电泳剂
共价键
组合化学
化学
化学空间
化学生物学
分子内力
药物发现
亲核细胞
计算生物学
肽库
肽
序列(生物学)
纳米技术
配体(生物化学)
动态共价化学
亲核芳香族取代
计算机科学
立体化学
拟肽
连接器
合成生物学
作者
Joy Walker,Kejia Yan,Ratmir Derda
出处
期刊:Biochemistry
[American Chemical Society]
日期:2026-01-08
卷期号:65 (2): 149-165
标识
DOI:10.1021/acs.biochem.5c00646
摘要
Peptide-derived macrocycles are an emerging class of therapeutics capable of modulating protein-protein interactions that remain inaccessible to small molecules. Genetically encoded library (GEL) platforms such as phage and mRNA display have accelerated macrocyclic ligand discovery by linking peptide sequence to genotype and enabling selections from libraries with up to 1013 members. Efforts to expand the chemical space of GELs have included incorporation of electrophiles, either to generate libraries of true covalent ligands or to enable intramolecular reactions such as peptide cyclization. In the latter case, the electrophile is consumed during library construction, producing transient covalent libraries that enhance stability and diversity but are not designed for direct covalent engagement with targets. By contrast, recent advances have established robust strategies for embedding persistent electrophilic warheads that remain intact during library preparation and selectively react with nucleophilic residues on proteins. These approaches have yielded both reversible and irreversible covalent inhibitors against diverse classes of proteins, while also highlighting challenges in balancing electrophile reactivity with library integrity. Complementary developments in DNA-encoded covalent libraries further underscore the breadth of discovery platforms, though genetically encoded approaches remain uniquely powerful for macrocyclic peptides. Together, these advances define the trajectory of covalent genetically encoded libraries (cGELs) and point toward new opportunities for discovering ligands to historically undruggable targets.
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