连接器
蛋白质工程
共价键
纳米技术
融合蛋白
领域(数学分析)
万花筒
小分子
功能(生物学)
计算机科学
组合化学
化学
酶
计算生物学
材料科学
重组DNA
生物化学
生物
细胞生物学
有机化学
数学分析
数学
程序设计语言
基因
操作系统
作者
Shengwang Zhou,Yuan Wei
标识
DOI:10.1016/j.biotechadv.2023.108147
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 between 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.
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