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Reveals O-GlcNAcylation profiling in HeLa cells, suggesting its role in stress response.
) approach employing a ketone-functionalized UDP-GalNAc analogue (UDP-GalNLeV) for one-step chemoenzymatic labeling with >96% efficiency, eliminating intermediate reactions and minimizing handling-induced loss. Crucially, oxime-based capture using hydroxylamine-functionalized beads, followed by reversible methoxyamine-mediated release, overcomes the limitations of conventional ketone-based enrichment strategies and eliminates the need for azide-based chemistry. Using the ORO-GlcNAc strategy, we identified 4129 potential O-GlcNAcylation sites in HeLa cells, of which 64.3% were annotated in the O-GlcNAc Atlas, demonstrating the high coverage and enrichment performance of ORO-GlcNAc. Functional studies suggested a potential role of O-GlcNAcylation in the nucleocytoplasmic redistribution of the chromatin remodeler EP400 during stress-granule assembly. This platform thus provides a powerful and versatile tool for advancing the O-GlcNAcylation research.
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Liu et al. (2026) studied this question.
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