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Matrix-assisted laser desorption/ionization matrices for negative mode metabolomics

机译:负模代谢组学的基质辅助激光解吸/电离矩阵

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摘要

Matrix-assisted laser desorption/ionization (MALDI) has been shown to be highly sensitive for analyzing low-mass compounds such as metabolites if the right matrix is used. 9-aminoacridine (9AA) is the most commonly employed matrix for negative mode MALDI-MS in metabolomics. However, matrix interferences and the strongly varying sensitivity for different metabolites make a search for alternative matrices desirable, in order to identify compounds with a different chemical background and/or favoring a different range of analytes. We tested the performance of a series of potential negative mode MALDI matrices with a mix of 29 metabolites containing amino acids, nucleotide phosphates and Krebs cycle intermediates. While ethacridine lactate was found to provide limits of detection (LODs) in the low femtomole range for nucleotide phosphates, amino acids and Krebs cycle intermediates in the low picomole range, 4-amino-2-methylquinoline showed LODs in the picomole range for most metabolites, but is capable of ionizing a broader range of analytes than both 9AA and ethacridine.
机译:如果使用正确的基质,基质辅助激光解吸/电离(MALDI)已显示出对分析低质量化合物(例如代谢产物)非常敏感。 9-氨基ac啶(9AA)是代谢组学中阴性模式MALDI-MS最常用的基质。然而,基质干扰和对不同代谢物的强烈变化的敏感性使得寻找替代基质成为可取的,以便鉴定具有不同化学背景和/或有利于不同分析物范围的化合物。我们测试了一系列潜在的负模式MALDI矩阵的性能,该矩阵具有29种代谢产物的混合物,其中包含氨基酸,核苷酸磷酸盐和Krebs循环中间体。虽然发现乳酸乙四氢吡啶可在低飞摩尔范围内为低核苷酸范围的核苷酸磷酸盐,氨基酸和克雷布斯循环中间体提供检测限(LOD),但4-氨基-2-甲基喹啉对大多数代谢物而言在小孔范围内均具有检测限,但与9AA和乙AA啶相比,能够电离更广泛的分析物。

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