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N,O-苄叉缩二肽(NBDs)通过弯曲骨架策略实现了困难肽的合成。

N,O-Benzylidene Acetal Dipeptides (NBDs) Enable the Synthesis of Difficult Peptides via a Kinked Backbone Strategy.

机构信息

Department of Chemistry, State Key Laboratory of Synthetic Chemistry, The University of Hong Kong, Pokfulam Road, Hong Kong SAR, P. R. China.

Laboratory for Marine Drugs and Bioproducts, Qingdao National Laboratory for Marine Science and Technology, School of Medicine and Pharmacy, Ocean University of China, Qingdao, 266003, P. R. China.

出版信息

Angew Chem Int Ed Engl. 2023 Oct 26;62(44):e202310624. doi: 10.1002/anie.202310624. Epub 2023 Sep 20.

Abstract

Proteins with highly hydrophobic regions or aggregation-prone sequences are typically difficult targets for chemical synthesis at the current stage, as obtaining such type of peptides via solid-phase peptide synthesis requires sophisticated operations. Herein, we report N,O-benzylidene acetal dipeptides (NBDs) as robust and effective building blocks to allow the direct synthesis of difficult peptides and proteins via a kinked backbone strategy. The effectiveness and easy accessibility of NBDs have been well demonstrated in our chemical syntheses of various challenging peptides and proteins, including chemokine, therapeutic hormones, histone, and glycosylated erythropoietin.

摘要

具有高度疏水区或易于聚集序列的蛋白质在当前阶段通常是化学合成的难点,因为通过固相肽合成获得此类肽需要复杂的操作。在此,我们报告 N,O-亚苄基缩醛二肽(NBD)作为坚固有效的构建块,可通过扭曲的骨架策略直接合成困难的肽和蛋白质。NBD 的有效性和易于获得性已在我们对各种具有挑战性的肽和蛋白质的化学合成中得到了很好的证明,包括趋化因子、治疗性激素、组蛋白和糖基化促红细胞生成素。

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