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Performance of different fractionation methods for quantitative proteomics analyses of membrane proteins from control and TNF-alpha activated mouse macrophages

机译:不同分馏方法对来自对照和TNF-α活性小鼠巨噬细胞的膜蛋白的定量蛋白质组学分析的性能

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In total, we identified 3103 unique proteins including 550 transmembrane proteins for all three fractionation methods. SCX provided the highest number of identified proteins. mRP and GelFREE fractionation appear to exhibit a slight advantage for quantitative proteomics analyses of membrane proteins in mouse macrophages - further evaluations ongoing. This study provides the most comprehensive analysis of the macrophage membrane proteome and provides interesting insights on the composition of the macrophage membrane compartment. The biological relevance of differentially regulated proteins upon TNF-alpha stimulation will be further examined and validated by cell biology methods.
机译:总共确定了3103个独特的蛋白质,包括所有三种分馏方法的550个跨膜蛋白。 SCX提供了最多数量的鉴定蛋白质。 MRP和Gelfree分馏似乎表现出小鼠巨噬细胞中膜蛋白的定量蛋白质组学分析的微量优势 - 进一步的评估正在进行中。 本研究提供了对巨噬细胞膜蛋白质组的最全面的分析,并对巨噬细胞膜隔室的组成提供有趣的见解。 通过细胞生物学方法进一步检查和验证差异调节蛋白质在TNF-α刺激上的生物学相关性。

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