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A Chemical Glycoproteomics Platform Reveals O-GlcNAcylation of Mitochondrial Voltage-Dependent Anion Channel 2

Authors :
Krishnan K. Palaniappan
Matthew J. Hangauer
Timothy J. Smith
Brian P. Smart
Austin A. Pitcher
Emily H. Cheng
Carolyn R. Bertozzi
Michael Boyce
Source :
Cell Reports, Vol 5, Iss 2, Pp 546-552 (2013)
Publication Year :
2013
Publisher :
Elsevier, 2013.

Abstract

Protein modification by O-linked β-N-acetylglucosamine (O-GlcNAc) is a critical cell signaling modality, but identifying signal-specific O-GlcNAcylation events remains a significant experimental challenge. Here, we describe a method for visualizing and analyzing organelle- and stimulus-specific O-GlcNAcylated proteins and use it to identify the mitochondrial voltage-dependent anion channel 2 (VDAC2) as an O-GlcNAc substrate. VDAC2−/− cells resist the mitochondrial dysfunction and apoptosis caused by global O-GlcNAc perturbation, demonstrating a functional connection between O-GlcNAc signaling and mitochondrial physiology through VDAC2. More broadly, our method will enable the discovery of signal-specific O-GlcNAcylation events in a wide array of experimental contexts.

Subjects

Subjects :
Biology (General)
QH301-705.5

Details

Language :
English
ISSN :
22111247
Volume :
5
Issue :
2
Database :
Directory of Open Access Journals
Journal :
Cell Reports
Publication Type :
Academic Journal
Accession number :
edsdoj.06a4f1d546dfb6232a33d03115b5
Document Type :
article
Full Text :
https://doi.org/10.1016/j.celrep.2013.08.048