Sec is usually encoded by an in-frame stop codon UGA in the selenoprotein mRNA, and its incorporation in vivo is highly species-dependent and requires the reprogramming of translation. This mechanistic complexity of selenoprotein synthesis poses a big challenge to produce synthetic selenoproteins. To understand the functions of natural as well as engineered selenoproteins, many strategies have recently been developed to overcome the inherent barrier for recombinant selenoprotein production. In this review, we will describe the progress in selenoprotein production methodology.
引用
收藏
页码:2918 / 2924
页数:7
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