化学
差向异构体
位阻效应
天然化学连接
结扎
肽
内酯
化学结扎
硫酯
组合化学
水解
立体化学
生物化学
化学合成
有机化学
酶
分子生物学
体外
生物
作者
Xinhao Fan,Yuming Wen,Huan Chen,Baotong Tian,Qiang Zhang
出处
期刊:Organic Letters
[American Chemical Society]
日期:2024-06-20
卷期号:26 (26): 5436-5440
标识
DOI:10.1021/acs.orglett.4c01587
摘要
Native chemical ligation (NCL) represents a cornerstone strategy in accessing synthetic peptides and proteins, remaining one of the most efficacious methodologies in this domain. The fundamental requisites for achieving a proficient NCL reaction involve chemoselective coupling between a C-terminal thioester peptide and a thiol-bearing N-terminal peptide. However, achieving coupling at sterically congested residues remains challenging. In addition, while most NCLs proceed without epimerization, β-branched (e.g., Ile, Thr, Val) and Pro-derived C-terminal thioesters react slowly and can be susceptible to significant epimerization and hydrolysis. Herein, we report an epimerization-free NCL reaction via β-lactone-mediated native chemical ligation which constructs sterically congested Thr residues. The constrained ring from the β-lactone allows rapid peptide ligation without detectable epimerization. The method has a broad side-chain tolerance and was applied to the preparation of cyclic peptides and polypeptidyl thioester, which could be difficult to obtained otherwise.
科研通智能强力驱动
Strongly Powered by AbleSci AI