Tuladhar Rubina, Yarravarapu Nageswari, Lum Lawrence
Department of Cell Biology, University of Texas Southwestern Medical Center, NL07.138B, 5323 Harry Hines Blvd., Dallas, TX, 75390-9039, USA.
Methods Mol Biol. 2016;1481:11-6. doi: 10.1007/978-1-4939-6393-5_2.
We describe here a technique for visualizing the lipidation status of Wnt proteins using azide-alkyne cycloaddition chemistry (click chemistry) and SDS-PAGE. This protocol incorporates in vivo labeling of a Wnt-IgG Fc fusion protein using an alkynylated palmitate probe but departs from a traditional approach by incorporating a secondary cycloaddition reaction performed on single-step purified Wnt protein immobilized on protein A resin. This approach mitigates experimental noise by decreasing the contribution of labeling from other palmitoylated proteins and by providing a robust method for normalizing labeling efficiency based on protein abundance.
我们在此描述一种利用叠氮化物-炔烃环加成化学(点击化学)和十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)来可视化Wnt蛋白脂化状态的技术。该方案采用炔基化棕榈酸酯探针在体内标记Wnt-IgG Fc融合蛋白,但与传统方法不同的是,它对固定在蛋白A树脂上的单步纯化Wnt蛋白进行二次环加成反应。这种方法通过减少其他棕榈酰化蛋白标记的贡献,并提供一种基于蛋白丰度来标准化标记效率的可靠方法,从而减轻实验噪音。