Department of Pathology and Anatomical Sciences, University of Missouri School of Medicine, Columbia, MO, USA.
Ellis Fischel Cancer Center, University of Missouri School of Medicine, Columbia, MO, USA.
Prep Biochem Biotechnol. 2023 Nov;53(10):1243-1253. doi: 10.1080/10826068.2023.2185897. Epub 2023 Mar 17.
Western blot analysis of relative protein expression relies on appropriate reference proteins for data normalization. Small extracellular vesicles (sEVs), or exosomes, are increasingly recognized as potential indicators of the physiological state of cells due to their protein composition. Therefore, accurate relative sEVs protein quantification is crucial for disease detection and prognosis applications. Currently, no documented ubiquitous reference proteins are identified for precise normalization of a protein of interest in sEVs. Here we showed the use of total protein staining method for sEVs protein normalization in western blots of samples where conventional housekeeping proteins like β-actin and glyceraldehyde 3-phosphate dehydrogenase (GAPDH) are not always detected in the sEVs western blots. The No-Stain™ Protein Labeling (NSPL) method showed high sensitivity in sEVs-protein labeling and facilitated quantitative evaluation of changes in the expression pattern of the protein of interest. Further, to show the robustness of NSPL for expression analysis, the results were compared with quantitative mass spectroscopy analysis results. Here, we outline a comprehensive method for protein normalization in sEVs that will increase the value of protein expression study of therapeutically significant sEVs.
Western blot 分析相对蛋白表达依赖于适当的参照蛋白进行数据归一化。由于其蛋白质组成,小细胞外囊泡(sEVs)或外泌体越来越被认为是细胞生理状态的潜在标志物。因此,准确相对 sEVs 蛋白定量对于疾病检测和预后应用至关重要。目前,尚未确定普遍存在的参照蛋白,以精确归一化 sEVs 中感兴趣的蛋白。在这里,我们展示了总蛋白染色法在 Western blot 中的应用,用于 sEVs 蛋白归一化,在 Western blot 中,常规管家蛋白如β-肌动蛋白和甘油醛 3-磷酸脱氢酶(GAPDH)并不总是在 sEVs Western blot 中检测到。No-Stain™ Protein Labeling(NSPL)方法在 sEVs 蛋白标记中具有高灵敏度,并促进了感兴趣蛋白表达模式变化的定量评估。此外,为了显示 NSPL 用于表达分析的稳健性,将结果与定量质谱分析结果进行了比较。在这里,我们概述了一种全面的 sEVs 蛋白归一化方法,将增加治疗意义上的 sEVs 蛋白表达研究的价值。