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用于可靠磷酸化位点定位的替代串联质谱(MS/MS)和生物信息学方法的比较。

Comparison of alternative MS/MS and bioinformatics approaches for confident phosphorylation site localization.

作者信息

Wiese Heike, Kuhlmann Katja, Wiese Sebastian, Stoepel Nadine S, Pawlas Magdalena, Meyer Helmut E, Stephan Christian, Eisenacher Martin, Drepper Friedel, Warscheid Bettina

机构信息

Faculty of Biology, Functional Proteomics, University of Freiburg , 79104 Freiburg, Germany.

出版信息

J Proteome Res. 2014 Feb 7;13(2):1128-37. doi: 10.1021/pr400402s. Epub 2014 Jan 3.

Abstract

Over the past years, phosphoproteomics has advanced to a prime tool in signaling research. Since then, an enormous amount of information about in vivo protein phosphorylation events has been collected providing a treasure trove for gaining a better understanding of the molecular processes involved in cell signaling. Yet, we still face the problem of how to achieve correct modification site localization. Here we use alternative fragmentation and different bioinformatics approaches for the identification and confident localization of phosphorylation sites. Phosphopeptide-enriched fractions were analyzed by multistage activation, collision-induced dissociation and electron transfer dissociation (ETD), yielding complementary phosphopeptide identifications. We further found that MASCOT, OMSSA and Andromeda each identified a distinct set of phosphopeptides allowing the number of site assignments to be increased. The postsearch engine SLoMo provided confident phosphorylation site localization, whereas different versions of PTM-Score integrated in MaxQuant differed in performance. Based on high-resolution ETD and higher collisional dissociation (HCD) data sets from a large synthetic peptide and phosphopeptide reference library reported by Marx et al. [Nat. Biotechnol. 2013, 31 (6), 557-564], we show that an Andromeda/PTM-Score probability of 1 is required to provide an false localization rate (FLR) of 1% for HCD data, while 0.55 is sufficient for high-resolution ETD spectra. Additional analyses of HCD data demonstrated that for phosphotyrosine peptides and phosphopeptides containing two potential phosphorylation sites, PTM-Score probability cutoff values of <1 can be applied to ensure an FLR of 1%. Proper adjustment of localization probability cutoffs allowed us to significantly increase the number of confident sites with an FLR of <1%.Our findings underscore the need for the systematic assessment of FLRs for different score values to report confident modification site localization.

摘要

在过去几年中,磷酸化蛋白质组学已发展成为信号研究中的一项重要工具。从那时起,关于体内蛋白质磷酸化事件的大量信息被收集起来,为更好地理解细胞信号传导中涉及的分子过程提供了一个宝库。然而,我们仍然面临着如何实现正确的修饰位点定位的问题。在这里,我们使用替代碎裂和不同的生物信息学方法来鉴定和可靠地定位磷酸化位点。通过多级激活、碰撞诱导解离和电子转移解离(ETD)对富含磷酸肽的组分进行分析,产生互补的磷酸肽鉴定结果。我们进一步发现,MASCOT、OMSSA和Andromeda各自鉴定出一组不同的磷酸肽,从而增加了位点分配的数量。搜索后引擎SLoMo提供了可靠的磷酸化位点定位,而整合在MaxQuant中的不同版本的PTM-Score在性能上有所不同。基于马克思等人[《自然生物技术》2013年,31(6),557 - 564]报道的来自大型合成肽和磷酸肽参考文库的高分辨率ETD和更高碰撞解离(HCD)数据集,我们表明,对于HCD数据,要提供1%的错误定位率(FLR),Andromeda/PTM-Score概率需为1,而对于高分辨率ETD光谱,0.55就足够了。对HCD数据的进一步分析表明,对于磷酸酪氨酸肽和含有两个潜在磷酸化位点的磷酸肽,PTM-Score概率截止值<1可用于确保1%的FLR。对定位概率截止值的适当调整使我们能够显著增加FLR<1%的可靠位点数量。我们的研究结果强调了对不同得分值的FLR进行系统评估以报告可靠修饰位点定位的必要性。

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