A chemical glycoproteomics platform reveals O-GlcNAcylation of mitochondrial voltage-dependent anion channel 2

Cell Rep. 2013 Oct 31;5(2):546-52. doi: 10.1016/j.celrep.2013.08.048. Epub 2013 Oct 10.

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.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Acetylglucosamine / metabolism
  • Animals
  • Cell Line
  • Electrophoresis, Gel, Pulsed-Field
  • Fluorescent Dyes / chemistry
  • Glycoproteins / metabolism
  • Glycosylation
  • HEK293 Cells
  • Humans
  • Jurkat Cells
  • Mice
  • Mitochondria / metabolism*
  • Proteomics
  • Substrate Specificity
  • Voltage-Dependent Anion Channel 2 / deficiency
  • Voltage-Dependent Anion Channel 2 / genetics
  • Voltage-Dependent Anion Channel 2 / metabolism*

Substances

  • Fluorescent Dyes
  • Glycoproteins
  • VDAC2 protein, human
  • Voltage-Dependent Anion Channel 2
  • Acetylglucosamine