Analysis of Protein Glycosylation in the ER

Methods Mol Biol. 2024:2772:221-238. doi: 10.1007/978-1-0716-3710-4_16.

Abstract

Protein N-glycosylation is an essential posttranslational modification which is initiated in the endoplasmic reticulum (ER). In plants, the N-glycans play a pivotal role in protein folding and quality control. Through the interaction of glycan processing and binding reactions mediated by ER-resident glycosidases and specific carbohydrate-binding proteins, the N-glycans contribute to the adoption of a native protein conformation. Properly folded glycoproteins are released from these processes and allowed to continue their transit to the Golgi where further processing and maturation of N-glycans leads to the formation of more complex structures with different functions. Incompletely folded glycoproteins are removed from the ER by a highly conserved degradation process to prevent the accumulation or secretion of misfolded proteins and maintain ER homeostasis. Here, we describe methods to analyze the N-glycosylation status and the glycan-dependent ER-associated degradation process in plants.

Keywords: ERAD; Glycoprotein; N-glycosylation; Oligosaccharyltransferase; Quality control.

MeSH terms

  • Endoplasmic Reticulum*
  • Glycoproteins
  • Glycosylation
  • Polysaccharides
  • Protein Processing, Post-Translational*

Substances

  • Glycoproteins
  • Polysaccharides