Calnexin and other factors that alter translocation affect the rapid binding of ubiquitin to apoB in the Sec61 complex

J Biol Chem. 1998 May 8;273(19):11887-94. doi: 10.1074/jbc.273.19.11887.

Abstract

Several secretory proteins, including apolipoprotein B, have been shown to undergo degradation by proteasomes. We found that the rapid degradation of nascent apolipoprotein B in HepG2 cells was diminished but not abolished by the addition of any of three different inhibitors of proteasomes. Ubiquitin is conjugated to apolipoprotein B that is not assembled with sufficient lipids either during or soon after synthesis. In addition, we found that apolipoprotein B that has entered the endoplasmic reticulum sufficiently to become glycosylated can be degraded by proteasomes. Furthermore, we detected ubiquitin-apolipoprotein B that is associated with the Sec61 complex, the major constituent of the translocational channel. Treatment of cells with monomethylethanolamine or dithiothreitol decreased the translocation of apolipoprotein B and increased the proportion of ubiquitin-conjugated molecules associated with Sec61. Conversely, treatment of cells with oleic acid, which increased the proportion of translocated apolipoprotein B, decreased the amount of ubiquitin-apolipoprotein B in the Sec61 complex. Finally, we found that inhibition of the interaction between calnexin and apolipoprotein B decreases the translocation of apolipoprotein B, increases the ubiquitin-apolipoprotein B in the Sec61 complex, and increases the proteasomal degradation of glycosylated apolipoprotein B. Thus, ubiquitin can be attached to unassembled apolipoprotein B in the Sec61 complex, and this process is affected by factors including calnexin that alter the translocation of apolipoprotein B.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apolipoproteins B / metabolism*
  • Apolipoproteins B / ultrastructure
  • Biological Transport
  • Calcium-Binding Proteins / metabolism*
  • Calnexin
  • Cysteine Endopeptidases / metabolism*
  • Dithiothreitol / pharmacology
  • Endoplasmic Reticulum / metabolism
  • Glycosylation
  • Humans
  • Indolizines / pharmacology
  • Macromolecular Substances
  • Membrane Proteins / metabolism*
  • Multienzyme Complexes / metabolism*
  • Proteasome Endopeptidase Complex
  • Protein Binding
  • Protein Folding
  • SEC Translocation Channels
  • Tumor Cells, Cultured
  • Ubiquitins / metabolism*

Substances

  • Apolipoproteins B
  • Calcium-Binding Proteins
  • Indolizines
  • Macromolecular Substances
  • Membrane Proteins
  • Multienzyme Complexes
  • SEC Translocation Channels
  • Ubiquitins
  • Calnexin
  • Cysteine Endopeptidases
  • Proteasome Endopeptidase Complex
  • castanospermine
  • Dithiothreitol