School of Chemistry, The University of Sydney, Sydney, NSW, Australia.
Australian Research Council Centre of Excellence for Innovations in Peptide and Protein Science, The University of Sydney, Sydney, NSW, Australia.
Methods Mol Biol. 2022;2530:125-140. doi: 10.1007/978-1-0716-2489-0_9.
Peptides bearing C-terminal thioester and selenoester functionalities are essential precursors for the chemical synthesis of larger proteins using ligation chemistry, including native chemical ligation (NCL) and diselenide-selenoester ligation (DSL). The use of a side-chain anchoring thioesterification or selenoesterification approach offers a robust method to access peptide thioesters or peptide selenoesters in excellent yields and in high purity. Importantly, this methodology overcomes solubility issues and epimerization of the C-terminal amino acid residue that can occur using solution-phase approaches. Detailed methods for the solid-phase synthesis of peptide thioesters and selenoesters using a side-chain anchoring approach are outlined in this article.
含有 C 末端硫酯和硒酯官能团的肽是使用连接化学(包括天然化学连接 (NCL) 和二硒代物-硒酯连接 (DSL))将较大蛋白质化学合成的重要前体。使用侧链锚定硫酯化或硒酯化方法提供了一种可靠的方法,可以以优异的收率和高纯度获得肽硫酯或肽硒酯。重要的是,该方法克服了使用溶液相方法可能发生的 C 末端氨基酸残基的溶解性问题和差向异构化。本文概述了使用侧链锚定方法在固相上合成肽硫酯和硒酯的详细方法。