蛋白质工程
脚手架
计算生物学
单克隆抗体
蛋白质设计
免疫原性
支架蛋白
纳米技术
化学
抗体
计算机科学
生物
蛋白质结构
生物化学
材料科学
免疫学
数据库
信号转导
酶
作者
Mohammad Karimi Baba Ahmadi,S A Mohammadi,Manoochehr Makvandi,M. Mamouei,Mohammad Rahmati,Hesam Dehghani,David Wood
出处
期刊:Current Pharmaceutical Biotechnology
[Bentham Science]
日期:2021-06-01
卷期号:22 (7): 878-891
被引量:4
标识
DOI:10.2174/1389201021999200824101035
摘要
In recent years, extensive attention has been given to the generation of new classes of ligand- specific binding proteins to supplement monoclonal antibodies. A combination of protein engineering and display technologies has been used to manipulate non-human antibodies for humanization and stabilization purposes or even the generation of new binding proteins. Engineered protein scaffolds can now be directed against therapeutic targets to treat cancer and immunological disorders. Although very few of these scaffolds have successfully passed clinical trials, their remarkable properties such as robust folding, high solubility, and small size motivate their employment as a tool for biology and applied science studies. Here, we have focused on the generation of new non-Ig binding proteins and single domain antibody manipulation, with a glimpse of their applications.
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