Name:
Adduct:
Polarity:
Z:
m/z:
±:
CCS: Å2
±: %
SMI:
Type:

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1
May, J. C. et al. Conformational Ordering of Biomolecules in the Gas Phase: Nitrogen Collision Cross Sections Measured on a Prototype High Resolution Drift Tube Ion Mobility-Mass Spectrometer. Anal. Chem. 86, 2107–2116 (2014).


2
Paglia, G. et al. Ion Mobility Derived Collision Cross Sections to Support Metabolomics Applications. Anal. Chem. 86, 3985–3993 (2014).


3
Groessl, M., Graf, S. & Knochenmuss, R. High resolution ion mobility-mass spectrometry for separation and identification of isomeric lipids. Analyst 140, 6904–6911 (2015).


4
Zhou, Z., Shen, X., Tu, J. & Zhu, Z.-J. Large-Scale Prediction of Collision Cross-Section Values for Metabolites in Ion Mobility-Mass Spectrometry. Anal. Chem. 88, 11084–11091 (2016).


5
Hines, K. M., Herron, J. & Xu, L. Assessment of altered lipid homeostasis by HILIC-ion mobility-mass spectrometry-based lipidomics. The Journal of Lipid Research 58, 809–819 (2017).


6
Bijlsma, L. et al. Prediction of Collision Cross-Section Values for Small Molecules: Application to Pesticide Residue Analysis. Anal. Chem. 89, 6583–6589 (2017).


7
Hines, K. M., Ross, D. H., Davidson, K. L., Bush, M. F. & Xu, L. Large-Scale Structural Characterization of Drug and Drug-Like Compounds by High-Throughput Ion Mobility-Mass Spectrometry. Anal. Chem. 89, 9023–9030 (2017).


8
Stow, S. M. et al. An Interlaboratory Evaluation of Drift Tube Ion Mobility–Mass Spectrometry Collision Cross Section Measurements. Anal. Chem. 89, 9048–9055 (2017).


9
Zhou, Z., Tu, J., Xiong, X., Shen, X. & Zhu, Z.-J. LipidCCS: Prediction of Collision Cross-Section Values for Lipids with High Precision To Support Ion Mobility–Mass Spectrometry-Based Lipidomics. Anal. Chem. 89, 9559–9566 (2017).


10
Zheng, X. et al. A structural examination and collision cross section database for over 500 metabolites and xenobiotics using drift tube ion mobility spectrometry. Chem. Sci. 8, 7724–7736 (2017).


11
Hines, K. M. et al. Characterization of the Mechanisms of Daptomycin Resistance among Gram-Positive Bacterial Pathogens by Multidimensional Lipidomics. mSphere 2, 99–16 (2017).


12
Lian, R. et al. Ion mobility derived collision cross section as an additional measure to support the rapid analysis of abused drugs and toxic compounds using electrospray ion mobility time-of-flight mass spectrometry. Anal. Methods 10, 749–756 (2018).


13
Mollerup, C. B., Mardal, M., Dalsgaard, P. W., Linnet, K. & Barron, L. P. Prediction of collision cross section and retention time for broad scope screening in gradient reversed-phase liquid chromatography-ion mobility-high resolution accurate mass spectrometry. Journal of Chromatography A 1542, 82–88 (2018).


14
Righetti, L. et al. Ion mobility-derived collision cross section database: Application to mycotoxin analysis. Analytica Chimica Acta 1014, 50–57 (2018).


15
Tejada-Casado, C. et al. Collision cross section (CCS) as a complementary parameter to characterize human and veterinary drugs. Analytica Chimica Acta 1043, 52–63 (2018).


16
Nichols, C. M. et al. Untargeted Molecular Discovery in Primary Metabolism: Collision Cross Section as a Molecular Descriptor in Ion Mobility-Mass Spectrometry. Anal. Chem. 90, 14484–14492 (2018).


17
Hines, K. M. & Xu, L. Lipidomic consequences of phospholipid synthesis defects in Escherichia coli revealed by HILIC-ion mobility-mass spectrometry. Chemistry and Physics of Lipids 219, 15–22 (2019).


18
Leaptrot, K. L., May, J. C., Dodds, J. N. & McLean, J. A. Ion mobility conformational lipid atlas for high confidence lipidomics. Nature Communications 1–9 (2019).


19
Blaženović, I. et al. Increasing Compound Identification Rates in Untargeted Lipidomics Research with Liquid Chromatography Drift Time–Ion Mobility Mass Spectrometry. Anal. Chem. 90, 10758–10764 (2018).


20
Vasilopoulou, C. G. et al. Trapped ion mobility spectrometry and PASEF enable in-depth lipidomics from minimal sample amounts. Nature Communications 1–11 (2020).


21
Tsugawa, H. et al. MS-DIAL 4: accelerating lipidomics using an MS/MS, CCS, and retention time atlas. bioRxiv 37, 513 (2020).


22
Poland, J. C. et al. Collision Cross Section Conformational Analyses of Bile Acids via Ion Mobility–Mass Spectrometry. Journal of the American Society for Mass Spectrometry 31, 1625–1631 (2020).


23
Dodds, J. et al. Rapid Characterization of Per- and Polyfluoroalkyl Substances (PFAS) by Ion Mobility Spectrometry−Mass Spectrometry (IMS-MS). Anal. Chem. 92, 4427-4435 (2020).


