Sec61-mediated transfer of a membrane protein from the endoplasmic reticulum to the proteasome for destruction

Nature. 1996 Dec 5;384(6608):432-8. doi: 10.1038/384432a0.

Abstract

The human cytomegalovirus genome encodes proteins that trigger destruction of newly synthesized major histocompatibility complex (MHC) class I molecules. The human cytomegalovirus gene US2 specifies a product capable of dislocating MHC class I molecules from the endoplasmic reticulum to the cytosol and delivering them to the proteasome. This process involves the Sec61 complex, in what appears to be a reversal of the reaction by which it translocates nascent chains into the endoplasmic reticulum.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adenosine Triphosphate / metabolism
  • Biological Transport, Active
  • Cell Line
  • Cysteine Endopeptidases / metabolism*
  • Cytomegalovirus / immunology
  • Cytosol / metabolism
  • Endoplasmic Reticulum / metabolism*
  • Glycosylation
  • Histocompatibility Antigens Class I / metabolism
  • Humans
  • Membrane Proteins / metabolism*
  • Multienzyme Complexes / metabolism*
  • Proteasome Endopeptidase Complex
  • Protein Folding
  • SEC Translocation Channels
  • Viral Proteins / immunology

Substances

  • Histocompatibility Antigens Class I
  • Membrane Proteins
  • Multienzyme Complexes
  • SEC Translocation Channels
  • Viral Proteins
  • Adenosine Triphosphate
  • Cysteine Endopeptidases
  • Proteasome Endopeptidase Complex