N-glycopedia: libraries for native N-glycan structural analysis
4 affiliations
- 1Department of Surgery, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA
- 2Glycomics Core, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA
- 3Protea Glycosciences Pty Ltd., Wollongong, NSW, Australia
- 4Department of Surgery, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA. [email protected]
Abstract
Studies on glycans of glycoproteins are hampered by the lack of standards that reflect the wide diversity in structure typically observed. To this end we have exploited a large library of N -glycan standards comprised of a unique collection of 226 N -glycans including oligomannose, hybrid, and complex-type. We generated a method employing porous graphitized carbon (PGC) and liquid chromatography mass spectrometry (PGC-LC-MS), which can provide a high degree of resolution of underivatized N -glycan structures. Chromatogram libraries arising from these studies include retention time data, diagnostic fragments, and validated structural assignments, providing a robust platform for both targeted and discovery-based glycomics. We refer to this as an N -glycopedia, the first type of resource in which researchers can compare this collective data to N -glycans under study and overcome the limitations of only having compositional data and predicted structures. The technology is easily expandable to include additional N -glycans as new standards become available.
Related
- Accurate structural modelling of protein-glycan recognition with GlycoWeave
- PslG-Mediated Disruption of Pseudomonas aeruginosa Biofilms: A Multi-Omics Investigation of Matrix Glycan Release, Metabolic Reprogramming, and Structural Disintegration
- Structural tuning of native type V fimbriae shapes mechanical specialization in Porphyromonas gingivalis
- Fast structural search for classification of gut bacterial mucin O-glycan degrading enzymes
- Glycan-mediated binding to collagen by a C-type lectin-like domain of the endocytic receptor Endo180 / uPARAP
BibTeX
@article{ashwood2026nglycopedia,
title = {{N-glycopedia: libraries for native N-glycan structural analysis}},
author = {Christopher Ashwood and Richard D. Cummings},
journal = {Nature Communications},
year = {2026},
month = may,
doi = {10.1038/s41467-026-73091-3},
url = {https://doi.org/10.1038/s41467-026-73091-3},
note = {CC BY-NC-ND},
}
RIS
TY - JOUR
TI - N-glycopedia: libraries for native N-glycan structural analysis
AU - Christopher Ashwood
AU - Richard D. Cummings
PY - 2026
DA - 2026/05/20
JO - Nature Communications
DO - 10.1038/s41467-026-73091-3
UR - https://doi.org/10.1038/s41467-026-73091-3
AB - Studies on glycans of glycoproteins are hampered by the lack of standards that reflect the wide diversity in structure typically observed. To this end we have exploited a large library of N -glycan standards comprised of a unique collection of 226 N -glycans including oligomannose, hybrid, and complex-type. We generated a method employing porous graphitized carbon (PGC) and liquid chromatography mass spectrometry (PGC-LC-MS), which can provide a high degree of resolution of underivatized N -glycan structures. Chromatogram libraries arising from these studies include retention time data, diagnostic fragments, and validated structural assignments, providing a robust platform for both targeted and discovery-based glycomics. We refer to this as an N -glycopedia, the first type of resource in which researchers can compare this collective data to N -glycans under study and overcome the limitations of only having compositional data and predicted structures. The technology is easily expandable to include additional N -glycans as new standards become available.
SN - 2041-1723
ER -