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Membranes intermediate components

Section 26 4 Phospholipids are intermediates in the biosynthesis of triacylglycerols from fatty acids and are the principal constituents of the lipid bilayer component of cell membranes... [Pg.1102]

Cholesterol is a widely distributed sterol found free or esterified to fatty acids. It is an important intermediate in the biosynthesis of steroid hormones and the principal component of cell plasma membranes and the membranes of intracellular organelles. [Pg.356]

Thus far, microtubules and actin filaments and their associated proteins have been discussed to advantage as independent cytoskeletal components. In actual fact, all of the components of the cytoskeleton (including intermediate filaments) are precisely integrated with one another (Langford, 1995), as well as with various cytoplasmic organelles, the nuclear membrane, the plasma membrane, and the extracellular matrix. In its totality the cytoskeleton subserves many coordinated and regulated functions in the cell ... [Pg.34]

A semi-permeable membrane, which is unequally permeable to different components and thus may show a potential difference across the membrane. In case (1), a diffusion potential occurs only if there is a difference in mobility between cation and anion. In case (2), we have to deal with the biologically important Donnan equilibrium e.g., a cell membrane may be permeable to small inorganic ions but impermeable to ions derived from high-molecular-weight proteins, so that across the membrane an osmotic pressure occurs in addition to a Donnan potential. The values concerned can be approximately calculated from the equations derived by Donnan35. In case (3), an intermediate situation, there is a combined effect of diffusion and the Donnan potential, so that its calculation becomes uncertain. [Pg.65]

The CP MAS NMR spectroscopy has been also extensively used for studies of proteins containing retinylidene chromophore like proteorhodopsin or bacteriorhodopsin. Bacteriorhodopsin is a protein component of purple membrane of Halobacterium salinarium.71 7 This protein contains 248 amino acids residues, forming a 7-helix bundle and a retinal chromophore covalently bound to Lys-216 via a Schiff base linkage. It is a light-driven proton pump that translocates protons from the inside to the outside of the cell. After photoisomerization of retinal, the reaction cycle is described by several intermediate states (J, K, L, M, N, O). Between L and M intermediate states, a proton transfer takes place from the protonated Schiff base to the anionic Asp85 at the central part of the protein. In the M and/or N intermediate states, the global conformational changes of the protein backbone take place. [Pg.158]

Figure 4.13. Model of peptide initiation of mast secretion. Insertion of the hydrophobic region of the peptide into the lipid bilayer properly orients the basic (+) groups at the N-terminus for binding to negatively charged membrane components. As a result, there is activation of the G protein complex with the subsequent generation of inositol triphosphate (IP ) and diacylglycerol (DAG). These intermediates then stimulate the mobilization of cellular Ca and possibly the transient influx of extracellular Ca as well as the activation ofprotein kinase C. As a consequence, the level of intracellular free ionized Ca is maintained at an elevated state. The end result is the exocytotic extrusion of secretory granules. Figure 4.13. Model of peptide initiation of mast secretion. Insertion of the hydrophobic region of the peptide into the lipid bilayer properly orients the basic (+) groups at the N-terminus for binding to negatively charged membrane components. As a result, there is activation of the G protein complex with the subsequent generation of inositol triphosphate (IP ) and diacylglycerol (DAG). These intermediates then stimulate the mobilization of cellular Ca and possibly the transient influx of extracellular Ca as well as the activation ofprotein kinase C. As a consequence, the level of intracellular free ionized Ca is maintained at an elevated state. The end result is the exocytotic extrusion of secretory granules.
The principal cytoskeletal proteins in non-muscle cells are actin, tubulin, and the components of intermediate filaments. Actin can exist either as monomers ( G-actin ) or polymerized into 70 A diameter double filament ( F-actin ). Polymerized actin usually is localized at the margins of the cells, linked by other proteins to the cell membrane. In contrast, tubulin forms hollow filaments, approximately 250 A in diameter, that are distributed within a cell in association, generally, with cell organelles. Stabilized microtubule structures are found in the flagella and cilia of eucaryotic cells however, in other instances - examples being the mitotic apparatus and the cytoskeletal elements arising in directed cell locomotion - the microtubules are temporal entities. Intermediate filaments, which are composed of keratin-like proteins, are approximately 100 A thick and form stable structural elements that impart rigidity, for example, to nerve axons and epithelial cells. [Pg.225]

The internal volume bounded by the plasma membrane, the cytoplasm (Fig. 1-3), is composed of an aqueous solution, the cytosol, and a variety of suspended particles with specific functions. The cytosol is a highly concentrated solution containing enzymes and the RNA molecules that encode them the components (amino acids and nucleotides) from which these macromolecules are assembled hundreds of small organic molecules called metabolites, intermediates in biosynthetic and degradative pathways coenzymes, compounds essential to many enzyme-catalyzed reactions inorganic ions and ribosomes, small particles (composed of protein and RNA molecules) that are the sites of protein synthesis. [Pg.3]


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