Toward an integrated structural model of the 26S proteasome

Friedrich Förster, Keren Lasker, Stephan Nickell, Andrej Sali, Wolfgang Baumeister

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

The 26S proteasome is the end point of the ubiquitin-proteasome pathway and degrades ubiquitylated substrates. It is composed of the 20S core particle (CP), where degradation occurs, and the 19S regulatory particle (RP), which ensures substrate specificity of degradation. Whereas the CP is resolved to atomic resolution, the architecture of the RP is largely unknown. We provide a comprehensive analysis of the current structural knowledge on the RP, including structures of the RP subunits, physical protein-protein interactions, and cryoelectron microscopy data. These data allowed us to compute an atomic model for the CP-AAA-ATPase subcomplex. In addition to this atomic model, further subunits can be mapped approximately, which lets us hypothesize on the substrate path during its degradation.

Original languageEnglish
Pages (from-to)1666-77
Number of pages12
JournalMolecular & Cellular Proteomics
Volume9
Issue number8
DOIs
Publication statusPublished - Aug 2010
Externally publishedYes

Keywords

  • Animals
  • Cryoelectron Microscopy
  • Models, Molecular
  • Proteasome Endopeptidase Complex
  • Protein Binding
  • Protein Subunits

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