Biological Science Division and Environmental Molecular Sciences Laboratory, Pacific Northwest National Laboratory, Richland, Washington 99352, USA.
J Proteome Res. 2009 Nov;8(11):5387-95. doi: 10.1021/pr900564f.
We report on a mouse specific SuperMix immunoaffinity separation system for separating low-abundance proteins from high and moderate abundance proteins in mouse plasma. When applied in tandem with a mouse IgY7 column that removes the seven most abundant proteins in plasma, the SuperMix column captures more than 100 additional moderate abundance proteins, thus allowing significant enrichment of low-abundance proteins in the flow-through fraction. A side-by-side comparison of results obtained from 2D-LC-MS/MS analyses of flow-through samples from IgY7 and SuperMix columns revealed a nearly 2-fold improvement in the overall proteome coverage. Detection of low-abundance proteins was also enhanced, as evidenced by a more than 2-fold increase in the coverage of cytokines, growth factors, and other low-abundance proteins. Moreover, the tandem separations are automated, reproducible, and allow effective identification of protein abundance differences from LC-MS/MS analyses. Considering the overall reproducibility and increased sensitivity using the IgY7-SuperMix separation system, we anticipate broad applications of this strategy for biomarker discovery using mouse models.
我们报告了一种针对小鼠的 SuperMix 免疫亲和分离系统,用于从小鼠血浆中的高丰度和中丰度蛋白中分离低丰度蛋白。当与去除血浆中七种最丰富蛋白的小鼠 IgY7 柱串联使用时,SuperMix 柱可捕获 100 多种额外的中丰度蛋白,从而使低丰度蛋白在流穿部分得到显著富集。对 IgY7 和 SuperMix 柱的流穿样品进行二维 LC-MS/MS 分析的结果进行了直接比较,发现整体蛋白质组覆盖率提高了近 2 倍。低丰度蛋白的检测也得到了增强,这表现在细胞因子、生长因子和其他低丰度蛋白的覆盖率增加了两倍以上。此外,串联分离是自动化的、可重现的,并且允许从 LC-MS/MS 分析中有效识别蛋白质丰度差异。考虑到使用 IgY7-SuperMix 分离系统的整体重现性和灵敏度提高,我们预计该策略将广泛应用于使用小鼠模型进行生物标志物发现。