Generic structures of cytotoxic liprotides: nano-sized complexes with oleic acid cores and shells of disordered proteins

Chembiochem. 2014 Dec 15;15(18):2693-702. doi: 10.1002/cbic.201402407. Epub 2014 Nov 17.

Abstract

The cytotoxic complex formed between α-lactalbumin and oleic acid (OA) has inspired many studies on protein-fatty acid complexes, but structural insight remains sparse. After having used small-angle X-ray scattering (SAXS) to obtain structural information, we present a new, generic structural model of cytotoxic protein-oleic acid complexes, which we have termed liprotides (lipids and partially denatured proteins). Twelve liprotides formed from seven structurally unrelated proteins and prepared by different procedures all displayed core-shell structures, each with a micellar OA core and a shell consisting of flexible, partially unfolded protein, which stabilizes the OA micelle. The common structure explains similar effects exerted on cells by different liprotides and is consistent with a cargo off-loading of the OA into cell membranes.

Keywords: lipids; micelles; protein folding; protein structures; protein-protein interactions.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cattle
  • Cytotoxins / chemistry*
  • Cytotoxins / pharmacology
  • Hemolysis / drug effects
  • Micelles
  • Oleic Acids / chemistry*
  • Oleic Acids / pharmacology
  • Protein Denaturation
  • Protein Folding
  • Proteins / chemistry*
  • Proteins / pharmacology
  • Scattering, Small Angle
  • X-Ray Diffraction

Substances

  • Cytotoxins
  • Micelles
  • Oleic Acids
  • Proteins