Department of Cell Biology, Harvard Medical School, Boston, MA 02115, USA.
Department of Cell Biology, Harvard Medical School, Boston, MA 02115, USA.
Cell. 2020 Jan 23;180(2):387-402.e16. doi: 10.1016/j.cell.2019.12.023.
Proteins are essential agents of biological processes. To date, large-scale profiling of cell line collections including the Cancer Cell Line Encyclopedia (CCLE) has focused primarily on genetic information whereas deep interrogation of the proteome has remained out of reach. Here, we expand the CCLE through quantitative profiling of thousands of proteins by mass spectrometry across 375 cell lines from diverse lineages to reveal information undiscovered by DNA and RNA methods. We observe unexpected correlations within and between pathways that are largely absent from RNA. An analysis of microsatellite instable (MSI) cell lines reveals the dysregulation of specific protein complexes associated with surveillance of mutation and translation. These and other protein complexes were associated with sensitivity to knockdown of several different genes. These data in conjunction with the wider CCLE are a broad resource to explore cellular behavior and facilitate cancer research.
蛋白质是生物过程的重要介质。迄今为止,大规模的细胞系集合分析,包括癌症细胞系百科全书(CCLE),主要集中在遗传信息上,而对蛋白质组的深入研究仍然遥不可及。在这里,我们通过对来自不同谱系的 375 个细胞系进行质谱法的数千种蛋白质的定量分析,扩展了 CCLE,揭示了 DNA 和 RNA 方法未发现的信息。我们观察到了通路内和通路之间的意外相关性,这些相关性在 RNA 中基本上是不存在的。对微卫星不稳定(MSI)细胞系的分析表明,与突变和翻译监测相关的特定蛋白质复合物发生失调。这些和其他蛋白质复合物与几种不同基因敲低的敏感性有关。这些数据与更广泛的 CCLE 一起,是一个广泛的资源,可以用来探索细胞行为并促进癌症研究。