Enhanced protocol for quantitative N-linked glycomics analysis using Individuality Normalization when Labeling with Isotopic Glycan Hydrazide Tags (INLIGHT)™
Autor: | Erin S. Baker, Karen E Butler, Jaclyn Gowen Kalmar, David C. Muddiman |
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Rok vydání: | 2020 |
Předmět: |
Male
PNGase F Glycan Glycosylation 02 engineering and technology Orbitrap Mass spectrometry 01 natural sciences Biochemistry Article Analytical Chemistry law.invention Glycomics chemistry.chemical_compound Polysaccharides Tandem Mass Spectrometry law Humans Peptide-N4-(N-acetyl-beta-glucosaminyl) Asparagine Amidase Fetuins Derivatization Chromatography Reverse-Phase Chromatography biology Hydrophilic interaction chromatography 010401 analytical chemistry 021001 nanoscience & nanotechnology Fetuin 0104 chemical sciences carbohydrates (lipids) chemistry biology.protein Female 0210 nano-technology |
Zdroj: | Anal Bioanal Chem |
ISSN: | 1618-2650 1618-2642 |
DOI: | 10.1007/s00216-020-02892-2 |
Popis: | The analysis of N-linked glycans using liquid chromatography and mass spectrometry (LC-MS) presents significant challenges, particularly owing to their hydrophilic nature. To address these difficulties, a variety of derivatization methods has been developed to facilitate improved ionization and detection sensitivity. One such method, the Individuality Normalization when Labeling with Isotopic Glycan Hydrazide Tags (INLIGHT)™ strategy for labeling glycans, has previously been utilized in the analysis of N- and O-linked glycans in biological samples. To assess the maximum sensitivity and separability of the INLIGHT ™ preparation and analysis pipeline, several critical steps were investigated. First, recombinant and nonrecombinant sources of PNGase F were compared to assess variations in the released glycans. Second, modifications in the INLIGHT™ derivatization step were evaluated including temperature optimization, solvent composition changes, and reaction condition length and tag concentration. Optimization of the modified method resulted in 20–100 times greater peak areas for the detected N-linked glycans in fetuin and horseradish peroxidase compared to the standard method. Furthermore, the identification of low abundance glycans, such as (Fuc)(1)(Gal)(2)(GlcNAc)(4)(Man)(3)(NeuAc)(1) and (Gal)(3)(GlcNAc)(5)(Man)(3)(NeuAc)(3,) was possible. Finally, the optimal LC setup for the INLIGHT™ derivatized N-linked glycan analyses was found to be a C18 reverse-phase (RP) column with mobile phases typical of RPLC. |
Databáze: | OpenAIRE |
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