Bruins Jorick J, van de Wouw Criss, Keijzer Jordi F, Albada Bauke, van Delft Floris L
Laboratory of Organic Chemistry, Wageningen University & Research, Wageningen, The Netherlands.
Methods Mol Biol. 2019;2012:357-368. doi: 10.1007/978-1-4939-9546-2_18.
Proteins can be labeled site-specifically and in inducible fashion by exposing a small peptide tag (GY) on any of its termini and activating the newly exposed tyrosine residue with the enzyme mushroom tyrosinase. The enzyme generates a quinone by oxidizing the tyrosine, which in turn can perform strain-promoted oxidation-controlled ortho-quinone cycloaddition (SPOCQ) with strained alkynes and alkenes, generating a stable conjugation product. Here, we describe a protocol to perform SPOCQ reaction on proteins, along with notes to optimize yield and reaction rates. Conjugation efficiencies of over 95% to antibodies have been reported using this protocol.
通过在蛋白质的任何一个末端暴露一个小肽标签(GY),并用蘑菇酪氨酸酶激活新暴露的酪氨酸残基,蛋白质可以被位点特异性地、以可诱导的方式进行标记。该酶通过氧化酪氨酸生成醌,醌进而可以与张力炔烃和烯烃进行应变促进的氧化控制邻醌环加成反应(SPOCQ),生成稳定的共轭产物。在此,我们描述了一种在蛋白质上进行SPOCQ反应的方案,以及优化产率和反应速率的注意事项。使用该方案已报道与抗体的共轭效率超过95%。