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A workflow to increase the detection rate of proteins from unsequenced organisms in high-throughput proteomics experiments

机译:在高通量蛋白质组学实验中提高未测序生物蛋白质检测率的工作流程

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摘要

We present and evaluate a strategy for the mass spectrometric identification of proteins from organisms for which no genome sequence information is available that incorporates cross-species information from sequenced organisms. The presented method combines spectrum quality scoring, de novo sequencing and error tolerant BLAST searches and is designed to decrease input data complexity. Spectral quality scoring reduces the number of investigated mass spectra without a loss of information. Stringent quality-based selection and the combination of different de novo sequencing methods substantially increase the catalog of significant peptide alignments. The de novo sequences passing a reliability filter are subsequently submitted to error tolerant BLAST searches and MS-BLAST hits are validated by a sampling technique. With the described workflow, we identified up to 20% more groups of homologous proteins in proteome analyses with organisms whose genome is not sequenced than by state-of-the-art database searches in an Arabidopsis thaliana database. We consider the novel data analysis workflow an excellent screening method to identify those proteins that evade detection in proteomics experiments as a result of database constraints.
机译:我们提出并评估一种从生物中进行蛋白质质谱鉴定的策略,对于该策略而言,没有可用于基因组序列信息的生物,其中该基因组信息不包含已测序生物的跨物种信息。提出的方法结合了频谱质量评分,从头排序和容错BLAST搜索,旨在降低输入数据的复杂性。光谱质量评分可减少所研究质谱的数量,而不会丢失信息。严格的基于质量的选择以及不同的从头测序方法的组合大大增加了重要肽段比对的目录。随后将通过可靠性过滤器的从头序列进行容错BLAST搜索,并通过采样技术验证MS-BLAST命中。通过所描述的工作流程,与通过拟南芥数据库进行的最新数据库搜索相比,在蛋白质组分析中,其基因组未测序的生物最多可识别出多达20%的同源蛋白质组。我们认为新颖的数据分析工作流程是一种出色的筛选方法,可以识别由于数据库限制而在蛋白质组学实验中逃避检测的那些蛋白质。

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