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MetaboAnalyst 4.0: towards more transparent and integrative metabolomics analysis.MetaboAnalyst 4.0:迈向更透明、更综合的代谢组学分析。
Nucleic Acids Res. 2018 Jul 2;46(W1):W486-W494. doi: 10.1093/nar/gky310.
2
A structural examination and collision cross section database for over 500 metabolites and xenobiotics using drift tube ion mobility spectrometry.使用漂移管离子迁移谱法对500多种代谢物和外源性物质进行结构分析及碰撞截面数据库构建。
Chem Sci. 2017 Nov 1;8(11):7724-7736. doi: 10.1039/c7sc03464d. Epub 2017 Sep 28.
3
Automated flow injection method for the high precision determination of drift tube ion mobility collision cross sections.自动化流动注射法用于高精度测定漂移管离子迁移率碰撞截面。
Analyst. 2018 Mar 26;143(7):1556-1559. doi: 10.1039/c8an00056e.
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The potential of ion mobility-mass spectrometry for non-targeted metabolomics.离子淌度-质谱联用在非靶向代谢组学中的潜力。
Curr Opin Chem Biol. 2018 Feb;42:9-15. doi: 10.1016/j.cbpa.2017.10.015. Epub 2017 Nov 5.
5
Correlating Resolving Power, Resolution, and Collision Cross Section: Unifying Cross-Platform Assessment of Separation Efficiency in Ion Mobility Spectrometry.关联分辨率、分辨率和碰撞截面:离子淌度谱中分离效率的跨平台统一评估。
Anal Chem. 2017 Nov 21;89(22):12176-12184. doi: 10.1021/acs.analchem.7b02827. Epub 2017 Oct 30.
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Adding a new separation dimension to MS and LC-MS: What is the utility of ion mobility spectrometry?向 MS 和 LC-MS 添加新的分离维度:离子淌度谱的实用性是什么?
J Sep Sci. 2018 Jan;41(1):20-67. doi: 10.1002/jssc.201700919. Epub 2017 Nov 23.
7
Harmonizing lipidomics: NIST interlaboratory comparison exercise for lipidomics using SRM 1950-Metabolites in Frozen Human Plasma.协调脂质组学:使用冷冻人血浆中的 SRM1950-代谢物进行脂质组学的 NIST 实验室间比较研究。
J Lipid Res. 2017 Dec;58(12):2275-2288. doi: 10.1194/jlr.M079012. Epub 2017 Oct 6.
8
Ion Mobility Separations of Isomers based upon Long Path Length Structures for Lossless Ion Manipulations Combined with Mass Spectrometry.基于长路径长度结构的异构体离子迁移分离用于无损离子操纵与质谱联用
ChemistrySelect. 2016 Jul 1;1(10):2396-2399. doi: 10.1002/slct.201600460.
9
Large-Scale Structural Characterization of Drug and Drug-Like Compounds by High-Throughput Ion Mobility-Mass Spectrometry.通过高通量离子淌度-质谱技术对药物和类药物化合物进行大规模结构表征。
Anal Chem. 2017 Sep 5;89(17):9023-9030. doi: 10.1021/acs.analchem.7b01709. Epub 2017 Aug 22.
10
An Interlaboratory Evaluation of Drift Tube Ion Mobility-Mass Spectrometry Collision Cross Section Measurements.漂移管离子迁移-质谱碰撞截面测量的实验室间评估。
Anal Chem. 2017 Sep 5;89(17):9048-9055. doi: 10.1021/acs.analchem.7b01729. Epub 2017 Aug 16.

非靶向分子在初级代谢物中的发现:碰撞截面作为离子淌度-质谱中的分子描述符。

Untargeted Molecular Discovery in Primary Metabolism: Collision Cross Section as a Molecular Descriptor in Ion Mobility-Mass Spectrometry.

机构信息

Department of Chemistry, Center for Innovative Technology, Vanderbilt Institute of Chemical Biology, Vanderbilt Institute for Integrative Biosystems Research and Education, Vanderbilt-Ingram Cancer Center , Vanderbilt University , Nashville , Tennessee 37235 , United States.

出版信息

Anal Chem. 2018 Dec 18;90(24):14484-14492. doi: 10.1021/acs.analchem.8b04322. Epub 2018 Nov 30.

DOI:10.1021/acs.analchem.8b04322
PMID:30449086
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6819070/
Abstract

In this work, we established a collision cross section (CCS) library of primary metabolites based on analytical standards in the Mass Spectrometry Metabolite Library of Standards (MSMLS) using a commercially available ion mobility-mass spectrometer (IM-MS). From the 554 unique compounds in the MSMLS plate library, we obtained a total of 1246 CCS measurements over a wide range of biochemical classes and adduct types. Resulting data analysis demonstrated that the curated CCS library provides broad molecular coverage of metabolic pathways and highlights intrinsic mass-mobility relationships for specific metabolite superclasses. The separation and characterization of isomeric metabolites were assessed, and all molecular species contained within the plate library, including isomers, were critically evaluated to determine the analytical separation efficiency in both the mass ( m/ z) and mobility (CCS/ΔCCS) dimension required for untargeted metabolomic analyses. To further demonstrate the analytical utility of CCS as an additional molecular descriptor, a well-characterized biological sample of human plasma serum (NIST SRM 1950) was examined by LC-IM-MS and used to provide a detailed isomeric analysis of carbohydrate constituents by ion mobility.

摘要

在这项工作中,我们使用市售的离子淌度-质谱联用仪(IM-MS),基于 Mass Spectrometry Metabolite Library of Standards(MSMLS)中的分析标准,建立了基于初级代谢物的碰撞截面(CCS)库。从 MSMLS 板库中的 554 个独特化合物中,我们共获得了 1246 种在广泛生化类和加合物类型下的 CCS 测量值。结果数据分析表明,经过校对的 CCS 库广泛涵盖了代谢途径的分子,突出了特定代谢物超类的固有质量-淌度关系。对同系物代谢物的分离和表征进行了评估,并对板库中包含的所有分子物种(包括同系物)进行了严格评估,以确定在非靶向代谢组学分析中所需的质量(m/z)和淌度(CCS/ΔCCS)维度上的分析分离效率。为了进一步展示 CCS 作为附加分子描述符的分析实用性,我们通过 LC-IM-MS 对具有良好特征的人血浆血清的生物样本(NIST SRM 1950)进行了检查,并利用该样本通过离子淌度对碳水化合物成分进行了详细的同系物分析。

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