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首页> 外文期刊>Journal of proteome research >Deep Coverage Proteomics Identifies More Low-Abundance Missing Proteins in Human Testis Tissue with Q-Exactive HF Mass Spectrometer
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Deep Coverage Proteomics Identifies More Low-Abundance Missing Proteins in Human Testis Tissue with Q-Exactive HF Mass Spectrometer

机译:深度覆盖蛋白质组学使用Q活性HF质谱仪鉴定人睾丸组织中更多的低丰度缺失蛋白

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摘要

Since 2012, missing proteins (MPs) investigation has been one of the critical missions of Chromosome-Centric Human Proteome Project (C-HPP) through various biochemical strategies. On the basis of our previous testis MPs study, faster scanning and higher resolution mass-spectrometry-based proteomics might be conducive to MPs exploration, especially for low-abundance proteins. In this study, Q-Exactive HF (HF) was used to survey proteins from the same testis tissues separated by two separating methods (tricine- and glycine-SDS-PAGE), as previously described. A total of 8526 proteins were identified, of which more low-abundance proteins were uniquely detected in HF data but not in our previous LTQ Orbitrap Velos (Velos) reanalysis data. Further transcriptomics analysis showed that these uniquely identified proteins by HF also had lower expression at the mRNA level. Of the 81 total identified MPs, 74 and 39 proteins were listed as MPs in HF and Velos data sets, respectively. Among the above MPs, 47 proteins (43 neXtProt PE2 and 4 PE3) were ranked as confirmed MPs after verifying with the stringent spectra match and isobaric and single amino acid variants filtering. Functional investigation of these 47 MPs revealed that 11 MPs were testis-specific proteins and 7 MPs were involved in spermatogenesis process. Therefore, we concluded that higher scanning speed and resolution of HF might be factors for improving the low-abundance MP identification in future C-HPP studies. All mass-spectrometry data from this study have been deposited in the ProteomeXchange with identifier PXD004092.
机译:自2012年以来,通过各种生化策略,缺失蛋白(MPs)研究一直是染色体中心人类蛋白质组计划(C-HPP)的关键任务之一。根据我们先前对睾丸MPs的研究,更快的扫描速度和基于质谱的高分辨率蛋白质组学可能有助于MPs的探索,尤其是对于低丰度蛋白。在这项研究中,如前所述,Q-Exactive HF(HF)用于调查来自通过两种分离方法(三氢精氨酸和甘氨酸-SDS-PAGE)分离的同一睾丸组织的蛋白质。总共鉴定出8526种蛋白质,其中在HF数据中唯一检测到了更多的低丰度蛋白质,但在我们之前的LTQ Orbitrap Velos(Velos)重新分析数据中却没有。进一步的转录组学分析显示,这些通过HF独特鉴定的蛋白质在mRNA水平上也具有较低的表达。在81种已鉴定的MP中,分别在HF和Velos数据集中将74和39种蛋白质列为MP。在上述MP中,经过严格的光谱匹配以及同量异位和单个氨基酸变体过滤后,将47种蛋白质(43个neXtProt PE2和4个PE3)列为确认的MP。对这47个MP的功能研究表明,有11个MP是睾丸特异性蛋白,而7个MP参与了生精过程。因此,我们得出结论,在未来的C-HPP研究中,较高的扫描速度和HF的分辨率可能是改善低丰度MP鉴定的因素。该研究的所有质谱数据均已存储在ProteomeXchange中,标识符为PXD004092。

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