Substrate O-glycosylation actively regulates extracellular proteolysis

Protein Sci. 2024 Aug;33(8):e5128. doi: 10.1002/pro.5128.

Abstract

Extracellular proteolysis critically regulates cellular and tissue responses and is often dysregulated in human diseases. The crosstalk between proteolytic processing and other major post-translational modifications (PTMs) is emerging as an important regulatory mechanism to modulate protease activity and maintain cellular and tissue homeostasis. Here, we focus on matrix metalloproteinase (MMP)-mediated cleavages and N-acetylgalactosamine (GalNAc)-type of O-glycosylation, two major PTMs of proteins in the extracellular space. We investigated the influence of truncated O-glycan trees, also referred to as Tn antigen, following the inactivation of C1GALT1-specific chaperone 1 (COSMC) on the general and MMP9-specific proteolytic processing in MDA-MB-231 breast cancer cells. Quantitative assessment of the proteome and N-terminome using terminal amine isotopic labelling of substrates (TAILS) technology revealed enhanced proteolysis by MMP9 within the extracellular proteomes of MDA-MB-231 cells expressing Tn antigen. In addition, we detected substantial modifications in the proteome and discovered novel ectodomain shedding events regulated by the truncation of O-glycans. These results highlight the critical role of mature O-glycosylation in fine-tuning proteolytic processing and proteome homeostasis by modulating protein susceptibility to proteolytic degradation. These data suggest a complex interplay between proteolysis and O-GalNAc glycosylation, possibly affecting cancer phenotypes.

Keywords: LC–MS; MMP9; TAILS; Tn antigen; crosstalk; degradomics; glycosylation; post‐translational modifications; proteolysis; proteomics.

MeSH terms

  • Antigens, Tumor-Associated, Carbohydrate / metabolism
  • Cell Line, Tumor
  • Galactosyltransferases / genetics
  • Galactosyltransferases / metabolism
  • Glycosylation
  • Humans
  • Matrix Metalloproteinase 9 / metabolism
  • Molecular Chaperones
  • Protein Processing, Post-Translational
  • Proteolysis*
  • Proteome / analysis
  • Proteome / metabolism

Substances

  • Matrix Metalloproteinase 9
  • Tn antigen
  • Antigens, Tumor-Associated, Carbohydrate
  • MMP9 protein, human
  • Galactosyltransferases
  • C1GALT1 protein, human
  • C1GALT1C1 protein, human
  • Proteome
  • Molecular Chaperones