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Dextran as internal calibrant for N-glycan analysis by liquid chromatography coupled to ion mobility-mass spectrometry

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Manz,  Christian
Molecular Physics, Fritz Haber Institute, Max Planck Society;
Department of Chemistry and Biochemistry, Freie Universität Berlin;
Analytical Chemistry, CMC, Silence Therapeutics GmbH;

Götze,  Michael
Molecular Physics, Fritz Haber Institute, Max Planck Society;
Department of Chemistry and Biochemistry, Freie Universität Berlin;

Zappe,  Andreas
Molecular Physics, Fritz Haber Institute, Max Planck Society;
Department of Chemistry and Biochemistry, Freie Universität Berlin;

/persons/resource/persons32738

Pagel,  Kevin
Molecular Physics, Fritz Haber Institute, Max Planck Society;
Department of Chemistry and Biochemistry, Freie Universität Berlin;

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Citation

Manz, C., Götze, M., Frank, C., Zappe, A., & Pagel, K. (2022). Dextran as internal calibrant for N-glycan analysis by liquid chromatography coupled to ion mobility-mass spectrometry. Analytical and Bioanalytical Chemistry, 414(17), 5023-5031. doi:10.1007/s00216-022-04133-0.


Cite as: https://hdl.handle.net/21.11116/0000-000A-8596-6
Abstract
LC–MS is one of the most important tools for the comprehensive characterization of N-glycans. Despite many efforts to speed up glycan analysis via optimized sample preparation (e.g., faster enzyme digestion in combination with instant or rapid labeling dyes), a major bottleneck remains the rather long measurement times of HILIC chromatography. Further compli- cation arises from the necessity to concomitantly calibrate with an external standard to allow for accurate retention times and the conversion into more robust GU values. Here we demonstrate the use of an internal calibration strategy for HILIC chromatography to speed up glycan analysis. By reducing the number of utilized dextran oligosaccharides, the calibrant can be spiked directly into the sample such that external calibration runs are no longer required. The minimized dextran ladder shows accurate GU calibration with a minor deviation of well below 1% and can be applied without modifications in sample preparation or data processing. We further demonstrate the simultaneous use of the minimized dextran ladder as calibrant for the estimation of CCS values in traveling wave ion mobility spectrometry. In both cases, the minimized dextran ladder enables the measurement of calibrant and sample in a single HPLC run without losing information or accuracy.