Noaman Nour, Coorssen Jens R
Departments of Health Sciences and Biological Sciences, Faculties of Applied Health Sciences and Mathematics & Science, Brock University, St Catharines, Ontario, Canada.
Anal Biochem. 2018 Sep 1;556:53-56. doi: 10.1016/j.ab.2018.05.012. Epub 2018 Jun 28.
Quantitative comparative proteomics require accurate and reproducible assessments of total protein concentration. We report a straightforward, cost-effective adaptation of an established commercial method for total protein quantification (EZQ™), utilising non-proprietary materials and colloidal Coomassie Brilliant Blue (cCBB) staining to achieve greater reproducibility, equal sensitivity, and optimal linearity of signal within a practical concentration range for proteins in common solubilisation buffers (i.e. for isoelectric focussing and/or SDS-PAGE). This method provided more accurate and precise determinations of total protein concentration in human serum prepared for two-dimensional gel electrophoresis, indicating it may be better suited as the lead-in to most quantitative proteomic analyses.
定量比较蛋白质组学需要对总蛋白浓度进行准确且可重复的评估。我们报告了一种对已建立的总蛋白定量商业方法(EZQ™)进行的简单、经济高效的改进方法,该方法使用非专利材料和考马斯亮蓝胶体(cCBB)染色,以在常见溶解缓冲液(即用于等电聚焦和/或SDS-PAGE)中蛋白质的实际浓度范围内实现更高的重现性、同等灵敏度和最佳信号线性。该方法能更准确、精确地测定用于二维凝胶电泳的人血清中的总蛋白浓度,表明它可能更适合作为大多数定量蛋白质组学分析的先导方法。