Mirror-image protein and peptide drug discovery through mirror-image phage display

被引:21
|
作者
Qi, Yun-Kun [1 ]
Zheng, Ji-Shen [2 ,3 ]
Liu, Lei [4 ]
机构
[1] Qingdao Univ, Sch Pharm, Dept Med Chem, Qingdao 266073, Peoples R China
[2] Univ Sci & Technol China USTC, Affiliated Hosp 1, Dept Hematol, MOE Key Lab Membraneless Organelles & Cellular Dyn, Hefei 230001, Anhui, Peoples R China
[3] Univ Sci & Technol China, Hefei Natl Res Ctr Interdisciplinary Sci Microscal, Div Life Sci & Med, Hefei, Anhui, Peoples R China
[4] Tsinghua Univ, Dept Chem, Beijing 100084, Peoples R China
来源
CHEM | 2024年 / 10卷 / 08期
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
CHEMICAL-SYNTHESIS; MEMBRANE-PROTEINS; THIOESTER; ANTAGONIST; LIGATION; INHIBITION; CYSTEINE;
D O I
10.1016/j.chempr.2024.06.004
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Mirror-image proteins and peptides composed of D-amino acids are garnering increasing attention as diagnostic agents and drug candidates due to their higher stability and lower immunogenicity compared with their L-amino acid counterparts. The often-used strategy to discover mirror-image protein and peptide ligands of a native protein is the mirror-image phage display technique, in which the D-enantiomeric form of the L-target is used as the bait in phage display screening. Advancements in chemical protein synthesis have greatly facilitated the production of these D-protein targets, which are unattainable through recombinant expression technologies. This review spotlights recent developments in mirror-image protein and peptide drugs, focusing on the stateof-the-art synthetic methodologies that have been employed to acquire D-protein targets as well as the basic workflow and recent progress of mirror-image phage display and its applications to drug discovery.
引用
收藏
页码:2390 / 2407
页数:18
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