The Cation-π Box Is a Specific Phosphatidylcholine Membrane Targeting Motif

Peripheral membrane proteins can be targeted to specific organelles or the plasma membrane by differential recognition of phospholipid headgroups. Although molecular determinants of specificity for several headgroups, including phosphatidylserine and phosphoinositides are well defined, specific recognition of the headgroup of the zwitterionic phosphatidylcholine (PC) is less well understood. In cytosolic proteins the cation-π box provides a suitable receptor for choline recognition and binding through the trimethylammonium moiety. In PC, this moiety might provide a sufficient handle to bind to peripheral proteins via a cation-π cage, where the π systems of two or more aromatic residues are within 4–5 Å of the quaternary amine. We prove this hypothesis by engineering the cation-π box into secreted phosphatidylinositol-specific phospholipase C from Staphylococcus aureus , which lacks specific PC recognition. The N254Y/H258Y variant selectively binds PC-enriched vesicles, and x-ray crystallography reveals N254Y/H258Y binds choline and dibutyroylphosphatidylcholine within the cation-π motif. Such simple PC recognition motifs could be engineered into a wide variety of secondary structures providing a generally applicable method for specific recognition of PC. Background: Specific interactions of peripheral membrane proteins with phosphatidylcholine (PC) are poorly characterized. Results: Staphylococcus aureus phosphatidylinositol-specific phospholipase C has poor affinity for PC. Introduction of two tyrosines generates a specific PC binding site. Conclusion: The PC choline cation interaction with amino acid π systems forms the PC-specific site. Significance: Well defined choline cation-aromatic π interactions may be a general motif to anchor proteins to PC-rich bilayers.