Targeting of extracellular protein-protein interactions with macrocyclic peptides

被引:12
|
作者
Taguchi, Shota [1 ]
Suga, Hiroaki [2 ]
机构
[1] Univ Tokyo, Grad Sch Engn, Dept Adv Interdisciplinary, Bunkyo Ku, 7-3-1 Hongo, Tokyo 1130033, Japan
[2] Univ Tokyo, Grad Sch Sci, Dept Chem, Bunkyo Ku, 7-3-1 Hongo, Tokyo 1130033, Japan
基金
日本学术振兴会;
关键词
Macrocyclic peptide; Protein protein interaction; Drug discovery; Extracellular protein; HISTIDINE KINASE; INHIBITION; MECHANISMS; MET;
D O I
10.1016/j.cbpa.2021.02.013
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Targeting of extracellular protein-protein interactions (PPI) is emerging as a major application for de novo discovered macrocyclic peptides. Modern discovery platforms can routinely identify macrocyclic peptide ligands capable of highly selective modulation of extracellular signaling pathways; amenability to chemical synthesis and natural modularity of peptides additionally provides an avenue for their further structural elaboration, while the challenge of cell internalization can be minimized. Here, we discuss the recent progress in targeting extracellular PPIs with macrocyclic peptides by focusing on a number of recent case studies. We analyze the scope and potential limitations of the discovery systems in identifying functional macrocyclic ligands. We also highlight the recent technical advancements allowing for a more streamlined discovery pipeline and our brief perspective in this field.
引用
收藏
页码:82 / 89
页数:8
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