O-linked β- N -acetylglucosamine (O-GlcNAc) is a ubiquitous post-translational modification in mammals, decorating thousands of intracellular proteins. O-GlcNAc cycling is an essential regulator of myriad aspects of cell physiology and is dysregulated in numerous human diseases. Notably, O-GlcNAcylation is abundant in the brain and numerous studies have linked aberrant O-GlcNAc signaling to various neurological conditions. However, the complexity of the nervous system and the dynamic nature of protein O-GlcNAcylation have presented challenges for studying of neuronal O-GlcNAcylation. In this context, chemical approaches have been a particularly valuable complement to conventional cellular, biochemical, and genetic methods to understand O-GlcNAc signaling and to develop future therapeutics. Here we review selected recent examples of how chemical tools have empowered efforts to understand and rationally manipulate O-GlcNAcylation in mammalian neurobiology.
Keyphrases
- cerebral ischemia
- endothelial cells
- transcription factor
- stem cells
- single cell
- resting state
- small molecule
- high intensity
- current status
- blood brain barrier
- amino acid
- genome wide
- bone marrow
- white matter
- functional connectivity
- subarachnoid hemorrhage
- mesenchymal stem cells
- protein protein
- binding protein
- pluripotent stem cells