Arginine deiminase: recent advances in discovery, crystal structure, and protein engineering for improved properties as an anti-tumor drug

被引:31
作者
Han, Rui-Zhi [1 ,2 ]
Xu, Guo-Chao [1 ,2 ]
Dong, Jin-Jun [1 ,2 ]
Ni, Ye [1 ,2 ]
机构
[1] Jiangnan Univ, Sch Biotechnol, Minist Educ, Key Lab Carbohydrate Chem & Biotechnol, Wuxi 214122, Peoples R China
[2] Jiangnan Univ, Sch Biotechnol, Minist Educ, Key Lab Ind Biotechnol, Wuxi 214122, Peoples R China
基金
中国国家自然科学基金;
关键词
Arginine deiminase (ADI); Protein engineering; Directed evolution; PEGylation; Anti-tumor; PSEUDOMONAS-PLECOGLOSSICIDA CGMCC2039; ADI-PEG; 20; ARGININOSUCCINATE SYNTHETASE; STREPTOCOCCUS-PYOGENES; ESCHERICHIA-COLI; PROMOTER METHYLATION; DIRECTED EVOLUTION; SIGNAL PEPTIDE; IN-VITRO; DEPRIVATION;
D O I
10.1007/s00253-016-7490-z
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Arginine deiminase (ADI) is an important arginine-degrading enzyme with wide applications, in particular as an anti-cancer agent for the therapy of arginine-auxotrophic tumors. In recent years, novel ADIs with excellent properties have been identified from various organisms, and crystal structures of ADI were investigated. To satisfy the requirements of potential therapeutic applications, protein engineering has been performed to improve the activity and properties of ADIs. In this mini-review, we systematically summarized the latest progress on identification and crystal structure of ADIs, and protein engineering strategies for improved enzymatic properties, such as pH optimum, K (m) and k (cat) values, and thermostability. We also outlined the PEGylation of ADI for improved circulating half-life and immunogenicity, as well as their performance in clinical trials. Finally, perspectives on extracellular secretion and property improvement of ADI were discussed.
引用
收藏
页码:4747 / 4760
页数:14
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