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Blm10 protein promotes proteasomal substrate turnover by an active gating mechanism.

For optimal proteolytic function, the central core of the proteasome (core particle (CP) or 20S) has to associate with activators. We investigated the impact of the yeast activator Blm10 on proteasomal peptide and protein degradation. We found enhanced degradation of peptide substrates in the presence of Blm10 and demonstrated that Blm10 has the capacity to accelerate proteasomal turnover of the unstructured protein tau-441 in vitro. Mechanistically, proteasome activation requires the opening of a closed gate, which allows passage of unfolded proteins into the catalytic chamber. Our data indicate that gate opening by Blm10 is achieved via engagement of its C-terminal segment with the CP. Crucial for this activity is a conserved C-terminal YYX motif, with the penultimate tyrosine playing a preeminent role. Thus, Blm10 utilizes a gate opening strategy analogous to the proteasomal ATPases HbYX-dependent mechanism. Because gating incompetent Blm10 C-terminal point mutants confers a loss of function phenotype, we propose that the cellular function of Blm10 is based on CP association and activation to promote the degradation of proteasome substrates.

Pubmed ID: 22025621


  • Dange T
  • Smith D
  • Noy T
  • Rommel PC
  • Jurzitza L
  • Cordero RJ
  • Legendre A
  • Finley D
  • Goldberg AL
  • Schmidt M


The Journal of biological chemistry

Publication Data

December 16, 2011

Associated Grants

  • Agency: PHS HHS, Id: NIH-NIGMS 5R01GM51923
  • Agency: PHS HHS, Id: NIH-NIGMS-043601
  • Agency: PHS HHS, Id: NIH-NIGMS-084228
  • Agency: NIGMS NIH HHS, Id: R01 GM084228
  • Agency: NIGMS NIH HHS, Id: R37 GM043601

Mesh Terms

  • Phenotype
  • Proteasome Endopeptidase Complex
  • Protein Binding
  • Saccharomyces cerevisiae
  • Saccharomyces cerevisiae Proteins