Biomedical Engineering Department, Technology Faculty, Kocaeli University, 41380, Kocaeli, Turkey.
Department of Medical Biology, School of Medicine, Kocaeli University, 41380, Kocaeli, Turkey.
J Membr Biol. 2019 Dec;252(6):587-608. doi: 10.1007/s00232-019-00084-3. Epub 2019 Jul 25.
Plasma membrane proteins perform a variety of important tasks in the cells. These tasks can be diverse as carrying nutrients across the plasma membrane, receiving chemical signals from outside the cell, translating them into intracellular action, and anchoring the cell in a particular location. When these crucial roles of plasma membrane proteins are considered, the need for their characterization becomes inevitable. Certain characteristics of plasma membrane proteins such as hydrophobicity, low solubility, and low abundance limit their detection by proteomic analyses. Here, we presented a comparative proteomics study in which the most commonly used plasma membrane protein enrichment methods were evaluated. The methods that were utilized include biotinylation, selective CyDye labeling, temperature-dependent phase partition, and density-gradient ultracentrifugation. Western blot analysis was performed to assess the level of plasma membrane protein enrichment using plasma membrane and cytoplasmic protein markers. Quantitative evaluation of the level of enrichment was performed by two-dimensional electrophoresis (2-DE) and benzyldimethyl-n-hexadecylammonium chloride/sodium dodecyl sulfate polyacrylamide gel electrophoresis (16-BAC/SDS-PAGE) from which the protein spots were cut and identified. Results from this study demonstrated that density-gradient ultracentrifugation method was superior when coupled with 16-BAC/SDS-PAGE. This work presents a valuable contribution and provides a future direction to the membrane sub-proteome research by evaluating commonly used methods for plasma membrane protein enrichment.
质膜蛋白在细胞中执行各种重要任务。这些任务可以多种多样,例如将营养物质穿过质膜运输、从细胞外部接收化学信号、将其转化为细胞内的作用以及将细胞锚定在特定位置。考虑到质膜蛋白的这些关键作用,对其进行特征描述是不可避免的。质膜蛋白的某些特性,如疏水性、低溶解度和低丰度,限制了它们通过蛋白质组学分析的检测。在这里,我们进行了一项比较蛋白质组学研究,评估了最常用的质膜蛋白富集方法。所使用的方法包括生物素化、选择性 CyDye 标记、温度依赖性相分离和密度梯度超速离心。使用质膜和细胞质蛋白标记物进行 Western blot 分析,以评估质膜蛋白富集的水平。通过二维电泳(2-DE)和苄基二甲十六烷基氯化铵/十二烷基硫酸钠聚丙烯酰胺凝胶电泳(16-BAC/SDS-PAGE)进行定量评估,从该电泳中切取和鉴定蛋白点。这项研究的结果表明,当与 16-BAC/SDS-PAGE 结合使用时,密度梯度超速离心法更为优越。这项工作通过评估常用的质膜蛋白富集方法,为膜亚蛋白质组研究做出了有价值的贡献并提供了未来的方向。