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含氮杂环丙烷四肽的固相合成、环化和定点功能化。

Solid-phase synthesis, cyclization, and site-specific functionalization of aziridine-containing tetrapeptides.

机构信息

NuChem Therapeutics, Montréal, Québec, Canada.

Laboratorium für Organische Chemie, Department of Chemistry and Applied Biosciences, ETH Zürich, Zürich, Switzerland.

出版信息

Nat Protoc. 2017 Jun;12(6):1277-1287. doi: 10.1038/nprot.2017.035. Epub 2017 May 24.

Abstract

Cyclic tetrapeptides comprise a potent and selective class of molecules with a wide range of biological activities, including the phytotoxic activity of tentoxin and the histone deacetylase (HDAC) inhibitory effects of chlamydocin. The incorporation of a functional aziridine group within cyclic peptides enables their conformational control and allows for late-stage and site-selective functionalization of these molecules, thereby creating the potential for covalent protein labeling. This protocol describes the solid-phase synthesis, cyclization, and site-specific structural modification of aziridine-containing tetrapeptides. The linear precursors are assembled by solid-phase peptide synthesis using Fmoc-protected amino acid building blocks, followed by head-to-tail peptide cyclization. Cyclization is performed using a slow reverse-addition method that prevents the formation of undesired higher-order cyclo-oligomeric side products. Site-specific structural modification of the resulting macrocycles is described using sodium azide or thiophenol as representative examples. It requires ∼4 d to prepare peptide macrocycles from their respective Fmoc-protected amino acid starting materials, an improvement upon the 3 weeks required for conventional solution-phase methods. This protocol also addresses important considerations regarding the handling of these compounds, whose electrophilic aziridine functionalities can otherwise be prone to undesired side reactions. With recent developments in aziridine-containing macrocyclic peptide synthesis and the potential for covalent protein labeling, these scaffolds represent a valuable addition to many screening libraries, and we expect that access to these macrocycles will facilitate efforts in drug discovery and molecular probe development.

摘要

环状四肽是一类具有广泛生物活性的强效和选择性分子,包括 tentoxin 的植物毒性活性和 chlamydocin 的组蛋白去乙酰化酶 (HDAC) 抑制作用。在环状肽中引入功能化氮丙啶基团可以控制其构象,并允许对这些分子进行晚期和位点选择性的功能化,从而为共价蛋白质标记创造了潜力。本协议描述了含氮丙啶四肽的固相合成、环化和位点特异性结构修饰。线性前体通过固相肽合成使用 Fmoc 保护的氨基酸砌块组装,然后进行头到尾肽环化。环化采用缓慢反向添加方法进行,可防止形成不需要的高阶环寡聚物副产物。使用叠氮化钠或苯硫酚作为代表性示例描述了所得大环的位点特异性结构修饰。从各自的 Fmoc 保护氨基酸起始原料制备肽大环大约需要 4 天,比传统的溶液相方法所需的 3 周时间有所改进。本协议还解决了处理这些化合物的重要注意事项,其亲电氮丙啶官能团否则容易发生不需要的副反应。随着含氮丙啶大环肽合成的最新发展和共价蛋白质标记的潜力,这些支架为许多筛选文库增添了有价值的内容,我们预计这些大环的获得将有助于药物发现和分子探针开发的努力。

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