NMR studies on binding sites and aggregation-disassociation of fluorinated surfactant sodium perfluorooctanoate on protein ubiquitin

Biochim Biophys Acta. 2009 Feb;1790(2):134-40. doi: 10.1016/j.bbagen.2008.10.009. Epub 2008 Nov 3.

Abstract

The fluorinated surfactant sodium perfluorooctanoate (SPFO) could bind onto ubiquitin (UBQ) and induce the unfolding of UBQ. By using (15)N-edited heteronuclear single-quantum coherence (HSQC) NMR and (19)F NMR to monitor (15)N-labeled UBQ and SPFO, respectively, the binding sites and the aggregation process of SPFO on UBQ at various SPFO concentrations were observed. A detailed process from specific binding to cooperative binding of SPFO on UBQ, and a detailed structure change of UBQ upon the increase of SPFO concentration were obtained. The refolding of UBQ in UBQ-SPFO complex was carried out by adding cationic surfactant. It was shown that added cationic surfactants formed mixed micelles with SPFO and resulted in the dissociation of the UBQ-SPFO complex, and consequently, most ubiquitin could be refolded to its native state.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Binding Sites
  • Caprylates / pharmacology*
  • Chemical Precipitation
  • Fluorocarbons / pharmacology*
  • Models, Biological
  • Models, Molecular
  • Nuclear Magnetic Resonance, Biomolecular*
  • Protein Binding
  • Protein Folding / drug effects
  • Surface-Active Agents / pharmacology
  • Ubiquitin / chemistry*
  • Ubiquitin / drug effects
  • Ubiquitin / metabolism*

Substances

  • Caprylates
  • Fluorocarbons
  • Surface-Active Agents
  • Ubiquitin
  • perfluorooctanoic acid