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_066E679E67 LPE(0:0/19:1) [M+H]+ 494.3258 221.32 CCCCCCCCC1CC1CCCCCCCC(=O)O[C@H](CO)CO[P]([O-])(=O)OCC[NH3+] lipid 1 17 TW calibrated with phosphatidylcholines (ESI+) and phosphatidylethanolamines (ESI-), doubly charged cardiolipins calibrated with poly-DL-alanine
CCSBASE_CAAC0640DB LPE(0:0/14:0) [M+Na]+ 448.2421 213.66 CCCCCCCCCCCCCC(=O)O[C@H](CO)CO[P]([O-])(=O)OCC[NH3+] lipid 1 17 TW calibrated with phosphatidylcholines (ESI+) and phosphatidylethanolamines (ESI-), doubly charged cardiolipins calibrated with poly-DL-alanine
CCSBASE_FDFE2152A2 LPE(0:0/15:0) [M+Na]+ 462.259 216.84 CCCCCCCCCCCCCCC(=O)O[C@H](CO)CO[P]([O-])(=O)OCC[NH3+] lipid 1 17 TW calibrated with phosphatidylcholines (ESI+) and phosphatidylethanolamines (ESI-), doubly charged cardiolipins calibrated with poly-DL-alanine
CCSBASE_55D30EE2AD LPE(0:0/16:1) [M+Na]+ 474.2596 212.72 CCCCCC/C=C/CCCCCCCC(=O)O[C@H](CO)CO[P]([O-])(=O)OCC[NH3+] lipid 1 17 TW calibrated with phosphatidylcholines (ESI+) and phosphatidylethanolamines (ESI-), doubly charged cardiolipins calibrated with poly-DL-alanine
CCSBASE_CACA12D18F LPE(0:0/16:0) [M+Na]+ 476.2745 220.61 CCCCCCCCCCCCCCCC(=O)O[C@H](CO)CO[P]([O-])(=O)OCC[NH3+] lipid 1 17 TW calibrated with phosphatidylcholines (ESI+) and phosphatidylethanolamines (ESI-), doubly charged cardiolipins calibrated with poly-DL-alanine
CCSBASE_C1CB450602 LPE(0:0/17:1) [M+Na]+ 488.2787 219.32 CCCCCCC1CC1CCCCCCCC(=O)O[C@H](CO)CO[P]([O-])(=O)OCC[NH3+] lipid 1 17 TW calibrated with phosphatidylcholines (ESI+) and phosphatidylethanolamines (ESI-), doubly charged cardiolipins calibrated with poly-DL-alanine
CCSBASE_97E9928DE6 LPE(0:0/18:1) [M+Na]+ 502.2905 220.12 CCCCCCCC/C=C/CCCCCCCC(=O)O[C@H](CO)CO[P]([O-])(=O)OCC[NH3+] lipid 1 17 TW calibrated with phosphatidylcholines (ESI+) and phosphatidylethanolamines (ESI-), doubly charged cardiolipins calibrated with poly-DL-alanine
CCSBASE_447FB6BF72 LPE(0:0/19:1) [M+Na]+ 516.3068 226.07 CCCCCCCCC1CC1CCCCCCCC(=O)O[C@H](CO)CO[P]([O-])(=O)OCC[NH3+] lipid 1 17 TW calibrated with phosphatidylcholines (ESI+) and phosphatidylethanolamines (ESI-), doubly charged cardiolipins calibrated with poly-DL-alanine
CCSBASE_B63503C830 PA(36:01) [M+Na]+ 725.5093 273.4 [C@](COP(=O)(O)O)([H])(OC(CCCCCCC/C=C\CCCCCCCC)=O)COC(CCCCCCCCCCCCCCCCC)=O lipid 1 18 DT stepped-field
CCSBASE_24D3BC3964 PA(36:02) [M+Na]+ 723.4907 272.25 [C@](COP(=O)(O)O)([H])(OC(CCCCCCCCC/C=C\CCCCCCCCCC)=O)COC(CCCCCCC/C=C\CCCC)=O lipid 1 18 DT stepped-field
1 2 ... 711 712 713 714 715 716 717 ... 1698 1699