Metabolic chemical reports have fundamentally changed the way researchers study glycosylation. However, when administered as per--acetylated sugars, reporter molecules can participate in nonspecific chemical labeling of cysteine residues termed -glycosylation. Without detailed proteomic analyses, these labeling events can be indistinguishable from bona fide enzymatic labeling convoluting experimental results. Here, we report a solution in the synthesis and characterization of two reporter molecules functionalized at the anomeric position with hexanoic acid: 1-Hex-GlcNAlk and 1-Hex-6AzGlcNAc. Both reporters exhibit robust labeling over background with negligible amounts of nonspecific chemical labeling in cell lysates. This strategy serves as a template for the design of future reporter molecules allowing for more reliable interpretation of results.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8865331PMC
http://dx.doi.org/10.1021/acschembio.1c00470DOI Listing

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