24
Celma, A. et al. Improving Target and Suspect Screening High-Resolution Mass Spectrometry Workflows in Environmental Analysis by Ion Mobility Separation. Environ. Sci. Technol. 54, 15120-15131 (2020)


25
Belova, L. et al. Ion Mobility-High-Resolution Mass Spectrometry (IM-HRMS) for the Analysis of Contaminants of Emerging Concern (CECs): Database Compilation and Application to Urine Samples. Anal. Chem. XXX, XXXX-XXXX (2021)


26
Ross, D. H., et al. High-Throughput Measurement and Machine Learning-Based Prediction of Collision Cross Sections for Drugs and Drug Metabolites. J Am Soc Mass Spectr 33, 1061–1072 (2022).


ID Name Adduct Structure m/z CCS SMI Type Z Ref CCS Type CCS method
CCSBASE_C7B9DA5B95 LPG(15:0) [M-H]- 469.2573 209.66 CCCCCCCCCCCCCCC(=O)OC[C@@H](O)CO[P](O)(=O)OCC(O)CO lipid 1 17 TW calibrated with phosphatidylcholines (ESI+) and phosphatidylethanolamines (ESI-), doubly charged cardiolipins calibrated with poly-DL-alanine
CCSBASE_F97A600159 LPG(16:1) [M-H]- 481.2572 210.68 CCCCCC/C=C/CCCCCCCC(=O)OC[C@@H](O)CO[P](O)(=O)OCC(O)CO lipid 1 17 TW calibrated with phosphatidylcholines (ESI+) and phosphatidylethanolamines (ESI-), doubly charged cardiolipins calibrated with poly-DL-alanine
CCSBASE_34B5F76EF9 LPG(17:1) [M-H]- 495.2713 214.26 CCCCCCC1CC1CCCCCCCC(=O)OC[C@@H](O)CO[P](O)(=O)OCC(O)CO lipid 1 17 TW calibrated with phosphatidylcholines (ESI+) and phosphatidylethanolamines (ESI-), doubly charged cardiolipins calibrated with poly-DL-alanine
CCSBASE_C337342532 LPG(18:1) [M-H]- 509.2874 217.72 CCCCCCCC/C=C/CCCCCCCC(=O)OC[C@@H](O)CO[P](O)(=O)OCC(O)CO lipid 1 17 TW calibrated with phosphatidylcholines (ESI+) and phosphatidylethanolamines (ESI-), doubly charged cardiolipins calibrated with poly-DL-alanine
CCSBASE_20523839A8 LPG(19:1) [M-H]- 523.3039 221.18 CCCCCCCCC1CC1CCCCCCCC(=O)OC[C@@H](O)CO[P](O)(=O)OCC(O)CO lipid 1 17 TW calibrated with phosphatidylcholines (ESI+) and phosphatidylethanolamines (ESI-), doubly charged cardiolipins calibrated with poly-DL-alanine
CCSBASE_A53792D00B CL(63:3) [M-2H]2- 665.4468 394.68 CCCCCCCCCCCCCCC(=O)OCC(CO[P](O)(=O)OCC(O)CO[P](O)(=O)OCC(COC(=O)CCCCCCC\C=C/CCCCCC)OC(=O)CCCCCCC\C=C/CCCCCC)OC(=O)CCCCCCC\C=C/CCCCCC lipid 2 17 TW calibrated with phosphatidylcholines (ESI+) and phosphatidylethanolamines (ESI-), doubly charged cardiolipins calibrated with poly-DL-alanine
CCSBASE_F8ADBDAC85 CL(63:2) [M-2H]2- 666.4562 394.34 CCCCCCCCCCCCCCCC(=O)OCC(CO[P](O)(=O)OCC(O)CO[P](O)(=O)OCC(COC(=O)CCCCCCCCCCCCCC)OC(=O)CCCCCCC\C=C/CCCCCC)OC(=O)CCCCCCC\C=C/CCCCCC lipid 2 17 TW calibrated with phosphatidylcholines (ESI+) and phosphatidylethanolamines (ESI-), doubly charged cardiolipins calibrated with poly-DL-alanine
CCSBASE_EDECE66BEB CL(63:1) [M-2H]2- 667.4612 394.72 CCCCCCCCCCCCCCCC(=O)OCC(CO[P](O)(=O)OCC(O)CO[P](O)(=O)OCC(COC(=O)CCCCCCCCCCCCCC)OC(=O)CCCCCCCCCCCCCCC)OC(=O)CCCCCCC\C=C/CCCCCC lipid 2 17 TW calibrated with phosphatidylcholines (ESI+) and phosphatidylethanolamines (ESI-), doubly charged cardiolipins calibrated with poly-DL-alanine
CCSBASE_776337A544 CL(64:3) [M-2H]2- 672.4562 397.47 CCCCCCCCCCCCCCCC(=O)OCC(CO[P](O)(=O)OCC(O)CO[P](O)(=O)OCC(COC(=O)CCCCCCC\C=C/CCCCCC)OC(=O)CCCCCCC\C=C/CCCCCC)OC(=O)CCCCCCC\C=C/CCCCCC lipid 2 17 TW calibrated with phosphatidylcholines (ESI+) and phosphatidylethanolamines (ESI-), doubly charged cardiolipins calibrated with poly-DL-alanine
CCSBASE_A2E2DC0AC6 CL(64:2) [M-2H]2- 673.4638 397.0 CCCCCCCCCCCCCCCC(=O)OCC(CO[P](O)(=O)OCC(O)CO[P](O)(=O)OCC(COC(=O)CCCCCCCCCCCCCCC)OC(=O)CCCCCCC\C=C/CCCCCC)OC(=O)CCCCCCC\C=C/CCCCCC lipid 2 17 TW calibrated with phosphatidylcholines (ESI+) and phosphatidylethanolamines (ESI-), doubly charged cardiolipins calibrated with poly-DL-alanine
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