Quintana-Hayashi Macarena P, Lindén Sara K
Department of Medical Biochemistry and Cell Biology, Institute of Biomedicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Methods Mol Biol. 2025;2942:157-163. doi: 10.1007/978-1-0716-4627-4_13.
Here, we describe a method that detects bacterial binding to mucus on slot-blot membranes. Mucins, the large, highly glycosylated proteins forming the mucus gel, attach slower to microwell plates than the small less glycosylated components of mucus, which quickly coat plastic surfaces and thereby limit mucin attachment. Therefore, other methods are necessary to retain significant levels of mucins when performing assays on mixed samples. In the method described here, samples are dot-blotted onto a polyvinylidene fluoride membrane and incubated with biotinylated bacteria. Bacterial adhesion to mucins is determined after visualization of the slot-blots with an infrared imaging system and quantification of the image pixel intensities. This method is also useful for the detection of bacterial binding to enzyme-treated mucins, for example with sialidase, and binding intensities can be compared to nonenzyme (mock)-treated mucins.
在此,我们描述了一种检测细菌与狭缝印迹膜上黏液结合的方法。黏蛋白是形成黏液凝胶的大型高度糖基化蛋白质,其附着到微孔板上的速度比黏液中糖基化程度较低的小成分慢,这些小成分会迅速覆盖塑料表面,从而限制黏蛋白的附着。因此,在对混合样本进行检测时,需要其他方法来保留大量的黏蛋白。在此描述的方法中,将样本点印迹到聚偏二氟乙烯膜上,并用生物素化细菌孵育。在用红外成像系统对狭缝印迹进行可视化并对图像像素强度进行定量后,确定细菌对黏蛋白的黏附。该方法对于检测细菌与经酶处理的黏蛋白(例如用唾液酸酶处理)的结合也很有用,并且可以将结合强度与未经酶(模拟)处理的黏蛋白进行比较。