Chemical Synthesis and Biological Applications of O-GlcNAcylated Peptides and Proteins

Chembiochem. 2021 Jun 2;22(11):1854-1870. doi: 10.1002/cbic.202000843. Epub 2021 Mar 3.

Abstract

All human cells use O-GlcNAc protein modifications (O-linked N-acetylglucosamine) to rapidly adapt to changing nutrient and stress conditions through signaling, epigenetic, and proteostasis mechanisms. A key challenge for biologists in defining precise roles for specific O-GlcNAc sites is synthetic access to homogenous isoforms of O-GlcNAc proteins, a result of the non-genetically templated, transient, and heterogeneous nature of O-GlcNAc modifications. Toward a solution, this review details the state of the art of two strategies for O-GlcNAc protein modification: advances in "bottom-up" O-GlcNAc peptide synthesis and direct "top-down" installation of O-GlcNAc on full proteins. We also describe key applications of synthetic O-GlcNAc peptide and protein tools as therapeutics, biophysical structure-function studies, biomarkers, and as disease mechanistic probes to advance translational O-GlcNAc biology.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Acetylglucosamine / chemistry
  • Acetylglucosamine / metabolism*
  • Carbohydrate Conformation
  • Humans
  • Models, Molecular
  • Peptides / chemistry
  • Peptides / metabolism*
  • Protein Processing, Post-Translational
  • Proteins / chemistry
  • Proteins / metabolism*

Substances

  • Peptides
  • Proteins
  • Acetylglucosamine