Ubiquitination of an artificial RING finger without a substrate and a tag

J Pept Sci. 2012 Feb;18(2):135-9. doi: 10.1002/psc.1426. Epub 2011 Nov 24.

Abstract

Alpha-helical region substitution was applied to the SIAH1 and EL5 RING fingers. The Williams-Beuren syndrome transcription factor (WSTF) PHD_SIAH1 and WSTF PHD_EL5 RING fingers were created as the artificial ubiquitin-ligating enzyme (E3). These fingers possess E3 activities of mono-ubiquitination and poly-ubiquitination, respectively, with ubiquitin-conjugating enzyme (E2)-binding capabilities. Artificial E3s bind two zinc atoms and adopt a zinc-dependent ordered structure and ubiquitinate upon themselves without a substrate and a tag. Ubiquitination experiments using biotinylated ubiquitin showed that the WSTF PHD_EL5 RING finger is poly-ubiquitinated via residue Lys(63) of ubiquitin. Substitution of alpha-helical region might be applicable to various RING fingers with mono-ubiquitination or poly-ubiquitination.

MeSH terms

  • Amino Acid Sequence
  • Molecular Sequence Data
  • Peptides / chemical synthesis
  • Peptides / chemistry*
  • Polyubiquitin / chemistry
  • Protein Binding
  • Protein Folding
  • Protein Structure, Secondary
  • RING Finger Domains
  • Substrate Specificity
  • Transcription Factors / chemical synthesis
  • Transcription Factors / chemistry*
  • Ubiquitin-Conjugating Enzymes / chemical synthesis
  • Ubiquitin-Conjugating Enzymes / chemistry
  • Ubiquitin-Protein Ligases / chemical synthesis
  • Ubiquitin-Protein Ligases / chemistry
  • Ubiquitination
  • Zinc / chemistry

Substances

  • BAZ1B protein, human
  • Peptides
  • Transcription Factors
  • Polyubiquitin
  • Ubiquitin-Conjugating Enzymes
  • Ubiquitin-Protein Ligases
  • Zinc