ISOTOPE ASSISTED METABOLOMICS

同位素辅助代谢组学

• 批准号: 7954625
• 负责人: JOHN LUTE MARKLEY
• 金额: $ 1.26万
• 依托单位: UNIVERSITY OF WISCONSIN-MADISON
• 依托单位国家: 美国
• 财政年份: 2009
• 资助国家: 美国
• 起止时间: 2009-03-01 至 2010-02-28
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7954625
• 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的一个 由NIH/NCRR资助的中心赠款提供的资源。子项目和 研究者（PI）可能从另一个NIH来源获得了主要资金， 因此可以在其他CRISP条目中表示。所列机构为 研究中心，而研究中心不一定是研究者所在的机构。 同位素辅助的差异代谢组学：全球代谢谱高通量分析的新策略。 在过去的10年中，大量的努力致力于开发用于分析生物样品中代谢物的高通量方法。 虽然我们可以用质谱法（MS）检测低至10-18摩尔浓度的分子，并可以使用核磁共振（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性能。 我们开发了一种新的基于重同位素的策略，最大限度地减少了与传统方法相关的问题，并扩展了全球代谢谱的范围和再现性。 我们目前正在利用这种方法研究基因敲除拟南芥的抗旱机制，并阐明人类红细胞代谢通量的调控。