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PROTEOFORMER 2.0: Further Developments in the Ribosome Profiling-assisted Proteogenomic Hunt for New Proteoforms

机译:Proteoformer 2.0:用于新蛋白质ord的核糖体剖面辅助蛋白叶蛋白酶的进一步发展

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PROTEOFORMER is a pipeline that enables the automated processing of data derived from ribosome profiling (RIBO-seq, i. e. the sequencing of ribosome-protected mRNA fragments). As such, genome-wide ribosome occupancies lead to the delineation of data-specific translation product candidates and these can improve the mass spectrometry-based identification. Since its first publication, different upgrades, new features and extensions have been added to the PROTEOFORMER pipeline. Some of the most important upgrades include P-site offset calculation during mapping, comprehensive data preexploration, the introduction of two alternative proteoform calling strategies and extended pipeline output features. These novelties are illustrated by analyzing ribosome profiling data of human HCT116 and Jurkat data. The different proteoform calling strategies are used alongside one another and in the end combined together with reference sequences from UniProt. Matching mass spectrometry data are searched against this extended search space with MaxQuant. Overall, besides annotated proteoforms, this pipeline leads to the identification and validation of different categories of new proteoforms, including translation products of up-and downstream open reading frames, 5 and 3 extended and truncated proteoforms, single amino acid variants, splice variants and translation products of so-called noncoding regions. Further, proof-of-concept is reported for the improvement of spectrum matching by including Prosit, a deep neural network strategy that adds extra fragmentation spectrum intensity features to the analysis. In the light of ribosome profiling-driven proteogenomics, it is shown that this allows validating the spectrum matches of newly identified proteoforms with elevated stringency. These updates and novel conclusions provide new insights and lessons for the ribosome profiling-based proteogenomic research field. More practical information on the pipeline, raw code, the user manual (README) and explanations on the different modes of availability can be found at the GitHub repository of PROTEOFORMER: https://github. com/ Biobix/proteoformer.
机译:蛋白质order是一种管道,它能够自动处理来自核糖体分析的数据(Ribo-Seq,I.e。核糖体保护的mRNA片段的测序)。因此,基因组核糖体占据导致数据特异性翻译产品候选者的描绘,这些核糖剂可以改善基于质谱的鉴定。自从其第一次出版物以来,植物管道中已添加不同的升级,新功能和扩展。一些最重要的升级包括在映射期间的P-Site偏移量计算,综合数据预先绘制,引入了两种替代的蛋白质调用策略和扩展流水线输出功能。通过分析人HCT116和Jurkat数据的核糖体分析数据来说明这些Noveltizes。不同的蛋白质呼唤策略彼此旁边和末端一起使用,与Uniprot的参考序列组合在一起。匹配质谱数据被搜索,并以MaxQuant搜索此扩展搜索空间。总体而言,除了带注释的蛋白质形状之外,该管道也能够识别和验证不同类别的新型蛋白质常规,包括翻译产品的上下开放阅读框架,5和3延伸和截断的蛋白质ort,单氨基酸变体,剪接变体和翻译所谓的非编码区的产品。此外,据报道,通过包括价格的深度神经网络策略来提高概念验证,该策略为分析增加了额外的碎片谱强度特征。鉴于核糖体的分析驱动的蛋白质组织,表明这允许通过升高的严格性验证新鉴定的蛋白质常规的谱比匹配。这些更新和新的结论为核糖体仿形的突源性研究领域提供了新的见解和课程。在Proteoformer的GitHub存储库中找到有关管道,原始代码,用户手册(README)和关于不同可用模式的解释的更实用信息,可以在PROFEOFORMER:https:// github中找到。 com / biobix / proteoformer。

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