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Comparative untargeted proteomic analysis of ADME proteins and tumor antigens for tumor cell lines

机译:针对肿瘤细胞系的ADME蛋白和肿瘤抗原的比较性非靶向蛋白质组学分析

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摘要

In the present study, total membrane proteins from tumor cell lines including HepG2, Hep3B2, H226, Ovcar3 and N87 were extracted and digested with γLysC and trypsin. The resulting peptide lysate were pre-fractionated and subjected to untargeted quantitative proteomics analysis using a high resolution mass spectrometer. The mass spectra were processed by the MaxQuant and the protein abundances were estimated using total peak area (TPA) method. A total of 6037 proteins were identified, and the analysis resulted in the identification of 2647 membrane proteins. Of those, tumor antigens and absorption, metabolism, disposition and elimination (ADME) proteins including UDP-glucuronosyltransferase, cytochrome P450, solute carriers and ATP-binding cassette transporters were detected and disclosed significant variations among the cell lines. The principal component analysis was performed for the cluster of cell lines. The results demonstrated that H226 is closely related with N87, while Hep3B2 aligned with HepG2. The protein cluster of Ovcar3 was apart from that of other cell lines investigated. By providing for the first time quantitative untargeted proteomics analysis, the results delineated the expression profiles of membrane proteins. These findings provided a useful resource for selecting targets of choice for anticancer therapy through advancing data obtained from preclinical tumor cell line models to clinical outcomes.
机译:在本研究中,从包括HepG2,Hep3B2,H226,Ovcar3和N87在内的肿瘤细胞系中提取总膜蛋白,并用γLysC和胰蛋白酶消化。将所得的肽裂解物预先分级分离,并使用高分辨率质谱仪进行非目标定量蛋白质组学分析。通过MaxQuant处理质谱,并使用总峰面积(TPA)方法估算蛋白质丰度。总共鉴定出6037种蛋白质,分析结果鉴定出2647种膜蛋白质。其中,检测到肿瘤抗原和吸收,代谢,处置和消除(ADME)蛋白,包括UDP-葡萄糖醛酸糖基转移酶,细胞色素P450,溶质载体和ATP结合盒转运蛋白,并揭示了细胞系之间的显着差异。对细胞系簇进行主成分分析。结果表明H226与N87密切相关,而Hep3B2与HepG2对齐。 Ovcar3的蛋白质簇与其他研究的细胞系不同。通过首次提供定量的非靶向蛋白质组学分析,结果描绘了膜蛋白的表达谱。这些发现为将临床前肿瘤细胞系模型获得的数据推进到临床结果提供了有用的资源,用于选择抗癌治疗的靶标。

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