Abstract
Identifying cell-specific glycan structures in human lungs is critical for understanding the chemistry and mechanisms that guide cell-cell and cell-matrix interactions and determining nuanced functions of specific glycosylation. Our dual-modality omics platform, which uses matrix-assisted laser desorption/ionization (MALDI) mass spectrometry imaging (MSI) to profile glycan chemistry at 50 μm × 50 μm scale, combined with co-detection by indexing (CODEX) to provide cell identification from the exact same tissue section, is a significant step in this direction. It enabled us to detect, differentiate, and reveal chemical properties of N-glycans in the various cell types of a human lung, suggesting the cell-specific function of distinct carbohydrate moieties. This innovative technological combination bridges the gap between the specific protein glycosylation and their cellular origin, paving the way for targeted studies in the lungs and many other human tissues where glycans mediate cell-cell recognition events.
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CITATION STYLE
Veličković, D., Purkerson, J., Bhotika, H., Huyck, H., Clair, G., Pryhuber, G. S., & Anderton, C. (2025). Integrating N-glycan and CODEX imaging reveal cell-specific protein glycosylation in healthy human lung. Molecular Omics, 21(4), 334–342. https://doi.org/10.1039/d4mo00230j
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