Rhodes Curran A, Pei Dehua
Department of Chemistry and Biochemistry, The Ohio State University, 484 West 12th Avenue, Columbus, Ohio, 43210, USA.
Chemistry. 2017 Sep 18;23(52):12690-12703. doi: 10.1002/chem.201702117. Epub 2017 Jul 27.
Bicyclic peptides have greater conformational rigidity and metabolic stability than linear and monocyclic peptides and are capable of binding to challenging drug targets with antibody-like affinity and specificity. Powerful combinatorial library technologies have recently been developed to rapidly synthesize and screen large bicyclic peptide libraries for ligands against enzymes, receptors, and protein-protein interaction targets. Bicyclic peptides have been developed as potential therapeutics against a wide range of diseases, drug targeting agents, imaging/diagnostic probes, and research tools. In this Minireview, we provide a summary of the recent progresses on the synthesis and applications of bicyclic peptides.
双环肽比线性和单环肽具有更高的构象刚性和代谢稳定性,并且能够以类似抗体的亲和力和特异性与具有挑战性的药物靶点结合。最近已经开发出强大的组合文库技术,用于快速合成和筛选针对酶、受体和蛋白质-蛋白质相互作用靶点的配体的大型双环肽文库。双环肽已被开发为针对多种疾病的潜在治疗药物、药物靶向剂、成像/诊断探针和研究工具。在本综述中,我们总结了双环肽合成和应用的最新进展。