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DOI 10.1021/acs.analchem.6c00380

Медицинская библиотека · Analytical chemistry · 2026

Comprehensive Isomer-Resolved Ganglioside Profiling by HILIC-nanoESI-MS/MS.

Troppmair Nina, Santol Jonas, Baumert Mark, Opálka Lukáš, Assinger Alice, Coman Cristina, Ahrends Robert

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

Gangliosides are structurally complex glycosphingolipids that regulate cellular signaling via interactions with extracellular binding partners and by influencing protein function within the membrane. Their comprehensive analysis remains analytically challenging, in part due to low endogenous abundance, extensive structural diversity, and the frequent occurrence of isomeric species arising from both glycan and ceramide moieties. Here, we present a hydrophilic interaction liquid chromatography (HILIC) nanoelectrospray ionization tandem mass spectrometry (nanoESI-MS/MS) method specifically designed to achieve isomer-resolved analysis and molecular species-level quantification of gangliosides. To improve characterization of low-abundance fatty acyl fragments, the workflow was extended by combining nanoESI with online fraction collection and subsequent direct infusion. The method demonstrated stable chromatographic performance, high sensitivity, and reproducible quantitative results across ten mouse tissues. Application of the workflow enabled quantification of 80 ganglioside molecular species belonging to 18 subclasses and revealed pronounced tissue-specific differences in subclass distribution and ceramide composition. Overall, this study establishes a robust and sensitive platform for comprehensive ganglioside analysis, providing new opportunities to investigate ganglioside diversity, regulation, and function in complex biological systems.

Для цитирования: Troppmair Nina, Santol Jonas, Baumert Mark, Opálka Lukáš, Assinger Alice, Coman Cristina, Ahrends Robert. Comprehensive Isomer-Resolved Ganglioside Profiling by HILIC-nanoESI-MS/MS.. Analytical chemistry. 2026. DOI: 10.1021/acs.analchem.6c00380.

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