Nanobody-targeted E3-ubiquitin ligase complex degrades nuclear proteins

Sci Rep. 2015 Sep 16:5:14269. doi: 10.1038/srep14269.

Abstract

Targeted protein degradation is a powerful tool in determining the function of specific proteins or protein complexes. We fused nanobodies to SPOP, an adaptor protein of the Cullin-RING E3 ubiquitin ligase complex, resulting in rapid ubiquitination and subsequent proteasome-dependent degradation of specific nuclear proteins in mammalian cells and zebrafish embryos. This approach is easily modifiable, as substrate specificity is conferred by an antibody domain that can be adapted to target virtually any protein.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Gene Expression
  • Genes, Reporter
  • HMGA2 Protein / genetics
  • HMGA2 Protein / metabolism
  • Nuclear Proteins / genetics
  • Nuclear Proteins / metabolism*
  • Protein Binding
  • Proteolysis
  • RNA Interference
  • Recombinant Fusion Proteins / genetics
  • Recombinant Fusion Proteins / metabolism
  • Single-Domain Antibodies / immunology
  • Single-Domain Antibodies / metabolism*
  • Ubiquitin-Protein Ligase Complexes / immunology
  • Ubiquitin-Protein Ligase Complexes / metabolism*
  • Ubiquitin-Protein Ligases / genetics
  • Ubiquitin-Protein Ligases / immunology
  • Ubiquitin-Protein Ligases / metabolism*
  • Ubiquitination
  • Zebrafish

Substances

  • HMGA2 Protein
  • Nuclear Proteins
  • Recombinant Fusion Proteins
  • Single-Domain Antibodies
  • Ubiquitin-Protein Ligase Complexes
  • Ubiquitin-Protein Ligases