Kaleidoscope megamolecules synthesis and application using self-assembly technology

被引:4
|
作者
Zhou, Shengwang [1 ]
Wei, Yuan [1 ]
机构
[1] Jiangsu Univ, Sch Pharm, Zhenjiang 212013, Peoples R China
基金
中国国家自然科学基金;
关键词
Protein engineering; Megamolecule; Recombinant functional protein; Self; -assembly; Antibody mimic; ENZYME; PROTEINS; BINDING; DESIGN; PURIFICATION; PEGYLATION; EXPRESSION; CUTINASE; LINKERS; CELLS;
D O I
10.1016/j.biotechadv.2023.108147
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
The megamolecules with high ordered structures play an important role in chemical biology and biomedical engineering. Self-assembly, a long-discovered but very appealing technique, could induce many reactions be-tween biomacromolecules and organic linking molecules, such as an enzyme domain and its covalent inhibitors. Enzyme and its small-molecule inhibitors have achieved many successes in medical application, which realize the catalysis process and theranostic function. By employing the protein engineering technology, the building blocks of enzyme fusion protein and small molecule linker can be assembled into a novel architecture with the specified organization and conformation. Molecular level recognition of enzyme domain could provide both covalent reaction sites and structural skeleton for the functional fusion protein. In this review, we will discuss the range of tools available to combine functional domains by using the recombinant protein technology, which can assemble them into precisely specified architectures/valences and develop the kaleidoscope megamolecules for catalytic and medical application.
引用
收藏
页数:10
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