宏蛋白质组学的肽丰度相关性增强了人类肠道微生物组的分类和功能分析。

IF 9.2 1区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Zhongzhi Sun, Zhibin Ning, Qing Wu, Leyuan Li, Andrew C Doxey, Daniel Figeys
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引用次数: 0

摘要

基于质谱(MS)的蛋白质组学广泛应用于定量蛋白质分析和蛋白质相互作用研究。然而,目前大多数研究都集中在单物种蛋白质组学上,而由数百种细菌组成的复杂微生物组中的蛋白质相互作用在很大程度上仍未被探索。在这项研究中,我们分析了宏蛋白质组学数据集中肽丰度的相关性,该数据集来自体外培养的受各种药物治疗的人肠道微生物组。我们的分析表明,来自同一蛋白质或分类单元的肽表现出相关的丰度变化。通过使用t-SNE进行可视化,我们生成了一个肽相关图,其中来自同一分类单元的肽形成不同的簇。此外,多肽丰度相关性使更多多肽的基因组水平分类分配成为可能。例如,最初只分配给拟杆菌科的3845个肽中的1880个(48.9%)现在可以分配给特定的基因组。在具有代表性的物种基因组亚群中,基于分类单元归一化肽丰度(TNPA)的肽相关网络连接了功能相关肽,并提供了对未表征蛋白的见解。总之,我们的研究表明,分析肽丰度相关性可以增强人类肠道bb0研究的分类和功能分析。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Peptide abundance correlations in metaproteomics enhance taxonomic and functional analysis of the human gut microbiome.

Mass spectrometry (MS)-based proteomics is widely used for quantitative protein profiling and protein interaction studies. However, most current research focuses on single-species proteomics, while protein interactions within complex microbiomes, composed of hundreds of bacterial species, remain largely unexplored. In this study, we analyzed peptide abundance correlations within a metaproteomics dataset derived from in vitro cultured human gut microbiomes subjected to various drug treatments. Our analysis revealed that peptides from the same protein or taxon exhibited correlated abundance changes. By using t-SNE for visualization, we generated a peptide correlation map in which peptides from the same taxon formed distinct clusters. Furthermore, peptide abundance correlations enabled genome-level taxonomic assignments for a greater number of peptides. For instance, 1880 (48.9%) of the 3845 peptides initially assigned only to the family Bacteroidaceae could now be assigned to a specific genome. In species representative genome subsets, peptide correlation networks based on taxon-normalized peptide abundance (TNPA) linked functionally related peptides and provided insights into uncharacterized proteins. Altogether, our study demonstrates that analyzing peptide abundance correlations enhances both taxonomic and functional analyses in human gut metaproteomics research.

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来源期刊
npj Biofilms and Microbiomes
npj Biofilms and Microbiomes Immunology and Microbiology-Microbiology
CiteScore
12.10
自引率
3.30%
发文量
91
审稿时长
9 weeks
期刊介绍: npj Biofilms and Microbiomes is a comprehensive platform that promotes research on biofilms and microbiomes across various scientific disciplines. The journal facilitates cross-disciplinary discussions to enhance our understanding of the biology, ecology, and communal functions of biofilms, populations, and communities. It also focuses on applications in the medical, environmental, and engineering domains. The scope of the journal encompasses all aspects of the field, ranging from cell-cell communication and single cell interactions to the microbiomes of humans, animals, plants, and natural and built environments. The journal also welcomes research on the virome, phageome, mycome, and fungome. It publishes both applied science and theoretical work. As an open access and interdisciplinary journal, its primary goal is to publish significant scientific advancements in microbial biofilms and microbiomes. The journal enables discussions that span multiple disciplines and contributes to our understanding of the social behavior of microbial biofilm populations and communities, and their impact on life, human health, and the environment.
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