化学
环肽
脚手架
组合化学
药物发现
肽
化学合成
肽合成
核糖体RNA
固相合成
生物合成
氨基酸
核糖体蛋白
抗菌活性
抗菌剂
天然产物
合成生物学
生物化学
乌吉反应
肽生物合成
生物活性
纳米技术
抗菌肽
代谢稳定性
细菌
抗菌肽
吞吐量
计算生物学
氨基酸残基
化学生物学
立体化学
作者
Feng Wan,Chen Hu,Pei Xie,Xingxing Yang,Xin He,Yourong Pan,Zuozhou Ning,Chengxi Li
摘要
Cyclic peptides uniquely integrate the structural stability and target specificity of biologics with the synthetic versatility of small molecules. However, their chemical synthesis has historically lagged behind ribosomal production in both speed and efficiency. Herein, we present CycloBot, a robotic platform designed for fully automated, minute-scale assembly of cyclopeptides, approaching the throughput of ribosomal biosynthesis while accommodating both natural and non-natural amino acids. Central to this advancement is a diaminonicotinic acid (DAN) scaffold enabling “one-click”, concomitant cyclization/cleavage head-to-tail cyclization directly on resin, affording macrocycles of varying sizes with yields up to 93%, crude purities exceeding 95%, and minimal epimerization. The platform’s utility is exemplified by the rapid generation of a 20-member antimicrobial cyclic peptide library in 1 day, from which a lead candidate exhibited 100-fold enhanced antibacterial activity against S. aureus and B. subtilis relative to penicillin. By bridging the speed of ribosomal synthesis and the structural diversity accessible via chemical synthesis, this technology establishes a new paradigm for accelerated discovery and development of personalized cyclic peptide therapeutics.
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