13C代谢组学:NMR和IROA未知鉴定

Chaevien S. Clendinen, Gregory S. Stupp, Bing Wang, T. Garrett, A. Edison
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引用次数: 12

摘要

摘要:背景同位素比离群分析(IROA)是一种非靶向代谢组学方法,利用稳定同位素标记和LC-HRMS在不同实验条件下对生物样品中的代谢物进行鉴定和相对定量。目的介绍了一种利用高灵敏度13C核磁共振鉴定从IROA LC-HRMS实验中分离出的未知代谢物的方法。方法采用LC-HRMS分离秀丽隐杆线虫IROA样品,5次重复注射,30秒提取。用13C核磁共振对其进行浓缩分析。结果对秀丽隐杆线虫样品进行了同位素标记,并收集到2个相邻的LC部分。通过HRMS,其中一种含有至少2种已知代谢物,苯丙氨酸和肌苷,另一种含有色氨酸和一种未知特征,单同位素质量为m/z 380.0742 [m +H]+。通过核磁共振,我们可以很容易地验证已知的化合物,然后我们确定了导致未知共振的自旋系统网络。在检索BMRB数据库并比较LC-HRMS的分子式后,我们确定这些片段是经过修饰的邻氨基苯甲酸酯和经过磷酸修饰的葡萄糖。然后,我们进行了量子化学核磁共振化学位移计算,以确定最可能的异构体,即3 ' - o-磷酸-β- d -葡萄糖吡喃基-邻氨基甲酸酯。这种化合物之前在同一种生物体中被发现,证实了我们的方法。我们能够重复以前已知的代谢物,并通过与NMR数据库匹配共振并使用化学位移计算来确定正确的同分异构体,从而鉴定出数据库中没有的代谢物。这种方法是有效的,并且可以使用IROA所用的相同材料来识别未知的感兴趣的化合物。
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13C Metabolomics: NMR and IROA for Unknown Identification
Abstract: Background Isotopic Ratio Outlier Analysis (IROA) is an untargeted metabolomics method that uses stable isotopic labeling and LC-HRMS for identification and relative quantification of metabolites in a biological sample under varying experimental conditions. Objective We demonstrate a method using high-sensitivity 13C NMR to identify an unknown metabolite isolated from fractionated material from an IROA LC-HRMS experiment. Methods IROA samples from the nematode Caenorhabditis elegans were fractionated using LC-HRMS using 5 repeated injections and collecting 30 sec fractions. These were concentrated and analyzed by 13C NMR. Results We isotopically labeled samples of C. elegans and collected 2 adjacent LC fractions. By HRMS, one contained at least 2 known metabolites, phenylalanine and inosine, and the other contained tryptophan and an unknown feature with a monoisotopic mass of m/z 380.0742 [M+H]+. With NMR, we were able to easily verify the known compounds, and we then identified the spin system networks responsible for the unknown resonances. After searching the BMRB database and comparing the molecular formula from LC-HRMS, we determined that the fragments were a modified anthranilate and a glucose modified by a phosphate. We then performed quantum chemical NMR chemical shift calculations to determine the most likely isomer, which was 3’-O-phospho-β-D-glucopyranosyl-anthranilate. This compound had previously been found in the same organism, validating our approach. Conclusion We were able to dereplicate previously known metabolites and identify a metabolite that was not in databases by matching resonances to NMR databases and using chemical shift calculations to determine the correct isomer. This approach is efficient and can be used to identify unknown compounds of interest using the same material used for IROA.
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