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本文引用的文献

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A Western diet induced NAFLD in LDLR(-/)(-) mice is associated with reduced hepatic glutathione synthesis.西方饮食诱导低密度脂蛋白受体基因敲除(LDLR(-/-))小鼠发生非酒精性脂肪性肝病(NAFLD),这与肝脏谷胱甘肽合成减少有关。
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Circulating protein synthesis rates reveal skeletal muscle proteome dynamics.循环蛋白合成速率揭示骨骼肌蛋白质组动态变化。
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Natural isotope correction of MS/MS measurements for metabolomics and (13)C fluxomics.代谢组学和(13)C通量组学中MS/MS测量的天然同位素校正
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Monitoring newly synthesized proteins over the adult life span of Caenorhabditis elegans.在秀丽隐杆线虫的整个成年生命周期中监测新合成的蛋白质。
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Protein kinetic signatures of the remodeling heart following isoproterenol stimulation.异丙肾上腺素刺激后重塑心脏的蛋白质动力学特征。
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使用质谱法监测生物分子的合成。

Monitoring the synthesis of biomolecules using mass spectrometry.

作者信息

Miyagi Masaru, Kasumov Takhar

机构信息

Center for Proteomics and Bioinformatics, Department of Nutrition, Case Western Reserve University, Cleveland, OH 44106, USA

Mass Spectrometry Laboratory, Department of Pharmaceutical Sciences, Northeast Ohio Medical University, Rootstown, OH 44272, USA.

出版信息

Philos Trans A Math Phys Eng Sci. 2016 Oct 28;374(2079). doi: 10.1098/rsta.2015.0378.

DOI:10.1098/rsta.2015.0378
PMID:27644976
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5031643/
Abstract

The controlled and selective synthesis/clearance of biomolecules is critical for most cellular processes. In most high-throughput 'omics' studies, we measure the static quantities of only one class of biomolecules (e.g. DNA, mRNA, proteins or metabolites). It is, however, important to recognize that biological systems are highly dynamic in which biomolecules are continuously renewed and different classes of biomolecules interact and affect each other's production/clearance. Therefore, it is necessary to measure the turnover of diverse classes of biomolecules to understand the dynamic nature of biological systems. Herein, we explain why the kinetic analysis of a diverse range of biomolecules is important and how such an analysis can be done. We argue that heavy water ((2)H2O) could be a universal tracer for monitoring the synthesis of biomolecules on a global scale.This article is part of the themed issue 'Quantitative mass spectrometry'.

摘要

生物分子的可控和选择性合成/清除对于大多数细胞过程至关重要。在大多数高通量“组学”研究中,我们仅测量一类生物分子(例如DNA、mRNA、蛋白质或代谢物)的静态量。然而,必须认识到生物系统是高度动态的,其中生物分子不断更新,不同类别的生物分子相互作用并影响彼此的产生/清除。因此,有必要测量不同类别的生物分子的周转率,以了解生物系统的动态性质。在此,我们解释了为什么对多种生物分子进行动力学分析很重要以及如何进行这种分析。我们认为重水((2)H2O)可能是用于在全球范围内监测生物分子合成的通用示踪剂。本文是主题为“定量质谱”的特刊的一部分。