1H NMR分析血液代谢物的新限制

IF 2.624
G.A. Nagana Gowda , Vadim Pascua , Daniel Raftery
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引用次数: 3

摘要

人体血液是临床和代谢组学领域应用最广泛的生物标本。虽然质谱法和核磁共振光谱法是代谢组学领域的两个主要分析平台,但核磁共振在血液代谢物分析中表现出几个无与伦比的特征,其中最重要的是其识别未知代谢物的能力及其定量性质。然而,核磁共振可获得的代谢物数量相对较少,限制了其应用范围。因此,提高血液中已鉴定代谢物的限度将极大地影响基于核磁共振的代谢组学。为了继续解决这一重大问题,我们目前的研究描述了12种代谢物的鉴定,这将可量化的血液代谢物的数量扩大了约15%。这些结果与我们早期的努力相结合,现在提供了近90种代谢物,这是迄今为止在代谢组学领域广泛使用的简单1D 1H NMR实验中最高的。利用1D/2D核磁共振技术对人体血液和血浆进行综合研究,鉴定代谢物。新鉴定的代谢物基于化学位移数据库,在与血液/血浆相同的条件下获得的真实化合物的光谱,以及最后使用真实化合物的峰值实验进行验证。考虑到核磁共振的高再现性和化学位移对改变样品条件的敏感性,为新鉴定的代谢物提供了实验方案和峰注释,作为常规应用中鉴定血液代谢物的模板。另外,鉴定的代谢物对分析前条件的敏感性进行了评估。结果表明,在新鉴定的代谢物中,肌苷一磷酸(IMP)和烟酰胺与不稳定辅酶相关,其水平对分析前条件敏感。该研究表明,利用核磁共振将可量化的血液代谢物扩展到一个新的高度,预计将极大地影响血液代谢组学。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A new limit for blood metabolite analysis using 1H NMR spectroscopy

A new limit for blood metabolite analysis using 1H NMR spectroscopy

Human blood is the most widely used biospecimen in the clinic and the metabolomics field. While both mass spectrometry and NMR spectroscopy are the two premier analytical platforms in the metabolomics field, NMR exhibits several unsurpassed characteristics for blood metabolite analysis, the most important of which are its ability to identify unknown metabolites and its quantitative nature. However, the relatively small number of metabolites accessible by NMR has restricted the scope of its applications. Enhancing the limit of identified metabolites in blood will therefore greatly impact NMR-based metabolomics. Continuing our efforts to address this major issue, our current study describes the identification of 12 metabolites, which expands the number of quantifiable blood metabolites by ∼15%. These results, in combination with our earlier efforts, now provide access to nearly 90 metabolites, which is the highest to date for a simple 1D 1H NMR experiment that is widely used in the metabolomics field. Metabolites were identified based on the comprehensive investigation of human blood and plasma using 1D/2D NMR techniques. The newly identified metabolites were validated based on chemical shift databases, spectra of authentic compounds obtained under conditions identical to blood/plasma, and, finally, spiking experiments using authentic compounds. Considering the high reproducibility of NMR and the sensitivity of chemical shifts to altered sample conditions, experimental protocols and peak annotations are provided for the newly identified metabolites, which serve as a template for identification of blood metabolites for routine applications. Separately, the identified metabolites were evaluated for their sensitivity to preanalytical conditions. The results reveal that among the newly identified metabolites, inosine monophosphate (IMP) and nicotinamide are associated with labile coenzymes and their levels are sensitive to preanalytical conditions. The study demonstrates the expansion of quantifiable blood metabolites using NMR to a new height and is expected to greatly impact blood metabolomics.

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