Molecular Determinants of Plasma Cholesteryl Ester Transfer Protein Binding to High Density Lipoproteins

• Published in: The Journal of biological chemistry Vol. 270; no. 19; pp. 11532 - 11542
• Main Authors: Bruce, Can, Davidson, W. Sean, Kussie, Paul, Lund-Katz, Sissel, Phillips, Michael C., Ghosh, Richik, Tall, Alan R.
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 12.05.1995; American Society for Biochemistry and Molecular Biology
• Subjects: Animals; Apolipoprotein A-I - isolation & purification; Apolipoprotein A-I - metabolism; Apolipoprotein A-I - ultrastructure; Carrier Proteins - isolation & purification; Carrier Proteins - metabolism; Carrier Proteins - ultrastructure; Cell Line; Cholesterol Ester Transfer Proteins; Cholesterol Esters - metabolism; Cricetinae; Cricetulus; Dimyristoylphosphatidylcholine; Glycoproteins; Humans; Kinetics; Lipoproteins, HDL - isolation & purification; Lipoproteins, HDL - metabolism; Lipoproteins, HDL - ultrastructure; Liposomes; Microscopy, Electron; Protein Conformation; Recombinant Proteins - isolation & purification; Recombinant Proteins - metabolism; Recombinant Proteins - ultrastructure; Spectrometry, Fluorescence; Transfection
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1074/jbc.270.19.11532

The plasma cholesteryl ester transfer protein (CETP) mediates the transfer of neutral lipids between lipoproteins and is associated with high density lipoproteins (HDL). To understand the mechanism of interaction of CETP with HDL, we studied the binding of pure recombinant CETP to l-palmitoyl-2-oleoylphosphatidylcho-line (POPC)/apoA-I discoidal particles. Separating bound from free CETP using native gradient gel electrophoresis, complexes of CETP with 10-nm hydrodynamic diameter discoidal particles migrated with a diameter of 12–16 nm, compared with ∼7.5 nm for CETP. At lower ratios of CETP to discs, CETP bound to discs without displacement of apoA-I. CETP alone was unable to generate discoidal complexes. Cross-linking and fluorescence resonance energy transfer experiments indicated that CETP bound to discs as monomers. Cross-linking of CETP to apoA-I in discs suggested proximity of apoA-I and CETP. By negative-stain electron microscopy, discoidal complexes containing CETP and CETP monoclonal antibody showed localization of antibody molecules to the disc edge, suggesting that CETP was bound to the disc edge. The binding of CETP to discs of different composition or size was studied. Discs (10-nm Stokes diameter) prepared with either apoA-I or apoA-II had a similar Kd (120 nm). Inclusion of 1 mol % cholesteryl oléate, 5 mol % cholesterol, or 6 mol % phosphatidylinositol increased the binding affinity of CETP 3–10 times (20–30 run). In comparison, plasma HDL3 had a Kd of ∼450 nM. For POPC/apoA-I discs, 10-nm discs bound CETP with much higher affinity than smaller 7.8-nm discs (Kd = 1–2 µm). 7.7-nm hydrodynamic diameter POPC/apoA-I spherical particles containing either triolein or cholesteryl oleate in their core bound CETP with higher affinity (Kd = 50–100 nm) than 7.8-nm POPC/apoA-I discs. Thus, CETP appears to bind to the perimeter of discoidal particles, possibly in a process in which flexible segments in apoA-I or apoA-II accommodate CETP at the disc edge. The binding of CETP to HDL is markedly influenced by overall particle size and shape and by lipid composition, and the increased binding affinity for cholesterol- and cholesteryl ester-containing discs suggests a higher affinity of CETP for nascent than mature HDL.