Multivalent Mechanism of Membrane Insertion by the FYVE Domain

• Published in: The Journal of biological chemistry Vol. 279; no. 4; pp. 3050 - 3057
• Main Authors: Kutateladze, Tatiana G., Capelluto, Daniel G.S., Ferguson, Colin G., Cheever, Matthew L., Kutateladze, Andrei G., Prestwich, Glenn D., Overduin, Michael
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 23.01.2004; American Society for Biochemistry and Molecular Biology
• Subjects: Binding Sites; Cell Membrane - chemistry; Cell Membrane - metabolism; Humans; Membrane Proteins - chemistry; Membrane Proteins - metabolism; Models, Molecular; Protein Binding; Protein Conformation; Protein Structure, Tertiary; Protein Transport; Vesicular Transport Proteins
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1074/jbc.M309007200

Targeting of a wide variety of proteins to membranes involves specific recognition of phospholipid head groups and insertion into lipid bilayers. For example, proteins that contain FYVE domains are recruited to endosomes through interaction with phosphatidylinositol 3-phosphate (PtdIns(3)P). However, the structural mechanism of membrane docking and insertion by this domain remains unclear. Here, the depth and angle of micelle insertion and the lipid binding properties of the FYVE domain of early endosome antigen 1 are estimated by NMR spectroscopy. Spin label probes incorporated into micelles identify a hydrophobic protuberance that inserts into the micelle core and is surrounded by interfacially active polar residues. A novel proxyl PtdIns(3)P derivative is developed to map the position of the phosphoinositide acyl chains, which are found to align with the membrane insertion element. Dual engagement of the FYVE domain with PtdIns(3)P and dodecylphosphocholine micelles yields a 6-fold enhancement of affinity. The additional interaction of phosphatidylserine with a conserved basic site of the protein further amplifies the micelle binding affinity and dramatically alters the angle of insertion. Thus, the FYVE domain is targeted to endosomes through the synergistic action of stereospecific PtdIns(3)P head group ligation, hydrophobic insertion and electrostatic interactions with acidic phospholipids.