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代谢组学方法全面分析不同结构域中的氨基酸。

Metabolomics method to comprehensively analyze amino acids in different domains.

作者信息

Gu Haiwei, Du Jianhai, Carnevale Neto Fausto, Carroll Patrick A, Turner Sally J, Chiorean E Gabriela, Eisenman Robert N, Raftery Daniel

机构信息

Northwest Metabolomics Research Center, Department of Anesthesiology and Pain Medicine, University of Washington, 850 Republican St., Seattle, WA 98109, USA.

出版信息

Analyst. 2015 Apr 21;140(8):2726-34. doi: 10.1039/c4an02386b. Epub 2015 Feb 20.

Abstract

Amino acids play essential roles in both metabolism and the proteome. Many studies have profiled free amino acids (FAAs) or proteins; however, few have connected the measurement of FAA with individual amino acids in the proteome. In this study, we developed a metabolomics method to comprehensively analyze amino acids in different domains, using two examples of different sample types and disease models. We first examined the responses of FAAs and insoluble-proteome amino acids (IPAAs) to the Myc oncogene in Tet21N human neuroblastoma cells. The metabolic and proteomic amino acid profiles were quite different, even under the same Myc condition, and their combination provided a better understanding of the biological status. In addition, amino acids were measured in 3 domains (FAAs, free and soluble-proteome amino acids (FSPAAs), and IPAAs) to study changes in serum amino acid profiles related to colon cancer. A penalized logistic regression model based on the amino acids from the three domains had better sensitivity and specificity than that from each individual domain. To the best of our knowledge, this is the first study to perform a combined analysis of amino acids in different domains, and indicates the useful biological information available from a metabolomics analysis of the protein pellet. This study lays the foundation for further quantitative tracking of the distribution of amino acids in different domains, with opportunities for better diagnosis and mechanistic studies of various diseases.

摘要

氨基酸在新陈代谢和蛋白质组中都起着至关重要的作用。许多研究已对游离氨基酸(FAA)或蛋白质进行了分析;然而,很少有研究将FAA的测量与蛋白质组中的单个氨基酸联系起来。在本研究中,我们开发了一种代谢组学方法,以两个不同样本类型和疾病模型的例子,全面分析不同区域的氨基酸。我们首先研究了Tet21N人神经母细胞瘤细胞中FAA和不溶性蛋白质组氨基酸(IPAA)对Myc癌基因的反应。即使在相同的Myc条件下,代谢和蛋白质组氨基酸谱也有很大差异,它们的组合能更好地了解生物学状态。此外,我们在三个区域(FAA、游离和可溶性蛋白质组氨基酸(FSPAA)以及IPAA)中测量氨基酸,以研究与结肠癌相关的血清氨基酸谱变化。基于这三个区域氨基酸的惩罚逻辑回归模型比每个单独区域的模型具有更好的敏感性和特异性。据我们所知,这是首次对不同区域的氨基酸进行联合分析的研究,表明从蛋白质沉淀的代谢组学分析中可获得有用的生物学信息。本研究为进一步定量追踪氨基酸在不同区域的分布奠定了基础,为各种疾病的更好诊断和机制研究提供了机会。

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