Plateforme Protéomique Strasbourg-Esplanade FRC 1589, Université de Strasbourg, Centre National de la Recherche Scientifique, F-67000, France.
RIDI UPR 9022, Université de Strasbourg, Centre National de la Recherche Scientifique, F-67000, France.
G3 (Bethesda). 2017 Jul 5;7(7):2249-2258. doi: 10.1534/g3.117.042564.
Receptor for Activated protein C kinase 1 (RACK1) is a scaffold protein that has been found in association with several signaling complexes, and with the 40S subunit of the ribosome. Using the model organism , we recently showed that RACK1 is required at the ribosome for internal ribosome entry site (IRES)-mediated translation of viruses. Here, we report a proteomic characterization of the interactome of RACK1 in S2 cells. We carried out Label-Free quantitation using both Data-Dependent and Data-Independent Acquisition (DDA and DIA, respectively) and observed a significant advantage for the Sequential Window Acquisition of all THeoretical fragment-ion spectra (SWATH) method, both in terms of identification of interactants and quantification of low abundance proteins. These data represent the first SWATH spectral library available for and will be a useful resource for the community. A total of 52 interacting proteins were identified, including several molecules involved in translation such as structural components of the ribosome, factors regulating translation initiation or elongation, and RNA binding proteins. Among these 52 proteins, 15 were identified as partners by the SWATH strategy only. Interestingly, these 15 proteins are significantly enriched for the functions translation and nucleic acid binding. This enrichment reflects the engagement of RACK1 at the ribosome and highlights the added value of SWATH analysis. A functional screen did not reveal any protein sharing the interesting properties of RACK1, which is required for IRES-dependent translation and not essential for cell viability. Intriguingly however, 10 of the RACK1 partners identified restrict replication of Cricket paralysis virus (CrPV), an IRES-containing virus.
激活蛋白 C 激酶 1(RACK1)受体是一种支架蛋白,已发现它与几种信号复合物以及核糖体的 40S 亚基有关。使用模式生物,我们最近表明 RACK1 在核糖体上对于内部核糖体进入位点(IRES)介导的病毒翻译是必需的。在这里,我们报告了 RACK1 在 S2 细胞中相互作用组的蛋白质组学特征。我们使用无标记定量法(分别为 DDA 和 DIA)进行了定量,并观察到 SWATH 方法在鉴定相互作用体和定量低丰度蛋白方面具有明显优势。这些数据代表了首个适用于的 SWATH 光谱库,将成为社区的有用资源。总共鉴定出 52 个相互作用蛋白,包括几个参与翻译的分子,如核糖体的结构成分、调节翻译起始或延伸的因子以及 RNA 结合蛋白。在这 52 个蛋白中,有 15 个是通过 SWATH 策略仅鉴定为伴侣的。有趣的是,这 15 个蛋白在翻译和核酸结合功能上显著富集。这种富集反映了 RACK1 在核糖体上的参与,并突出了 SWATH 分析的附加值。功能筛选没有发现任何与 RACK1 具有有趣特性的蛋白质共享,而 RACK1 是 IRES 依赖性翻译所必需的,对细胞活力不是必需的。然而,有趣的是,鉴定出的 10 个 RACK1 伴侣限制了 Cricket 麻痹病毒(CrPV)的复制,CrPV 是一种含有 IRES 的病毒。