PUBLICATION
Clickable Galactose Analogs for Imaging Glycans in Developing Zebrafish
- Authors
- Daughtry, J.L., Cao, W., Ye, J., Baskin, J.M.
- ID
- ZDB-PUB-200125-7
- Date
- 2020
- Source
- ACS Chemical Biology 15(2): 318-324 (Journal)
- Registered Authors
- Keywords
- none
- MeSH Terms
-
- Alkynes/chemistry
- Animals
- Azides/chemistry
- CHO Cells
- Click Chemistry
- Cricetulus
- Fluoresceins/chemistry
- Galactose/analogs & derivatives*
- Galactose/metabolism*
- Glycoproteins/chemistry
- Glycoproteins/metabolism
- Glycosylation
- HEK293 Cells
- HeLa Cells
- Humans
- Microscopy, Fluorescence
- Polysaccharides/chemistry
- Polysaccharides/metabolism*
- Sulfonic Acids/chemistry
- Uridine Diphosphate Galactose/analogs & derivatives*
- Uridine Diphosphate Galactose/metabolism*
- Zebrafish
- PubMed
- 31976645 Full text @ ACS Chem. Biol.
Citation
Daughtry, J.L., Cao, W., Ye, J., Baskin, J.M. (2020) Clickable Galactose Analogs for Imaging Glycans in Developing Zebrafish. ACS Chemical Biology. 15(2):318-324.
Abstract
Galactose is one of only nine monosaccharide precursors used to build complex glycans in vertebrates. Defects in galactose metabolism cause galactosemia and lysosomal storage diseases, and the ability to visualize metabolic flux through these pathways would help to understand mechanisms underlying disease pathogenesis. Bioorthogonal metabolic reporters are widely used tools to image glycan biosynthesis, but to date, no galactose analogs have capitalized on this strategy. We demonstrate that the galactose salvage pathway is remarkably intolerant of unnatural galactose and galactose-1-phosphate analogs. Subtle modifications to uridine diphosphate galactose (UDP-Gal), the universal donor for galactosyltransferases, however, yielded effective metabolic probes for labeling glycans in vivo. We applied 6-alkynyl UDP-Gal, followed by click chemistry tagging, to visualize glycosylation during zebrafish development, revealing a striking accumulation into glycan-rich ridges within the organism's enveloping layer. UDP-Gal analogs represent a new class of glycan metabolic probes for revealing physiological and pathological changes in glycosylation in vivo.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping