Bifunctional Monosaccharides Preferentially Localize to Nuclear Subcompartments

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • Pavel Barahtjan - , Max Planck Institute of Molecular Cell Biology and Genetics, Swiss Federal Institute of Technology Lausanne (EPFL) (Author)
  • Juan M. Iglesias-Artola - , Max Planck Institute of Molecular Cell Biology and Genetics (Author)
  • Kristin Böhlig - , Max Planck Institute of Molecular Cell Biology and Genetics (Author)
  • Annett Lohmann - , Max Planck Institute of Molecular Cell Biology and Genetics (Author)
  • André Nadler - , Max Planck Institute of Molecular Cell Biology and Genetics, Clusters of Excellence PoL: Physics of Life (Author)

Abstract

Recent progress in glycan research has been driven by widespread implementations of metabolic oligosaccharide engineering. Complementing existing approaches, we here introduce bifunctional, UV-crosslinkable, and clickable N-acetylglucosamine and N-acetylgalactosamine analogues, which enable direct visualization of the intracellular probe distribution as well as distinguishing monomeric and macromolecule-bound fractions. Using this feature, we find that monomeric N-acetylmonosaccharides partition into RNA-rich nuclear compartments such as nuclear speckles and nucleoli. This suggests the existence of spatially separated N-acetylmonosaccharide pools within the nucleoplasm. Taken together, bifunctional N-acetylmonosaccharide probes are versatile discovery tools for probing intracellular localization of monosaccharides.

Details

Original languageEnglish
Article numbere70373
JournalChemBioChem
Volume27
Issue number10
Publication statusPublished - 27 May 2026
Peer-reviewedYes

External IDs

PubMed 42144895

Keywords

Keywords

  • click-chemistry, monosaccharide, nuclear compartments, sugar imaging