Department of Cellular & Molecular Medicine, University of California San Diego, La Jolla, CA, USA.
Methods Mol Biol. 2022;2438:123-131. doi: 10.1007/978-1-0716-2035-9_8.
Wnt proteins are secreted, lipid-modified growth factors with a wide range of activities across all metazoan species. Their production, secretion, and signaling range are under tight cellular control such that detection of Wnt proteins in biological samples is often extremely difficult. In this chapter, we describe a protocol to detect secreted Wnt proteins in the culture medium of cell lines that ectopically or endogenously express Wnt genes. This protocol uses an affinity resin, called Blue Sepharose, that binds and thereby enriches Wnt proteins, followed by immunoblotting for the Wnt protein of interest. This method for detecting Wnt proteins will aid in the isolation of biologically active Wnt proteins, provide an assay to study the molecular basis of Wnt secretion, and potentially offer a means to detect trace amounts of Wnt proteins associated with pathological states.
Wnt 蛋白是分泌型的脂修饰生长因子,在所有后生动物物种中具有广泛的活性。它们的产生、分泌和信号传递范围受到严格的细胞控制,因此在生物样本中检测 Wnt 蛋白通常非常困难。在本章中,我们描述了一种检测细胞系培养上清液中异位或内源性表达 Wnt 基因的 Wnt 蛋白的方法。该方案使用一种亲和树脂,称为 Blue Sepharose,它可以结合并富集 Wnt 蛋白,然后进行感兴趣的 Wnt 蛋白的免疫印迹分析。这种检测 Wnt 蛋白的方法将有助于分离具有生物活性的 Wnt 蛋白,提供研究 Wnt 分泌分子基础的分析方法,并可能提供一种检测与病理状态相关的痕量 Wnt 蛋白的方法。