Ion Mobility-Derived Collision Cross Section As an Additional Measure for Lipid Fingerprinting and Identification

被引:236
作者
Paglia, Giuseppe [1 ,2 ]
Angel, Peggi [3 ]
Williams, Jonathan P. [4 ]
Richardson, Keith [4 ]
Olivos, Hernando J. [4 ]
Thompson, J. Will [5 ]
Menikarachchi, Lochana [6 ]
Lai, Steven [4 ]
Walsh, Callee [3 ]
Moseley, Arthur [5 ]
Plumb, Robert S. [4 ,7 ]
Grant, David F. [6 ]
Palsson, Bernhard O. [7 ]
Langridge, James [4 ]
Geromanos, Scott [4 ]
Astarite, Giuseppe [4 ,8 ]
机构
[1] Ist Zooprofilatt Sperimentale Puglia & Basilicata, Foggia, Italy
[2] Univ Iceland, Ctr Syst Biol, Reykjavik, Iceland
[3] Protea Biosci Grp Inc, Morgantown, WV 26505 USA
[4] Waters Corp, Milford, MA 01757 USA
[5] Duke Prote Core Facil, Durham, NC 27708 USA
[6] Univ Connecticut, Dept Pharmaceut Sci, Storrs, CT 06268 USA
[7] Univ London Imperial Coll Sci Technol & Med, Fac Med, Dept Surg & Canc, London, England
[8] Georgetown Univ, Dept Biochem & Mol & Cellular Biol, Washington, DC 20057 USA
基金
欧洲研究理事会;
关键词
MASS-SPECTROMETRIC ANALYSIS; STRUCTURAL-CHARACTERIZATION; PHOSPHOLIPIDS; RESOLUTION; DATABASE; BRAIN; GAS; MS; CHOLESTEROL; SEPARATION;
D O I
10.1021/ac503715v
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Despite recent advances in analytical and computational chemistry, lipid identification remains a significant challenge in lipidomics. Ion-mobility spectrometry provides an accurate measure of the molecules rotationally averaged collision cross-section (CCS) in the gas phase and is thus related to ionic shape. Here, we investigate the use of CCS as a highly specific molecular descriptor for identifying lipids in biological samples. Using traveling wave ion mobility mass spectrometry (MS), we measured the CCS values of over 200 lipids within multiple chemical classes. CCS values derived from ion mobility were not affected by instrument settings or chromatographic conditions, and they were highly reproducible on instruments located in independent laboratories (interlaboratory RSD < 3% for 98% of molecules). CCS values were used as additional molecular descriptors to identify brain lipids using a variety of traditional lipidomic approaches. The addition of CCS improved the reproducibility of analysis in a liquid chromatography-MS workflow and maximized the separation of isobaric species and the signal-to-noise ratio in direct-MS analyses (e.g., shotgun lipidomics and MS imaging). These results indicate that adding CCS to databases and lipidomics workflows increases the specificity and selectivity of analysis, thus improving the confidence in lipid identification compared to traditional analytical approaches. The CCS/accurate-mass database described here is made publicly available.
引用
收藏
页码:1137 / 1144
页数:8
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