Physical and kinetic characterization of recombinant human cholesteryl ester transfer protein. 1996

D T Connolly, and J McIntyre, and D Heuvelman, and E E Remsen, and R E McKinnie, and L Vu, and M Melton, and R Monsell, and E S Krul, and K Glenn
Cardiovascular Diseases Research Department, Searie, St. Louis, Missouri 63167, USA.

Cholesteryl ester transfer protein (CETP) mediates the exchange of triglycerides (TGs), cholesteryl esters (CEs) and phospholipids (PLs) between lipoproteins in the plasma. In order to better understand the lipid transfer process, we have used recombinant human CETP expressed in cultured mammalian cells, purified to homogeneity by immunoaffinity chromatography. Purified recombinant CETP had a weight-average relative molecular mass (MW) of 69561, determined by sedimentation equilibrium, and a specific absorption coefficient of 0.83 litre.g-1.cm-1. The corresponding hydrodynamic diameter (Dh) of the protein, determined by dynamic light scattering, was 14 nm, which is nearly twice the expected value for a spheroidal protein of this molecular mass. These data suggest that CETP has a non-spheroidal shape in solution. The secondary structure of CETP was estimated by CD to contain 32% alpha-helix, 35% beta-sheet, 17% turn and 16% random coil. Like the natural protein from plasma, the recombinant protein consisted of several glycoforms that could be only partially deglycosylated using N-glycosidase F. Organic extraction of CETP followed by TLC showed that CE, unesterified cholesterol (UC), PL, TG and fatty acids (FA) were associated with the pure protein. Quantitative analyses verified that each mol of CETP contained 1.0 mol of cholesterol, 0.5 mol of TG and 1.3 mol of PL. CETP mediated the transfer of CE, TG, PL, and UC between lipoproteins, or between protein-free liposomes. In dual-label transfer experiments, the transfer rates for CE or TG from HDL to LDL were found to be proportional to the initial concentrations of the respective ligands in the donor HDL particles. Kinetic analysis of CE transfer was consistent with a carrier mechanism, having a Km of 700 nM for LDL particles and of 2000 nM for HDL particles, and a kcat of 2 s-1. The Km values were thus in the low range of the normal physiological concentration for each substrate. The carrier mechanism was verified independently for CE, TG, PL and UC in 'half-reaction' experiments.

UI MeSH Term Description Entries
D007700 Kinetics The rate dynamics in chemical or physical systems.
D008970 Molecular Weight The sum of the weight of all the atoms in a molecule. Molecular Weights,Weight, Molecular,Weights, Molecular
D011994 Recombinant Proteins Proteins prepared by recombinant DNA technology. Biosynthetic Protein,Biosynthetic Proteins,DNA Recombinant Proteins,Recombinant Protein,Proteins, Biosynthetic,Proteins, Recombinant DNA,DNA Proteins, Recombinant,Protein, Biosynthetic,Protein, Recombinant,Proteins, DNA Recombinant,Proteins, Recombinant,Recombinant DNA Proteins,Recombinant Proteins, DNA
D002352 Carrier Proteins Proteins that bind or transport specific substances in the blood, within the cell, or across cell membranes. Binding Proteins,Carrier Protein,Transport Protein,Transport Proteins,Binding Protein,Protein, Carrier,Proteins, Carrier
D002846 Chromatography, Affinity A chromatographic technique that utilizes the ability of biological molecules, often ANTIBODIES, to bind to certain ligands specifically and reversibly. It is used in protein biochemistry. (McGraw-Hill Dictionary of Scientific and Technical Terms, 4th ed) Chromatography, Bioaffinity,Immunochromatography,Affinity Chromatography,Bioaffinity Chromatography
D004591 Electrophoresis, Polyacrylamide Gel Electrophoresis in which a polyacrylamide gel is used as the diffusion medium. Polyacrylamide Gel Electrophoresis,SDS-PAGE,Sodium Dodecyl Sulfate-PAGE,Gel Electrophoresis, Polyacrylamide,SDS PAGE,Sodium Dodecyl Sulfate PAGE,Sodium Dodecyl Sulfate-PAGEs
D006023 Glycoproteins Conjugated protein-carbohydrate compounds including MUCINS; mucoid, and AMYLOID glycoproteins. C-Glycosylated Proteins,Glycosylated Protein,Glycosylated Proteins,N-Glycosylated Proteins,O-Glycosylated Proteins,Glycoprotein,Neoglycoproteins,Protein, Glycosylated,Proteins, C-Glycosylated,Proteins, Glycosylated,Proteins, N-Glycosylated,Proteins, O-Glycosylated
D006031 Glycosylation The synthetic chemistry reaction or enzymatic reaction of adding carbohydrate or glycosyl groups. GLYCOSYLTRANSFERASES carry out the enzymatic glycosylation reactions. The spontaneous, non-enzymatic attachment of reducing sugars to free amino groups in proteins, lipids, or nucleic acids is called GLYCATION (see MAILLARD REACTION). Protein Glycosylation,Glycosylation, Protein
D006224 Cricetinae A subfamily in the family MURIDAE, comprising the hamsters. Four of the more common genera are Cricetus, CRICETULUS; MESOCRICETUS; and PHODOPUS. Cricetus,Hamsters,Hamster
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man

Related Publications

D T Connolly, and J McIntyre, and D Heuvelman, and E E Remsen, and R E McKinnie, and L Vu, and M Melton, and R Monsell, and E S Krul, and K Glenn
February 1987, The Journal of biological chemistry,
D T Connolly, and J McIntyre, and D Heuvelman, and E E Remsen, and R E McKinnie, and L Vu, and M Melton, and R Monsell, and E S Krul, and K Glenn
July 1978, Proceedings of the National Academy of Sciences of the United States of America,
D T Connolly, and J McIntyre, and D Heuvelman, and E E Remsen, and R E McKinnie, and L Vu, and M Melton, and R Monsell, and E S Krul, and K Glenn
September 2010, Journal of lipid research,
D T Connolly, and J McIntyre, and D Heuvelman, and E E Remsen, and R E McKinnie, and L Vu, and M Melton, and R Monsell, and E S Krul, and K Glenn
September 1991, Lancet (London, England),
D T Connolly, and J McIntyre, and D Heuvelman, and E E Remsen, and R E McKinnie, and L Vu, and M Melton, and R Monsell, and E S Krul, and K Glenn
June 1999, Tanpakushitsu kakusan koso. Protein, nucleic acid, enzyme,
D T Connolly, and J McIntyre, and D Heuvelman, and E E Remsen, and R E McKinnie, and L Vu, and M Melton, and R Monsell, and E S Krul, and K Glenn
January 1992, International journal of clinical & laboratory research,
D T Connolly, and J McIntyre, and D Heuvelman, and E E Remsen, and R E McKinnie, and L Vu, and M Melton, and R Monsell, and E S Krul, and K Glenn
May 2023, Journal of chemical information and modeling,
D T Connolly, and J McIntyre, and D Heuvelman, and E E Remsen, and R E McKinnie, and L Vu, and M Melton, and R Monsell, and E S Krul, and K Glenn
January 1985, Methods in enzymology,
D T Connolly, and J McIntyre, and D Heuvelman, and E E Remsen, and R E McKinnie, and L Vu, and M Melton, and R Monsell, and E S Krul, and K Glenn
September 1999, Nihon rinsho. Japanese journal of clinical medicine,
D T Connolly, and J McIntyre, and D Heuvelman, and E E Remsen, and R E McKinnie, and L Vu, and M Melton, and R Monsell, and E S Krul, and K Glenn
August 1993, Journal of lipid research,
Copied contents to your clipboard!