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基于计算蛋白质组学工作流程鉴定由小开放阅读框编码的新型细菌微蛋白。

Identification of Novel Bacterial Microproteins Encoded by Small Open Reading Frames Using a Computational Proteogenomics Workflow.

机构信息

Centro de Pesquisas em Biologia Molecular e Funcional (CPBMF) and Instituto Nacional de Ciência e Tecnologia em Tuberculose (INCT-TB), Pontifícia Universidade Católica do Rio Grande do Sul (PUCRS), Porto Alegre, Brazil.

Programa de Pós-Graduação em Biologia Celular e Molecular, Pontifícia Universidade Católica do Rio Grande do Sul, Porto Alegre, Rio Grande do Sul, Brazil.

出版信息

Methods Mol Biol. 2024;2836:19-34. doi: 10.1007/978-1-0716-4007-4_2.

Abstract

Genome annotation has historically ignored small open reading frames (smORFs), which encode a class of proteins shorter than 100 amino acids, collectively referred to as microproteins. This cutoff was established to avoid thousands of false positives due to limitations of pure genomics pipelines. Proteogenomics, a computational approach that combines genomics, transcriptomics, and proteomics, makes it possible to accurately identify these short sequences by overlaying different levels of omics evidence. In this chapter, we showcase the use of μProteInS, a bioinformatics pipeline developed for the identification of unannotated microproteins encoded by smORFs in bacteria. The workflow covers all the steps from quality control and transcriptome assembly to the scoring and post-processing of mass spectrometry data. Additionally, we provide an example on how to apply the pipeline's machine learning method to identify high-confidence spectra and pinpoint the most reliable identifications from large datasets.

摘要

基因组注释在历史上忽略了小开放阅读框 (smORFs),这些小开放阅读框编码一类长度小于 100 个氨基酸的蛋白质,统称为微蛋白。这一截止值是为了避免由于纯基因组学管道的限制而产生数千个假阳性结果。蛋白质组学是一种将基因组学、转录组学和蛋白质组学相结合的计算方法,通过覆盖不同层次的组学证据,使得准确识别这些短序列成为可能。在本章中,我们展示了 μProteInS 的使用,μProteInS 是一种生物信息学管道,用于识别细菌中由 smORFs 编码的未注释的微蛋白。该工作流程涵盖了从质量控制和转录组组装到质谱数据评分和后处理的所有步骤。此外,我们还提供了一个示例,说明如何应用该管道的机器学习方法来识别高可信度的光谱,并从大型数据集精确定位最可靠的鉴定。

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