Metabolic labeling of glycans with clickable unnatural sugars has enabled glycan analysis in multicellular systems. However, cell-type-specific labeling of glycans in vivo remains challenging. Here we develop genetically encoded metabolic glycan labeling (GeMGL), a cell-type-specific strategy based on a bump-and-hole pair of an unnatural sugar and its matching engineered enzyme. N-pentynylacetylglucosamine (GlcNAl) serves as a bumped analog of N-acetylglucosamine (GlcNAc) that is specifically incorporated into glycans of cells expressing a UDP-GlcNAc pyrophosphorylase mutant, AGX2 F383G . GeMGL with the 1,3-di-O-propionylated GlcNAl (1,3-Pr 2 GlcNAl) and AGX2 F383G pair was demonstrated in cell cocultures, and used for specific labeling of glycans in mouse xenograft tumors. By generating a transgenic mouse line with AGX2 F383G expressed under a cardiomyocyte-specific promoter, we performed specific imaging of cardiomyocyte glycans in the heart and identified 582 cardiomyocyte O-GlcNAcylated proteins with no interference from other cardiac cell types. GeMGL will facilitate cell-type-specific glycan imaging and glycoproteomics in various tissues and disease models.
Keyphrases
- cell surface
- high resolution
- single cell
- heart failure
- type diabetes
- oxidative stress
- dna methylation
- left ventricular
- cell proliferation
- fluorescence imaging
- metabolic syndrome
- skeletal muscle
- staphylococcus aureus
- transcription factor
- mesenchymal stem cells
- signaling pathway
- escherichia coli
- insulin resistance
- photodynamic therapy
- cell cycle arrest
- data analysis