research communications
Inhibition of human adipocyte fatty-acid binding protein (FABP4) has been proposed as a treatment for type 2 diabetes, fatty liver disease and atherosclerosis. However, FABP4 displays a naturally low selectivity towards hydrophobic ligands, leading to the possibility of side effects arising from cross-inhibition of other FABP isoforms. In a search for structural determinants of ligand-binding selectivity, the binding of FABP4 towards a group of small molecules structurally related to the nonsteroidal anti-inflammatory drug ibuprofen was analyzed through X-ray crystallography. Several specific hydrophobic interactions are shown to enhance the binding affinities of these compounds, whereas an aromatic edge-to-face interaction is proposed to determine the conformation of bound ligands, highlighting the importance of aromatic interactions in hydrophobic environments.
Supporting information
Portable Document Format (PDF) file https://doi.org/10.1107/S2053230X14027897/hv5268sup1.pdf |
PDB references: FABP4, apo form, 3rzy; complex with (S)-ibuprofen, 3p6h; complex with (R)-ibuprofen, 3p6g; complex with (S)-3-phenylbutyric acid, 3p6f; complex with 3-(4-methoxy-3-methylphenyl)propionic acid, 3p6d; complex with citric acid, 3p6c; complex with 3-(4-methoxyphenyl)propionic acid, 3p6e