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Study of Prostate-Specific G Protein-Coupled Receptor Signalling in human LNCaP cells

机译:研究人LNCAP细胞中前列腺特异性G蛋白偶联受体信号传导

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a We successfully demonstrated that our phosphoproteomics strategy is well suited to identify phosphopeptides from orthovanadate-treated LNCaP cells. We were able to identify 2569 phosphorylation sites in 2095 phosphopeptides using as little as 200 μg of peptides in each of the two experiments. a Two different analysis platforms have been tested. Both platforms gave complementary results, while the Orbitrap/MaxQuant workflow performed best in respect to the amount of peptides and to the localisation site assignment. a A quantitative time course study of beta-ionone treated LNCaP cells resulted in the detection of 52 differentially regulated proteins. Amongst these proteins were components of the calcium homeostasis machinery as well as proteins associated with migration and cellular movement.
机译:A,我们成功地证明了我们的磷蛋白酶策略非常适合鉴定来自OrthovanaDate处理的LNCAP细胞的磷酸肽。我们能够在两个实验中的每一个中使用几乎200μg磷酸肽在2095个磷酸化物中鉴定2569位磷酸化位点。已经测试了两个不同的分析平台。两个平台都有互补的结果,而orbitrap / maxquant工作流程在肽的数量和本地化站点分配中表现最佳。 β离子处理的LNCAP细胞的定量时间课程研究导致检测52个差异调节的蛋白质。在这些蛋白质中是钙稳态机械的组分以及与迁移和细胞运动相关的蛋白质。

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