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Lipoproteins matrix

Phase I enzymes are located primarily in the endoplasmic reticulum of cells. These enzymes are membrane bound within a lipoprotein matrix and are referred to as microsomal enzymes. This is in reference to the subcellular fraction isolated by differential centrifugation of a liver homoge-... [Pg.7]

The cubic membrane in the apothecial cells is of special interest in many ways. It is not static, but reversible, and its appearance seems to be correlated with the development of the apothecium. It is believed to form de novo from an "amorphous lipoprotein matrix" [61]. This would indicate that true phase condensation could occur in some instances of the formation of cubic membranes. However, the interpretation presented [61] is, in view of our analysis, slightly inaccurate. In particular, it is incorrect to suppose that the development of the "lattice body" takes place through the formation and subsequent fusion of vesicles. The membranous "vesicles" are properly interpreted as sections normal to any lattice plane of the gyroid in which two axes are close to zero. It should be emphasised that similar images cm also be produced by projections of the D- and the P-PCS s. [Pg.286]

Most reviewers5 8 now argue that photosynthetic oxygen evolution results from a sequential four-step electron-transfer process in which oxidizing equivalents from chi fl+- are accumulated in a "charge-storing" complex to accomplish the concerted four-electron oxidation of two H2O molecules to one O2 molecule. The photooxidant (chi + ) and reductant (pheo O are one-electron transfer agents, and the matrix is the lipoprotein thylakoid membrane. Hence, evaluation and consideration of the one-electron redox potentials for PS 11 components within a lipoprotein matrix are necessary in order to assess the thermodynamic feasibility of proposed mechanistic sequences. [Pg.9]

Reelin is an extracellular matrix protein, which is secreted by neuronal cells and binds to two lipoprotein receptors (VLDLR and ApoER2) that relay the Reelin signal inside target neurons by docking the tyrosine kinase adapter disabled-1 (Dabl). This allows neurons to complete migration and adopt their ultimate positions in laminar structures in the central nervous system. In... [Pg.1063]

F9 embryonal carcinoma cells have a simple set of growth supplements which are required for growth in serum-free medium insulin, transferrin, and fibronectin (Rizzino and Sato, 1978). Fibronectin is a component of the extracellular matrix and facilitates the attachment of the cells to the culture dish. In addition, high density lipoprotein (HDL) has been observed to promote the growth of F9 cells serum-free. [Pg.473]

Although ribosomal proteins are readily observed as in Figures 13.7 and 13.8 altered matrix conditions can alter the relative ionization of bacterial whole-cell compounds. A systematic analysis involving laser power/fluence and sample preparation conditions reveals that if the concentrated trifluo-roacetic acid is added and the laser power increased above optimal conditions, ionization of bacterial surface compounds can be enhanced. Figure 13.9 is the resulting 9.4 T MALDI-FTMS, seen are both the Braun s lipoprotein56,57 and the Murein lipoprotein. Both of these compounds are complex combinations of hydrocarbon lipids attached to a protein base. This is the first MALDI-FTMS observation of surface proteins desorbed directly from whole cells by influencing ionization conditions. [Pg.291]

These data suggest that one of possible mechanisms of carotenoid delivery to the neural retina may involve lipoprotein uptake from the basal side of the RPE followed by its retro-endocytosis on the apical site (Lorenzi et al., 2008). Alternatively, the endocytosed lipoprotein may be degraded in the RPE followed by secretion of certain lipophilic components from the lipoprotein at the apical site. Due to low solubility of carotenoids in aqueous solutions, it may be suggested that they are secreted already bound to a protein or that an acceptor protein is available in the interphotoreceptor matrix and/or POS. [Pg.318]

Bachem, M.G., Wendelin, D., Schneiderhan, W., Haug, C., Zom, U., Gross, H.J., Schmid-Kotsas, A., and Gmnert, A., 1999, Depending on their concentration oxidized low density lipoproteins stimulate extracellular matrix synthesis or induce apoptosis in human coronary artery smooth muscle cells, Clin Chem Lab Med. 37 319-326. [Pg.141]

Heparin has been found to bind a large number of proteins (Table 3). The biological activity of heparin and related polysaccharides is usually ascribed to their interaction with heparin-binding proteins. These proteins can be classified into classes including (1) enzymes, (2) protease inhibitors, (3) lipoproteins, (4) growth factors, (5) chemokines, (6) selectins, (7) extracellular matrix proteins, (8) receptor proteins, (9) viral coat proteins, (10) nuclear proteins, and (11) other proteins (1). Many heparin-binding proteins are enzymes and enzyme inhibitors. For example, proteases in the coagulation cascade, such as factors Ha, IXa, Xa, Xlla, and Villa, are heparin-... [Pg.288]

The fat-soluble vitamins can be extracted from the food matrix without chemical change using a solvent system that is capable of effectively penetrating the tissues and breaking lipoprotein bonds. A total lipid extraction is required for the simultaneous determination of vitamers or vitamins with a wide range of polarities, and, for this purpose, a mixture of chloroform and methanol (2 + 1) is highly efficient (82). The Rose-Gottlieb method is particularly suitable for ex-... [Pg.340]

Sterol carrier protein 2 has also been shown to be involved in the intracellular transport and metabolism of cholesterol. Hirai et al. (1994) suggested that sterol carrier protein 2 plays an important role during foam cell formation induced by acetylated LDL and may be an important step in atherosclerosis [142], Lipoproteins can bind lipopolysaccharide and decrease the lipopoly-saccharide-stimulated production of proinflammatory cytokines [142, 143], In addition, lipoprotein entrapment by the extracellular matrix can lead to the progressive oxidation of LDL because of the action of lipoxygenases, reactive oxygen species, peroxynitrite, or myeloperoxidase [144, 145],... [Pg.96]


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See also in sourсe #XX -- [ Pg.583 ]




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