The creation of the artificial RING finger from the cross-brace zinc finger by alpha-helical region substitution

Biochem Biophys Res Commun. 2010 Apr 16;394(4):972-5. doi: 10.1016/j.bbrc.2010.03.100. Epub 2010 Mar 20.

Abstract

The creation of the artificial RING finger as ubiquitin-ligating enzyme (E3) has been demonstrated. In this study, by the alpha-helical region substitution between the EL5 RING finger and the Williams-Beuren syndrome transcription factor (WSTF) PHD finger, the artificial E3 (WSTF PHD_RING finger) was newly created. The experiments of the chemical modification of residues Cys and the circular dichroism spectra revealed that the WSTF PHD_RING finger binds two zinc atoms and adopts the zinc-dependent ordered-structure. In the substrate-independent ubiquitination assay, the WSTF PHD_RING finger functions as E3 and was poly- or mono-ubiquitinated. The present strategy is very simple and convenient, and consequently it might be widely applicable to the creation of various artificial E3 RING fingers with the specific ubiquitin-conjugating enzyme (E2)-binding capability.

MeSH terms

  • Amino Acid Sequence
  • Cysteine / chemistry
  • Humans
  • Molecular Sequence Data
  • Protein Folding
  • Protein Structure, Secondary
  • RING Finger Domains*
  • Transcription Factors / chemistry*
  • Ubiquitin-Protein Ligases / chemical synthesis*
  • Ubiquitin-Protein Ligases / chemistry
  • Ubiquitination
  • Zinc / chemistry
  • Zinc Fingers*

Substances

  • BAZ1B protein, human
  • Transcription Factors
  • Ubiquitin-Protein Ligases
  • Zinc
  • Cysteine