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利用蛋白质组学数据挖掘技术绘制阿尔茨海默病脑区的翻译后修饰图谱

Mapping Post-Translational Modifications in Brain Regions in Alzheimer's Disease Using Proteomics Data Mining.

作者信息

Deolankar Sayali Chandrashekhar, Patil Arun H, Rex Devasahayam Arokia Balaya, Subba Pratigya, Mahadevan Anita, Prasad Thottethodi Subrahmanya Keshava

机构信息

Center for Systems Biology and Molecular Medicine, Yenepoya Research Centre, Yenepoya (Deemed to be University), Mangalore, India.

Department of Neuropathology, National Institute of Mental Health and Neurosciences, Bangalore, India.

出版信息

OMICS. 2021 Aug;25(8):525-536. doi: 10.1089/omi.2021.0054. Epub 2021 Jul 13.

Abstract

Alzheimer's disease (AD) is a leading cause of dementia and a neurodegenerative disease. Proteomics and post-translational modification (PTM) analyses offer new opportunities for a comprehensive understanding of pathophysiology of brain in AD. We report here multiple PTMs in patients with AD, harnessing publicly available proteomics data from nine brain regions and at three different Braak stages of disease progression. Specifically, we identified 7190 peptides with PTMs, corresponding to 2545 proteins from brain regions with intermediate tangles, and 6864 peptides with PTMs corresponding to 2465 proteins from brain regions with severe tangles. A total of 103 proteins with PTMs were expressed uniquely to intermediate tangles and severe tangles compared to no tangles. Kyoto Encyclopedia of Genes and Genomes pathway enrichment analysis suggested the association of these proteins in AD progression through platelet activation. These modified proteins were also found to be enriched for the tricarboxylic acid (TCA) cycle, respiratory electron cycle, and detoxification of reactive oxygen species. The multi-PTM data reported here contribute to our understanding of the neurobiology of AD and highlight the prospects of omics systems science research in neurodegenerative diseases. The present study provides a region-wise classification for the proteins with PTMs along with their differential expression patterns, providing insights into the localization of these proteins upon modification. The catalog of multi-PTMs identified in the context of AD from different brain regions provides a unique platform for generating newer hypotheses in understanding the putative role of specific PTMs in AD pathogenesis.

摘要

阿尔茨海默病(AD)是痴呆症的主要病因,也是一种神经退行性疾病。蛋白质组学和翻译后修饰(PTM)分析为全面了解AD患者大脑的病理生理学提供了新的机会。我们利用来自九个脑区和疾病进展的三个不同Braak阶段的公开蛋白质组学数据,报告了AD患者的多种PTM。具体而言,我们鉴定出7190个具有PTM的肽段,对应于来自有中度缠结脑区的2545种蛋白质,以及6864个具有PTM的肽段,对应于来自有重度缠结脑区的2465种蛋白质。与无缠结相比,共有103种具有PTM的蛋白质在中度缠结和重度缠结中独特表达。京都基因与基因组百科全书通路富集分析表明,这些蛋白质通过血小板激活与AD进展相关。还发现这些修饰蛋白在三羧酸(TCA)循环、呼吸电子循环和活性氧解毒方面富集。本文报道的多PTM数据有助于我们理解AD的神经生物学,并突出了组学系统科学研究在神经退行性疾病中的前景。本研究提供了具有PTM的蛋白质的区域分类及其差异表达模式,为这些蛋白质修饰后的定位提供了见解。在AD背景下从不同脑区鉴定出的多PTM目录为理解特定PTM在AD发病机制中的假定作用产生新假设提供了一个独特的平台。

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