Demonstrates rapid glycophenotyping in melanoma cells, suggesting a new diagnostic tool.
-glycosylated mucin domains present tumor-associated truncated O-glycans that serve as linkers to the lectins, our recognition elements. Embedding six lectins within lubricin enables orthogonal recognition of Gal-GalNAc-terminated oligosaccharides. In an electrochemical culture-plate format, the resulting sensor supports real-time, in situ glycophenotyping of melanoma cells, achieving quantitative agreement to a conventional, end point, lectin microarray. This glycocalyx-mimetic transducer thus enables the rapid, label-free screening of lectin-glycan interactions and the profiling of diagnostically relevant, tumor-associated glycans.
No takes yet. Share an insight, caveat, or question.
Pimenta et al. (2026) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: