Characterization of the specificity of O-GlcNAc reactive antibodies under conditions of starvation and stress

Russell A. Reeves, Albert Lee, Roger Henry, Natasha E. Zachara

Research output: Contribution to journalArticlepeer-review

24 Scopus citations


The dynamic modification of nuclear, cytoplasmic, and mitochondrial proteins by O-linked β-N-acetyl-d-glucosamine (O-GlcNAc) has been shown to regulate over 3000 proteins in a manner analogous to protein phosphorylation. O-GlcNAcylation regulates the cellular stress response and the cell cycle, and is implicated in the etiology of neurodegeneration, type II diabetes, and cancer. The antibody CTD110.6 is often used to detect changes in the O-GlcNAc modification. Recently, it has been demonstrated that CTD110.6 recognizes N-linked N,N′-diacetylchitobiose, which is thought to accumulate in cells experiencing severe glucose deprivation. In this study, we have addressed two questions: (1) Which other antibodies used to detect O-GlcNAc cross-react with N-linked N,N′-diacetylchitobiose? (2) Does N-linked N,N′- diacetylchitobiose accumulate in response to other cellular stressors? To delineate between O-GlcNAc and N-linked N,N′-diacetylchitobiose, we developed a workflow that has been used to confirm the specificity of a variety of O-GlcNAc-specific antibodies. Using this workflow we demonstrated that heat shock, osmotic stress, endoplasmic reticulum stress, oxidative stress, DNA damage, proteasomal inhibition, and ATP depletion induce O-GlcNAcylation but not N-linked N,N′-diacetylchitobiose. Moreover, we demonstrated that while glucose deprivation results in an induction in both O-GlcNAc and N-linked N,N′-diacetylchitobiose, the induction of N-linked N,N′- diacetylchitobiose is exacerbated by the removal of fetal bovine serum.

Original languageEnglish (US)
Pages (from-to)8-18
Number of pages11
JournalAnalytical biochemistry
StatePublished - Jul 15 2014


  • CTD110.6
  • Nutrient deprivation
  • O-GlcNAc
  • Specificity
  • Stress response

ASJC Scopus subject areas

  • Biophysics
  • Biochemistry
  • Molecular Biology
  • Cell Biology


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