High Throughput Quantitative Glycomics and Glycoform-focused Proteomics of Murine Dermis and Epidermis
Despite recent advances in our understanding of the significance of the protein glycosylation, the throughput of protein glycosylation analysis is still too low to be applied to the exhaustive glycoproteomic analysis. Aiming to elucidate the N -glycosylation of murine epidermis and dermis glycoprote...
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Veröffentlicht in: | Molecular & cellular proteomics 2005-12, Vol.4 (12), p.1977-1989 |
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Zusammenfassung: | Despite recent advances in our understanding of the significance of the protein glycosylation, the throughput of protein glycosylation
analysis is still too low to be applied to the exhaustive glycoproteomic analysis. Aiming to elucidate the N -glycosylation of murine epidermis and dermis glycoproteins, here we used a novel approach for focused proteomics. A gross
N -glycan profiling (glycomics) of epidermis and dermis was first elucidated both qualitatively and quantitatively upon N -glycan derivatization with novel, stable isotope-coded derivatization reagents followed by MALDI-TOF(/TOF) analysis. This
analysis revealed distinct features of the N -glycosylation profile of epidermis and dermis for the first time. A high abundance of high mannose type oligosaccharides
was found to be characteristic of murine epidermis glycoproteins. Based on this observation, we performed high mannose type
glycoform-focused proteomics by direct tryptic digestion of protein mixtures and affinity enrichment. We identified 15 glycoproteins
with 19 N -glycosylation sites that carry high mannose type glycans by off-line LC-MALDI-TOF/TOF mass spectrometry. Moreover the relative
quantity of microheterogeneity of different glycoforms present at each N -glycan binding site was determined. Glycoproteins identified were often contained in lysosomes ( e.g. cathepsin L and γ-glutamyl hydrolase), lamellar granules ( e.g. glucosylceramidase and cathepsin D), and desmosomes ( e.g. desmocollin 1, desmocollin 3, and desmoglein). Lamellar granules are organelles found in the terminally differentiating cells
of keratinizing epithelia, and desmosomes are intercellular junctions in vertebrate epithelial cells, thus indicating that
N -glycosylation of tissue-specific glycoproteins may contribute to increase the relative proportion of high mannose glycans.
The striking roles of lysosomal enzymes in epidermis during lipid remodeling and desquamation may also reflect the observed
high abundance of high mannose glycans. |
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ISSN: | 1535-9476 1535-9484 |
DOI: | 10.1074/mcp.M500203-MCP200 |