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Comparative Proteomic Profiling of Unannotated Microproteins and Alternative Proteins in Human Cell Lines

机译:未泛型的微蛋白和人细胞系中替代蛋白的比较蛋白质组学分析

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摘要

Ribosome profiling and mass spectrometry have revealed thousands of small and alternative open reading frames (sm/alt-ORFs) that are translated into polypeptides variously termed as microproteins and alt-proteins in mammalian cells. Some micro-/alt-proteins exhibit stress-, cell-type-, and/or tissue-specific expression; understanding this regulated expression will be critical to elucidating their functions. While differential translation has been inferred by ribosome profiling, quantitative mass spectrometry-based proteomics is needed for direct comparison of microprotein and alt-protein expression between samples and conditions. However, while label-free quantitative proteomics has been applied to detect stress-dependent expression of bacterial microproteins, this approach has not yet been demonstrated for analysis of differential expression of unannotated ORFs in the more complex human proteome. Here, we present global micro-/alt-protein quantitation in two human leukemia cell lines, K562 and MOLT4. We identify 12 unannotated proteins that are differentially expressed in these cell lines. The expression of six micro/alt-proteins from cDNA was validated biochemically, and two were found to localize to the nucleus. Thus, we demonstrate that label-free comparative proteomics enables quantitation of micro-/alt-protein expression between human cell lines. We anticipate that this workflow will enable the discovery of regulated sm/alt-ORF products across many biological conditions in human cells.
机译:核糖体的分析和质谱揭示了数千名的小和替代的开放阅读框(SM / ALT-ORF),其被称为不同称为哺乳动物细胞中的微蛋白和Alt-蛋白的多肽。一些微/ Alt-蛋白表现出应力,细胞型和/或组织特异性表达;了解这一规范表达对阐明其功能至关重要。虽然通过核糖体分析推断出差异翻译,但需要定量质谱蛋白质组学,用于直接比较样品和条件之间的微蛋白和ALT-蛋白表达。然而,虽然已经应用无标记的定量蛋白质组学来检测细菌微蛋白的应力依赖性表达,但该方法尚未证明用于分析未复杂的人蛋白质组中未经发道的ORF的差异表达。在这里,我们在两种人白血病细胞系,K562和MOLT4中呈现全球微/ ALT-蛋白质定量。我们鉴定12个未在这些细胞系中差异表达的未烧结蛋白质。将来自cDNA的六种微/醇蛋白的表达被生物化学验证,发现两种局部化为核。因此,我们证明了无标记的比较蛋白质组学能够定量人细胞系之间的微/ Alt蛋白表达。我们预计此工作流程将在人类细胞中许多生物条件下发现受管制的SM / ALT-ORF产品。

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