Metabolomics Core Facility, European Molecular Biology Laboratory (EMBL), Heidelberg, Germany.
Structural and Computational Biology Unit, EMBL, Heidelberg, Germany.
Metabolomics. 2024 Oct 13;20(6):114. doi: 10.1007/s11306-024-02176-1.
Over the past two decades, liquid chromatography-mass spectrometry (LC-MS)-based metabolomics has experienced significant growth, playing a crucial role in various scientific disciplines. However, despite these advance-ments, metabolite identification (MetID) remains a significant challenge. To address this, stringent MetID requirements were established, emphasizing the necessity of aligning experimental data with authentic reference standards using multiple criteria. Establishing dependable methods and corresponding libraries is crucial for instilling confidence in MetID and driving further progress in metabolomics.
The EMBL-MCF 2.0 LC-MS/MS method and public library was designed to facilitate both targeted and untargeted metabolomics with exclusive focus on endogenous, polar metabolites, which are known to be challenging to analyze due to their hydrophilic nature. By accompanying spectral data with robust retention times obtained from authentic standards and low-adsorption chromatography, high confidence MetID is achieved and accessible to the metabolomics community.
The library is built on hydrophilic interaction liquid chromatography (HILIC) and state-of-the-art low adsorption LC hardware. Both high-resolution tandem mass spectra and manually optimized multiple reaction monitoring (MRM) transitions were acquired on an Orbitrap Exploris 240 and a QTRAP 6500+, respectively.
Implementation of biocompatible HILIC has facilitated the separation of isomeric metabolites with significant enhancements in both selectivity and sensitivity. The resulting library comprises a diverse collection of more than 250 biologically relevant metabolites. The methodology was successfully applied to investigate a variety of biological matrices, with exemplary findings showcased using murine plasma samples.
Our work has resulted in the development of the EMBL-MCF 2.0 library, a powerful resource for sensitive metabolomics analyses and high-confidence MetID. The library is freely accessible and available in the universal .msp file format under the CC-BY 4.0 license: mona.fiehnlab.ucdavis.edu https://mona.fiehnlab.ucdavis.edu/spectra/browse?query=exists(tags.text:%27EMBL-MCF_2.0_HRMS_Library%27) , EMBL-MCF 2.0 HRMS https://www.embl.org/groups/metabolomics/instrumentation-and-software/#MCF-library .
在过去的二十年中,基于液相色谱-质谱(LC-MS)的代谢组学经历了显著的发展,在各个科学领域发挥了关键作用。然而,尽管取得了这些进展,代谢物鉴定(MetID)仍然是一个重大挑战。为此,建立了严格的 MetID 要求,强调必须使用多种标准将实验数据与真实参考标准对齐。建立可靠的方法和相应的库对于在 MetID 中建立信心并推动代谢组学的进一步发展至关重要。
EMBL-MCF 2.0 LC-MS/MS 方法和公共库旨在促进靶向和非靶向代谢组学,专门关注内源性极性代谢物,由于其亲水性,这些代谢物的分析具有挑战性。通过将光谱数据与从真实标准获得的稳健保留时间以及低吸附色谱相结合,实现高可信度的 MetID,并使其可用于代谢组学社区。
该库建立在亲水相互作用液相色谱(HILIC)和最先进的低吸附 LC 硬件之上。高分辨率串联质谱和手动优化的多重反应监测(MRM)跃迁分别在 Orbitrap Exploris 240 和 QTRAP 6500+上获得。
实施生物相容性 HILIC 促进了具有显著增强选择性和灵敏度的同系物代谢物的分离。由此产生的库包含超过 250 种具有生物学相关性的代谢物的多样集合。该方法成功应用于各种生物基质的研究,使用鼠血浆样本展示了典型的发现。
我们的工作导致了 EMBL-MCF 2.0 库的开发,这是一种用于敏感代谢组学分析和高可信度 MetID 的强大资源。该库可免费获取,并以通用.msp 文件格式在 CC-BY 4.0 许可证下提供:mona.fiehnlab.ucdavis.edu https://mona.fiehnlab.ucdavis.edu/spectra/browse?query=exists(tags.text:%27EMBL-MCF_2.0_HRMS_Library%27), EMBL-MCF 2.0 HRMS https://www.embl.org/groups/metabolomics/instrumentation-and-software/#MCF-library 。