Vinogradov Alexander A, Suga Hiroaki
Department of Chemistry, Graduate School of Science, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-0033, Japan.
Cell Chem Biol. 2020 Aug 20;27(8):1032-1051. doi: 10.1016/j.chembiol.2020.07.003. Epub 2020 Jul 21.
Thiopeptides (also known as thiazolyl peptides) are structurally complex natural products with rich biological activities. Known for over 70 years for potent killing of Gram-positive bacteria, thiopeptides are experiencing a resurgence of interest in the last decade, primarily brought about by the genomic revolution of the 21st century. Every area of thiopeptide research-from elucidating their biological function and biosynthesis to expanding their structural diversity through genome mining-has made great strides in recent years. These advances lay the foundation for and inspire novel strategies for thiopeptide engineering. Accordingly, a number of diverse approaches are being actively pursued in the hope of developing the next generation of natural-product-inspired therapeutics. Here, we review the contemporary understanding of thiopeptide biological activities, biosynthetic pathways, and approaches to structural and functional reprogramming, with a special focus on the latter.
硫肽(也称为噻唑基肽)是一类结构复杂且具有丰富生物活性的天然产物。硫肽因对革兰氏阳性菌有强大的杀伤作用而被人们所熟知,至今已有70多年的历史,在过去十年中,由于21世纪的基因组革命,人们对硫肽的兴趣再度兴起。近年来,硫肽研究的各个领域——从阐明其生物学功能和生物合成,到通过基因组挖掘扩展其结构多样性——都取得了长足的进展。这些进展为硫肽工程奠定了基础,并激发了新的策略。因此,人们正在积极探索多种不同的方法,以期开发出下一代受天然产物启发的治疗药物。在此,我们综述了对硫肽生物活性、生物合成途径以及结构和功能重新编程方法的当代理解,特别关注后者。