Faculty of Pharmaceutical Sciences, Hokkaido University, Kita 12, Nishi 6, Kita-ku, Sapporo 060-0812, Japan.
Curr Opin Chem Biol. 2024 Jun;80:102465. doi: 10.1016/j.cbpa.2024.102465. Epub 2024 May 17.
Macrocyclization of peptides reduces conformational flexibilities, potentially leading to improved drug-like properties, such as target specificities and metabolic stabilities. As chemical methodologies often allow side reactions like epimerization and oligomerization, keen attention has been directed toward enzymatic peptide cyclization using peptide cyclases from specialized metabolic pathways. Penicillin-binding protein-type thioesterases (PBP-type TEs) are a recently identified family of peptide cyclases involved in the biosynthesis of non-ribosomal peptides in actinobacteria. PBP-type TEs have undergone intensive investigation due to their outstanding potential as biocatalysts. This review summarizes the rapidly growing knowledge on PBP-type TEs, with special emphasis on their functions, scopes, and structures, and efforts towards their biocatalytic applications.
环肽化可以降低构象灵活性,从而可能改善药物样性质,如靶标特异性和代谢稳定性。由于化学方法通常允许发生类似差向异构化和寡聚化等副反应,因此人们一直密切关注使用来自专门代谢途径的肽环化酶对肽进行酶促环化。青霉素结合蛋白型硫酯酶(PBP 型 TE)是最近在放线菌中非核糖体肽生物合成中发现的一种肽环化酶家族。由于其作为生物催化剂的巨大潜力,PBP 型 TE 受到了广泛的研究。本文综述了 PBP 型 TE 的快速发展知识,特别强调了它们的功能、范围和结构,以及它们在生物催化应用方面的努力。