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泛素组学揭示了与人类疾病相关的新网络和关联。

Ubiquitin - omics reveals novel networks and associations with human disease.

机构信息

Henry Wellcome Building for Molecular Physiology, Nuffield Department of Medicine, Roosevelt Drive, University of Oxford, OX3 7BN, UK.

出版信息

Curr Opin Chem Biol. 2013 Feb;17(1):59-65. doi: 10.1016/j.cbpa.2012.12.024. Epub 2013 Jan 19.

Abstract

Human neurodegenerative and infectious diseases and tumorigenesis are associated with alterations in ubiquitin pathways. Over 10% of the genome encode for genes that either bind or manipulate ubiquitin to affect a large proportion of biological processes. This has been the basis for the development of approaches allowing the enrichment of ubiquitinated proteins for comparisons using proteomics and mass spectrometry. Tools such as tagged tandem ubiquitin binding domains, chemically derivatized ubiquitin or anti-gly-gly-lys antibodies combined with mass spectrometry have contributed to surveys of poly-ubiquitinated proteins, poly-ubiquitin linkage diversity and protein ubiquitination sites and their relation to other posttranslational modifications at a proteome wide level, providing insights in to how dynamic alterations in ubiquitination and deubiquitination steps are associated with normal physiology and pathogenesis.

摘要

人类神经退行性疾病、传染病和肿瘤的发生与泛素途径的改变有关。超过 10%的基因组编码的基因可以结合或修饰泛素,从而影响大部分的生物学过程。这为发展允许富集泛素化蛋白质的方法提供了基础,这些方法可以使用蛋白质组学和质谱进行比较。标记串联泛素结合结构域、化学衍生化泛素或抗甘氨酰-甘氨酸-赖氨酸抗体与质谱相结合,有助于对多泛素化蛋白质、多泛素连接多样性以及蛋白质泛素化位点及其与其他翻译后修饰的关系进行调查,从而深入了解泛素化和去泛素化步骤的动态变化如何与正常生理和发病机制相关。

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