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用2-叠氮基丙烯酸酯对肽和蛋白质中的半胱氨酸残基进行位点特异性双功能化修饰

Site-Specific Dual Functionalization of Cysteine Residue in Peptides and Proteins with 2-Azidoacrylates.

作者信息

Ariyasu Shinya, Hayashi Hirohito, Xing Bengang, Chiba Shunsuke

机构信息

Division of Chemistry and Biological Chemistry, School of Physical and Mathematical Sciences, Nanyang Technological University , 637371 Singapore.

出版信息

Bioconjug Chem. 2017 Apr 19;28(4):897-902. doi: 10.1021/acs.bioconjchem.7b00024. Epub 2017 Feb 21.

Abstract

Herein, we report use of 2-azidoacrylates to perform site-specific dual functionalization of the cysteine residue of peptides and bovine serum albumin (BSA), a native protein containing one free cysteine residue. The sulfhydryl group of the cysteine residue could be conjugated with 2-azidoacrylates bearing various functionalities, such as fluorescent dyes under physiological aqueous buffer conditions, to afford peptide and protein conjugates anchoring an azide moiety. Successive azide-alkyne cycloaddition enables installation of the second functionality, thus affording dual-functionalized peptide- and protein-based materials.

摘要

在此,我们报道了使用2-叠氮基丙烯酸酯对肽和牛血清白蛋白(BSA,一种含有一个游离半胱氨酸残基的天然蛋白质)的半胱氨酸残基进行位点特异性双功能化。在生理水性缓冲条件下,半胱氨酸残基的巯基可与带有各种功能基团(如荧光染料)的2-叠氮基丙烯酸酯共轭,从而得到带有叠氮基部分的肽和蛋白质共轭物。连续的叠氮化物-炔烃环加成反应能够引入第二种功能基团,从而得到双功能化的基于肽和蛋白质的材料。

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