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解析小鼠免疫器官的核酸结合蛋白质组揭示衰老的关键蛋白

Deciphering Nucleic Acid Binding Proteome of Mouse Immune Organs Reveals Hub Proteins for Aging.

机构信息

State Key Laboratory of Microbial Metabolism, Joint International Research Laboratory of Metabolic & Developmental Sciences, School of Life Sciences and Biotechnology, Shanghai Jiao Tong University, Shanghai, China.

School of Pharmacy, Shanghai Jiao Tong University, Shanghai, China.

出版信息

Mol Cell Proteomics. 2023 Aug;22(8):100611. doi: 10.1016/j.mcpro.2023.100611. Epub 2023 Jun 28.

Abstract

Profiling the nucleic acid-binding proteins (NABPs) during aging process is critical to elucidate its roles in biological systems as well as transcriptional and translational regulation. Here, we developed a comprehensive strategy to survey the NABPs of mouse immune organs by using single cell preparation and selective capture technology-based proteomics. Our approach provided a global view of tissue NABPs from different organs under normal physiological conditions with extraction specificity of 70 to 90%. Through quantitative proteomics analysis of mouse spleen and thymus at 1, 4, 12, 24, 48, and 72 weeks, we investigated the molecular features of aging-related NABPs. A total of 2674 proteins were quantified in all six stages, demonstrating distinct and time-specific expression pattern of NABPs. Thymus and spleen exhibited unique aging signatures, and differential proteins and pathways were enriched across the mouse lifespan. Three core modules and 16 hub proteins associated with aging were revealed through weighted gene correlation network analysis. Significant candidates were screened for immunoassay verification, and six hub proteins were confirmed. The integrated strategy pertains the capability to decipher the dynamic functions of NABPs in aging physiology and benefit further mechanism research.

摘要

在衰老过程中对核酸结合蛋白(NABPs)进行分析对于阐明其在生物系统中的作用以及转录和翻译调控至关重要。在这里,我们开发了一种综合策略,通过使用单细胞制备和基于选择性捕获技术的蛋白质组学来检测小鼠免疫器官中的 NABPs。我们的方法提供了在正常生理条件下来自不同器官的组织 NABPs 的全局视图,提取特异性为 70%至 90%。通过对 1、4、12、24、48 和 72 周龄的小鼠脾脏和胸腺进行定量蛋白质组学分析,我们研究了与衰老相关的 NABPs 的分子特征。在所有六个阶段共定量了 2674 种蛋白质,证明了 NABPs 的独特且具有时间特异性的表达模式。胸腺和脾脏表现出独特的衰老特征,并且在整个小鼠寿命中差异蛋白和途径被富集。通过加权基因相关网络分析揭示了三个与衰老相关的核心模块和 16 个枢纽蛋白。通过免疫测定验证进行了显著候选物的筛选,并确认了六个枢纽蛋白。该综合策略能够解析 NABPs 在衰老生理中的动态功能,并有助于进一步的机制研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/906a/10412848/10360f564f43/ga1.jpg

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