A Sweet Embrace: Control of Protein-Protein Interactions by O-Linked β-N-Acetylglucosamine.
Abstract
O-Linked β-N-acetylglucosamine (O-GlcNAc) is a critical post-translational modification
(PTM) of thousands of intracellular proteins. Reversible O-GlcNAcylation governs many
aspects of cell physiology and is dysregulated in numerous human diseases. Despite
this broad pathophysiological significance, major aspects of O-GlcNAc signaling remain
poorly understood, including the biochemical mechanisms through which O-GlcNAc transduces
information. Recent work from many laboratories, including our own, has revealed that
O-GlcNAc, like other intracellular PTMs, can control its substrates' functions by
inhibiting or inducing protein-protein interactions. This dynamic regulation of multiprotein
complexes exerts diverse downstream signaling effects in a range of processes, cell
types, and organisms. Here, we review the literature about O-GlcNAc-regulated protein-protein
interactions and suggest important questions for future studies in the field.
Type
Journal articleSubject
AnimalsHumans
Acetylglucosamine
Biochemistry
Signal Transduction
Protein Processing, Post-Translational
Aminoacylation
Models, Biological
Protein Interaction Domains and Motifs
Protein Multimerization
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https://hdl.handle.net/10161/19692Published Version (Please cite this version)
10.1021/acs.biochem.7b00871Publication Info
Tarbet, Heather J; Toleman, Clifford A; & Boyce, Michael (2018). A Sweet Embrace: Control of Protein-Protein Interactions by O-Linked β-N-Acetylglucosamine.
Biochemistry, 57(1). pp. 13-21. 10.1021/acs.biochem.7b00871. Retrieved from https://hdl.handle.net/10161/19692.This is constructed from limited available data and may be imprecise. To cite this
article, please review & use the official citation provided by the journal.
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Show full item recordScholars@Duke
Michael Scott Boyce
Associate Professor of Biochemistry
The Boyce Lab studies mammalian cell signaling through protein glycosylation. For
the latest news, project information and publications from our group, please visit
our web site at http://www.boycelab.org or follow us on Twitter at https://twitter.com/BoyceLab.

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