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Utilizing novel cationic phenylpyridine labeling in glycan profiling by capillary electrophoresis coupled to mass spectrometry

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SMOLKOVA Denisa GREGUŠ Michal CMELIK Richard PÍŽOVÁ Hana JANSEN-VAN Vuuren Ross D BOBÁĽ Pavel LAVICKA Jana

Rok publikování 2025
Druh Článek v odborném periodiku
Časopis / Zdroj Talanta
Fakulta / Pracoviště MU

Farmaceutická fakulta

Citace
www https://pdf.sciencedirectassets.com/271360/1-s2.0-S0039914024X00168/1-s2.0-S0039914024017582/main.pdf?X-Amz-Security-Token=IQoJb3JpZ2luX2VjEL3%2F%2F%2F%2F%2F%2F%2F%2F%2F%2FwEaCXVzLWVhc3QtMSJGMEQCIANSGXsRZGPu1HprEwy%2B1AEldjikegAuRXomTdd4JFhQAiBeNQPmukShH
Doi http://dx.doi.org/10.1016/j.talanta.2024.127376
Klíčová slova Oligosaccharides; Glycans; Labeling; Phenylpyridine; Capillary electrophoresis; Mass spectrometry
Popis This work focuses on profiling N-linked glycans by capillary electrophoresis coupled to mass spectrometry using a novel fluorescent and mass spectrometry (MS) active derivatization tag. The label is based on 2-phenylpyridine bearing tertiary amine and hydrazide functionalities. It provides efficient labeling via hydrazone formation chemistry, promising fluorescence properties, and ionization efficiency in the positive ion MS mode. Electrophoretic analysis in a neutral-coated capillary allowed baseline separation of maltooligosaccharides with limits of detection in nanomolar concentrations. The developed labeling method was successfully applied to the analyses of N-linked glycans released from several glycoproteins such as bovine ribonuclease B, human immunoglobulin G, or chicken albumin.

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