Analysis of Protein Glycosylation in the ER

Methods Mol Biol. 2018:1691:205-222. doi: 10.1007/978-1-4939-7389-7_16.

Abstract

Protein N-glycosylation is an essential posttranslational modification which is initiated in the endoplasmic reticulum. In plants, the N-glycans play a pivotal role for 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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Endoplasmic Reticulum / metabolism*
  • Endoplasmic Reticulum-Associated Degradation
  • Glycosylation
  • Polysaccharides / metabolism
  • Protein Folding
  • Protein Transport
  • Proteins / metabolism*

Substances

  • Polysaccharides
  • Proteins