Departments of Physiology & Biophysics and Developmental & Cell Biology, University of California, Irvine, California 92697, USA.
Mol Cell Proteomics. 2012 May;11(5):138-47. doi: 10.1074/mcp.M111.016352. Epub 2012 Apr 3.
The COP9 signalosome (CSN) is a multi-subunit protein complex that performs critical roles in controlling diverse cellular and developmental processes. Aberrant regulation of the CSN complex has been shown to lead to tumorigenesis. Despite its biological significance, our current knowledge of the function and regulation of the CSN complex is very limited. To explore CSN biology, we have developed and employed a new version of the tag team-based QTAX strategy (quantitative analysis of tandem affinity purified in vivo cross-linked (X) protein complexes) by incorporating a label-free MS method for quantitation. Coupled with protein interaction network analysis, this strategy produced a comprehensive and detailed assessment of the protein interaction network of the human CSN complex. In total, we quantitatively characterized 825 putative CSN-interacting proteins, with 270 classified as core interactors (captured by all three bait purifications). Biochemical validation further confirms the validity of selected identified interactors. This work presents the most complete analysis of the CSN interaction network to date, providing an inclusive set of physical interaction data consistent with physiological roles for the CSN. Moreover, the methodology described here is a general proteomic tool for the comprehensive study of protein interaction networks.
COP9 信号小体(CSN)是一种多亚基蛋白复合物,在控制多种细胞和发育过程中发挥着关键作用。CSN 复合物的异常调节已被证明会导致肿瘤发生。尽管 CSN 复合物具有重要的生物学意义,但我们目前对其功能和调节的了解非常有限。为了探索 CSN 生物学,我们开发并采用了一种新的基于标签对的 QTAX 策略(基于串联亲和纯化的体内交联(X)蛋白复合物的定量分析),该策略结合了一种无标签 MS 方法进行定量。结合蛋白质相互作用网络分析,该策略对人 CSN 复合物的蛋白质相互作用网络进行了全面和详细的评估。总共定量表征了 825 种假定的 CSN 相互作用蛋白,其中 270 种被归类为核心相互作用蛋白(通过三种诱饵纯化都能捕获)。生化验证进一步证实了所选鉴定的相互作用蛋白的有效性。这项工作代表了迄今为止对 CSN 相互作用网络最全面的分析,提供了一套完整的物理相互作用数据,与 CSN 的生理作用一致。此外,这里描述的方法是一种通用的蛋白质组学工具,可用于全面研究蛋白质相互作用网络。