Proteolytic Cleavage Driven by Glycosylation

J Biol Chem. 2016 Jan 1;291(1):429-34. doi: 10.1074/jbc.C115.698696. Epub 2015 Oct 29.

Abstract

Proteolytic processing of human host cell factor 1 (HCF-1) to its mature form was recently shown, unexpectedly, to occur in a UDP-GlcNAc-dependent fashion within the transferase active site of O-GlcNAc-transferase (OGT) (Lazarus, M. B., Jiang, J., Kapuria, V., Bhuiyan, T., Janetzko, J., Zandberg, W. F., Vocadlo, D. J., Herr, W., and Walker, S. (2013) Science 342, 1235-1239). An interesting mechanism involving formation and then intramolecular rearrangement of a covalent glycosyl ester adduct of the HCF-1 polypeptide was proposed to account for this unprecedented proteolytic activity. However, the key intermediate remained hypothetical. Here, using a model enzyme system for which the formation of a glycosyl ester within the enzyme active site has been shown unequivocally, we show that ester formation can indeed lead to proteolysis of the adjacent peptide bond, thereby providing substantive support for the mechanism of HCF-1 processing proposed.

Keywords: glutamate; glutamyl ester; glycobiology; glycosidase; glycosyl ester; glycosylation; protein processing; protein splicing; proteolysis; pyroglutamate.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Autolysis
  • Glutamates / metabolism
  • Glycosylation
  • Protein Denaturation
  • Proteins / metabolism*
  • Proteolysis*
  • Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
  • beta-Glucosidase / metabolism

Substances

  • Glutamates
  • Proteins
  • beta-Glucosidase

Associated data

  • PDB/4GYW
  • PDB/4PTW