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基质辅助激光解吸/电离法同时定量测定干血斑中的(酰基)肉碱和有机酸。

Matrix-assisted laser desorption/ionization for simultaneous quantitation of (acyl-)carnitines and organic acids in dried blood spots.

机构信息

Department of Pediatrics and Adolescent Medicine, Medical University of Vienna, Vienna, Austria.

出版信息

Rapid Commun Mass Spectrom. 2013 Jul 15;27(13):1497-504. doi: 10.1002/rcm.6597.

DOI:10.1002/rcm.6597
PMID:23722684
Abstract

RATIONALE

Screening for inborn errors of metabolism using mass spectrometry is part of nationwide newborn screening programs and involves the detection of disease relevant (acyl-)carnitines and organic acids from dried blood spots. Matrix-Assisted Laser Desorption/Ionization Mass Spectrometry (MALDI-MS) is a well-established tool for proteomics approaches. In recent years, this technique has become more and more integrated in analysis and identification of small metabolites and disease biomarkers in daily clinical laboratories.

METHODS

We used a combination of both MALDI and high-resolution accurate mass (HR/AM) mass spectrometry using a linear ion trap-Orbitrap for the identification of small molecules from dried blood spots that serve as biomarkers for inborn errors of metabolism. The levels of detected metabolite species were compared between healthy newborns and affected patients with various inborn errors of metabolism using isotopically labeled internal standards and new bioinformatics software, respectively.

RESULTS

(Acyl-)carnitine levels from normal and affected patients could be quantified and differentiated. Additionally, using the high resolving power of full scan Orbitrap mass spectrometry and novel software tools we demonstrated the identification and quantification of disease-specific organic acids.

CONCLUSIONS

MALDI-HR/AM and full scan spectra to obtain information for the metabolic status of patients is a promising complementary approach to electrospray ionization mass spectrometry by simplified sample preparation, facilitating the screening of hundreds of metabolites from small sample volumes.

摘要

原理

使用质谱法对先天性代谢缺陷进行筛查是全国新生儿筛查计划的一部分,涉及从干血斑中检测与疾病相关的(酰基)肉碱和有机酸。基质辅助激光解吸/电离质谱(MALDI-MS)是蛋白质组学方法的一种成熟工具。近年来,这项技术在日常临床实验室中小代谢物和疾病生物标志物的分析和鉴定中越来越多地得到应用。

方法

我们使用 MALDI 和高分辨率精确质量(HR/AM)质谱联用,结合线性离子阱-Orbitrap 来鉴定作为先天性代谢缺陷生物标志物的干血斑中的小分子。使用同位素标记的内标和新的生物信息学软件,分别比较了健康新生儿和各种先天性代谢缺陷患者中检测到的代谢物水平。

结果

正常和患病患者的(酰基)肉碱水平可以进行定量和区分。此外,我们利用全扫描 Orbitrap 质谱的高分辨率和新的软件工具,证明了特定疾病有机酸的鉴定和定量。

结论

MALDI-HR/AM 和全扫描谱获得的关于患者代谢状态的信息,是一种有前途的补充方法,与简化的样品制备相比,电喷雾电离质谱法可以更方便地从小样本量中筛选数百种代谢物。

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引用本文的文献

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Rapid method towards proteomic analysis of dried blood spots by MALDI mass spectrometry.通过基质辅助激光解吸电离质谱法对干血斑进行蛋白质组学分析的快速方法。
Clin Mass Spectrom. 2019 Mar 15;12:30-36. doi: 10.1016/j.clinms.2019.03.002. eCollection 2019 Apr.
2
Clinical Metabolomics: The New Metabolic Window for Inborn Errors of Metabolism Investigations in the Post-Genomic Era.临床代谢组学:后基因组时代先天性代谢缺陷研究的新代谢窗口
Int J Mol Sci. 2016 Jul 20;17(7):1167. doi: 10.3390/ijms17071167.