ISOTOPE ASSISTED METABOLOMICS

同位素辅助代谢组学

• 批准号: 8168948
• 负责人: JOHN LUTE MARKLEY
• 金额: $ 0.37万
• 依托单位: UNIVERSITY OF WISCONSIN-MADISON
• 依托单位国家: 美国
• 财政年份: 2010
• 资助国家: 美国
• 起止时间: 2010-03-01 至 2011-02-28
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8168948
• 关键词: Biological; Computer Retrieval of Information on Scientific Projects Database; Droughts; Erythrocytes; Funding; Genetic; Grant; Human; Institution; Isotopes; Knock-out; Mass Spectrum Analysis; Metabolic; Methods; Mouse-ear Cress; Nuclear Magnetic Resonance; Performance; Regulation; Reproducibility; Research; Research Personnel; Resistance; Resources; Sampling; Source; Techniques; United States National Institutes of Health; base; high throughput analysis; metabolomics

This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. Isotope-Assisted Differential Metabolomics: a New Strategy for High Throughput Analysis of Global Metabolic Profiles. Over the past 10 years, a considerable effort has been devoted to developing high throughput methods for profiling metabolites in biological samples. Although we can detect molecules at concentrations as low as 10-18 molar with mass spectrometry (MS) and can differentiate between closely related species using nuclear magnetic resonance (NMR), sample complexity has severely limited the performance of these techniques in metabolomics studies. We have developed a new heavy-isotope based strategy that minimizes problems associated with traditional methods and extends the scope and reproducibility of global metabolic profiling. We are currently using this approach to investigate the mechanism of drought resistant in genetic knockouts of Arabidopsis thaliana and to elucidate the regulation of metabolic flux in human erythrocytes.

这个子项目是许多研究子项目中利用 资源由NIH/NCRR资助的中心拨款提供。子项目和 调查员(PI)可能从NIH的另一个来源获得了主要资金， 并因此可以在其他清晰的条目中表示。列出的机构是 该中心不一定是调查人员的机构。 同位素辅助差异代谢组学：全球代谢谱高通量分析的新策略。在过去的10年里，人们致力于开发高通量的方法来分析生物样品中的代谢物。虽然我们可以用质谱仪(MS)检测浓度低至10-18摩尔的分子，并可以用核磁共振(NMR)区分密切相关的物种，但样品的复杂性严重限制了这些技术在代谢组学研究中的表现。我们开发了一种新的基于重同位素的策略，将与传统方法相关的问题降至最低，并扩大了全球代谢图谱的范围和重复性。我们目前正在使用这种方法来研究拟南芥基因敲除的抗旱机制，并阐明人类红细胞代谢通量的调节。