Analysis of interactions between proteins and fatty acids or cholesterol using a fatty acid/cholesterol pull-down assay

Anal Biochem. 2013 May 15;436(2):75-7. doi: 10.1016/j.ab.2013.01.026. Epub 2013 Jan 31.

Abstract

Specific interactions between the polar head groups of membrane lipids and proteins have been described previously. In contrast, the specificity of the interaction between lipid acyl chains with proteins is less understood. By combining a fatty acid or cholesterol pull-down assay with Western blot analysis or mass spectrometry, we identified transmembrane and cytosolic proteins that bound preferentially to short or long acyl chains or to cholesterol. Thus, this approach allows identification of specific fatty acid-protein or cholesterol-protein interactions.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Signal Transducing / metabolism
  • Amino Acyl-tRNA Synthetases / metabolism
  • Biochemistry / methods*
  • Blotting, Western
  • Cell Cycle Proteins / metabolism
  • Cholesterol / analysis
  • Cholesterol / metabolism*
  • Cytosol / chemistry
  • Cytosol / metabolism
  • Electrophoresis, Polyacrylamide Gel
  • Fatty Acids / analysis
  • Fatty Acids / chemistry
  • Fatty Acids / metabolism*
  • Glyceraldehyde-3-Phosphate Dehydrogenases / metabolism
  • Humans
  • Hydrophobic and Hydrophilic Interactions
  • Jurkat Cells
  • Lymphocyte Specific Protein Tyrosine Kinase p56(lck) / metabolism
  • Mass Spectrometry / methods
  • Membrane Lipids / analysis
  • Membrane Lipids / metabolism
  • Membrane Proteins / analysis
  • Membrane Proteins / metabolism*
  • Nuclear Pore Complex Proteins / metabolism
  • Poly-ADP-Ribose Binding Proteins
  • Receptors, Transferrin / metabolism
  • beta Catenin / metabolism

Substances

  • Adaptor Proteins, Signal Transducing
  • BUB3 protein, human
  • CTNNB1 protein, human
  • Cell Cycle Proteins
  • Fatty Acids
  • LAT protein, human
  • Membrane Lipids
  • Membrane Proteins
  • Nuclear Pore Complex Proteins
  • Nup98 protein, human
  • Poly-ADP-Ribose Binding Proteins
  • Receptors, Transferrin
  • beta Catenin
  • Cholesterol
  • Glyceraldehyde-3-Phosphate Dehydrogenases
  • Lymphocyte Specific Protein Tyrosine Kinase p56(lck)
  • Amino Acyl-tRNA Synthetases