Peptidomics: A New Dimension in Microbiome Research.

IF 2.5 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Kai Hilpert
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引用次数: 0

Abstract

The human gut microbiome is now recognised as a major determinant of health, with roles extending beyond digestion to influence neurodegeneration, metabolism, immunity, and pharmacological responses. Clinical studies link microbial imbalances to Alzheimer's disease, Parkinson's disease, depression, and cardiovascular disorders, yet the underlying mechanisms remain only partly understood. Methodological advances have progressively deepened our insight. DNA-based sequencing (metagenomics) catalogues microbial genes but reveals only potential functions. RNA-based sequencing (metatranscriptomics) highlights active gene expression, but instability of transcripts and poor correlation with protein activity limit its predictive value. Metabolomics measures small-molecule end products, providing direct evidence of microbial biochemistry and identifying disease-linked metabolites such as urolithin A, trimethylamine N-oxide, and equol. These approaches together have transformed microbiome science, but they remain incomplete. A critical and underutilised dimension is peptidomics: the systematic analysis of endogenous peptides in the gut and circulation. Enabled by peptide-enriching, protease-inhibiting workflows and high-resolution liquid chromatography-tandem mass spectrometry (LC-MS/MS), peptidomics directly captures unstable signaling peptides and proteolytic fragments that are often invisible to conventional proteomics. Coupled with emerging gut-specific peptide databases, such as MetaPep, and Artificial Intelligence (AI) assisted de novo sequencing and spectral prediction for non-human peptides, this provides a concrete technical route to reading out the functional peptide layer of the microbiome. Peptidomics can capture functional signals of host-microbiome interaction, reveal context-specific biomarkers, and provide mechanistic insight into disease. Recent studies demonstrate that peptide-level resolution uncovers microbial contributions to gut inflammation, modulates the gut-brain axis, and enables peptide-based disease stratification in conditions such as inflammatory bowel disease. However, despite these promising examples, peptidomics remains largely absent from mainstream microbiome research. Integrating peptidomics with existing genomic, transcriptomic, and metabolomic approaches will generate a more complete and functional picture of the microbiome. This shift will accelerate biomarker discovery, refine diagnostics, and expand the search for peptide-based therapeutics, positioning peptidomics as an essential next step in microbiome science.

肽组学:微生物组研究的新方向。
人类肠道微生物群现在被认为是健康的主要决定因素,其作用不仅限于消化,还影响神经变性、代谢、免疫和药理反应。临床研究将微生物失衡与阿尔茨海默病、帕金森病、抑郁症和心血管疾病联系起来,但其潜在机制仅部分被了解。方法论的进步逐渐加深了我们的洞察力。基于dna的测序(宏基因组学)对微生物基因进行了分类,但只揭示了潜在的功能。基于rna的测序(亚转录组学)强调了活跃的基因表达,但转录物的不稳定性和与蛋白质活性的低相关性限制了其预测价值。代谢组学测量小分子最终产物,提供微生物生物化学的直接证据,并确定与疾病相关的代谢物,如尿素A、三甲胺n -氧化物和马雌酚。这些方法共同改变了微生物组科学,但它们仍然不完整。一个关键的和未充分利用的维度是肽组学:对肠道和循环中的内源性肽的系统分析。通过多肽富集、蛋白酶抑制工作流程和高分辨率液相色谱-串联质谱(LC-MS/MS),多肽组学可以直接捕获常规蛋白质组学通常看不见的不稳定信号肽和蛋白水解片段。结合新兴的肠道特异性肽数据库,如MetaPep,以及人工智能(AI)辅助的非人类肽从头测序和光谱预测,这为读取微生物组的功能肽层提供了具体的技术途径。肽组学可以捕获宿主-微生物相互作用的功能信号,揭示特定环境的生物标志物,并提供疾病的机制洞察。最近的研究表明,肽水平的分辨率揭示了微生物对肠道炎症的贡献,调节肠-脑轴,并使炎症性肠病等疾病的基于肽的疾病分层成为可能。然而,尽管有这些有希望的例子,肽组学在主流微生物组研究中仍然很大程度上缺席,这需要改变。将肽组学与现有的基因组学、转录组学和代谢组学方法相结合,将产生更完整的微生物组功能图谱。这一转变将加速生物标志物的发现,改进诊断,扩大对基于肽的治疗方法的研究,将肽组学定位为微生物组科学的重要下一步。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Protein and Peptide Letters
Protein and Peptide Letters 生物-生化与分子生物学
CiteScore
2.90
自引率
0.00%
发文量
98
审稿时长
2 months
期刊介绍: Protein & Peptide Letters publishes letters, original research papers, mini-reviews and guest edited issues in all important aspects of protein and peptide research, including structural studies, advances in recombinant expression, function, synthesis, enzymology, immunology, molecular modeling, and drug design. Manuscripts must have a significant element of novelty, timeliness and urgency that merit rapid publication. Reports of crystallization and preliminary structure determination of biologically important proteins are considered only if they include significant new approaches or deal with proteins of immediate importance, and preliminary structure determinations of biologically important proteins. Purely theoretical/review papers should provide new insight into the principles of protein/peptide structure and function. Manuscripts describing computational work should include some experimental data to provide confirmation of the results of calculations. Protein & Peptide Letters focuses on: Structure Studies Advances in Recombinant Expression Drug Design Chemical Synthesis Function Pharmacology Enzymology Conformational Analysis Immunology Biotechnology Protein Engineering Protein Folding Sequencing Molecular Recognition Purification and Analysis
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