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Proteins composite

Process Rationale. The products of plasma fractionation must be both safe and efftcaceous, having an active component, protein composition, formulation, stabiUty, and dose form appropriate to the intended clinical appHcation. Processing must address a number of specific issues for each product. Different manufacturers may choose a different set or combination of unit operations for this purpose. [Pg.531]

Plant cell membranes are similar in overall structure and organization to animal cell membranes but differ in lipid and protein composition. [Pg.29]

Native biological membranes also display characteristic phase transitions, but these are broad and strongly dependent on the lipid and protein composition of the membrane. [Pg.269]

Figure 11.1. A flow-model scheme for treating the protein routing question. Labels refer to flow rates of carbon. The total carbon flux, into and out of the body, is 1, divided into F (for protein) and 1 - F for the remainder. The significant relevant internal fluxes are between the amino acid pool (coupled to the body protein pool), and the energy metabolism pool . The extent to which protein routing is observable in the body protein composition depends on the value ofX (See Fig. 11.2). Numbers in refer to suggested isotopic fractionations associated with a metabolic path, which are consistent with the data of the Ambrose and Norr (1993) and Tieszen and Fagre (1993) data set (see Section 4.1). Figure 11.1. A flow-model scheme for treating the protein routing question. Labels refer to flow rates of carbon. The total carbon flux, into and out of the body, is 1, divided into F (for protein) and 1 - F for the remainder. The significant relevant internal fluxes are between the amino acid pool (coupled to the body protein pool), and the energy metabolism pool . The extent to which protein routing is observable in the body protein composition depends on the value ofX (See Fig. 11.2). Numbers in refer to suggested isotopic fractionations associated with a metabolic path, which are consistent with the data of the Ambrose and Norr (1993) and Tieszen and Fagre (1993) data set (see Section 4.1).
Different Membranes Have Different Protein Compositions... [Pg.419]

The quality control of immunoglobuhns includes potency tests and conventional tests of safety and sterihty. The potency tests consist of neutrahzation tests that parallel those used for the potency assay of immunosera, except that in the cases of some immimoglobulins the assays are made in vitro, fit addition to the safety and sterihty tests, total protein is determined by nitrogen estimations, the protein composition by... [Pg.318]

Changes in cell-wall protein composition may regulate the molecular architecture of protein networks in a manner that allows new developmental outcomes for both fungal cell adhesion and root colonization. Further investigation of the structure and regulation of SRAP wall proteins will provide a more complete picture of their role in developing ectomycorrhizal tissues. Incompatibility between ectomycorrhizal hyphae and the host roots detected during the initial con-... [Pg.275]

For the work described below, only 600 pi (6 mg) of gland extract, obtained from the posterior gland, were available. The active protein was subsequently determined to be present at a concentration of about 0.5%, representing less than 100 pg (1 nmol) of hementin. The remainder of the extract consisted of several hundred inactive proteins and peptides. While the protein composition and cell types of the anterior and posterior glands are very different, the electrophoretic mobility of the active enzyme from... [Pg.257]

Silver white, relatively soft metal that is only applied in alloys. Oxygen and water attack pure Ca. The most prominent compound is the oxide (CaO) = burnt calcium, which hardens to calcium carbonate in mortar. Annual production of about 120 million tons. Burnt gypsum (CaS04 0.5 H20) hardens with water. A great step in evolution was the replacement of hard shells of brittle calcium carbonate by an internal skeleton of tough calcium phosphate (hydroxylapatite)-protein composite. Calcium is essential for all life forms. The daily requirement is 0.7-1.0 g. Humans (70 kg) contain 1 kg of calcium. Calcium silicate is the main component of cement. Marble is calcium carbonate in polycrystalline form and the favorite material of sculptors. [Pg.128]

Figure 3 A hydrophobic permeant must negotiate through a complex series of diffu-sional and thermodynamic barriers as it penetrates into a cell. The lipid and protein compositions and charge distribution of the inner and outer leaflets of the membrane lipid bilayer can play limiting roles, particularly at the tight junction. Depending upon the permeant s characteristics, it may remain within the plasma membrane or enter the cytoplasm, possibly in association with cytosolic proteins, and partition into cytoplasmic membranes. Figure 3 A hydrophobic permeant must negotiate through a complex series of diffu-sional and thermodynamic barriers as it penetrates into a cell. The lipid and protein compositions and charge distribution of the inner and outer leaflets of the membrane lipid bilayer can play limiting roles, particularly at the tight junction. Depending upon the permeant s characteristics, it may remain within the plasma membrane or enter the cytoplasm, possibly in association with cytosolic proteins, and partition into cytoplasmic membranes.
Anders E, Bagnell CR Jr, Krigman M, et al. 1982. Influence of dietary protein composition on lead absorption in rats. Bull Environ Contam Toxicol 28 61-67. [Pg.486]

Biological compartments Organic polymers (proteins) Composites Fats (membranes)... [Pg.106]

Peripheral and central nervous system myelin lipids are qualitatively similar. However, there are quantitative differences. PNS myelin has less cerebroside and sulfatide and considerably more sphingomyelin than CNS myelin. Of interest is the presence of the LM1 ganglioside, sialosyl-lactoneotetraosylceramide, as a characteristic component of myelin in the PNS of some species. These differences in lipid composition between CNS and PNS myelin are not, however, as dramatic as the differences in protein composition discussed below. [Pg.58]

The principal difference in the overall protein composition of PNS and CNS myelin is that P0 replaces PLP as the major protein, although myelin-forming Schwann cells do express very low levels of PLP. It is interesting to note that PLP and P0 proteins, which are so different in sequence, post-translational modifications and membrane topology, may have similar roles in the formation of structures as closely related as myelin of the CNS and PNS respectively. Expression of P0 in transfected cells results in cell-cell interactions that are due to homophilic binding... [Pg.63]

COPI-coated vesicles mediate intra-Golgi transport and Golgi to ER retrograde transport. The coats of these vesicles do not show the geometric forms seen with clathrin coats and have a more complex protein composition [3]. Coat protein purification first lead to the identification of a complex composed of seven individual coat-protein subunits, known as COPI or coatomer. Some of these subunits bear a sequence similarity to clathrin adaptors. In addition, there is a small GTP-binding protein, Arfl, present on COPI-coated vesicles. [Pg.142]

Oblinger, M. M., Brady, S. T., McQuarrie, I. G. and Lasek, R. Differences in the protein composition of the axonally transported cytoskeleton in peripheral and central mammalian neurons. /. Neurosci. 7 453-462,1987. [Pg.500]

Whole oilseeds and legumes and their derivatives (defatted flours, and protein concentrates and isolates) are used in traditional foods as sources of protein and for their texture-modifying functions. This article reviews, on a comparative basis, processes for preparation of vegetable food proteins, compositions and characteristics of the resulting food ingredients, and their functionalities and uses in traditional foods. [Pg.37]

Studies have been conducted for the intactness of biological fluids after photochemical treatment, in particular, proteins of allantoic fluid and blood semm, by methods of spectrophotometry and gel electrophoresis. The growth properties of semm were evaluated in cell culture. The protein composition of biological fluid was shown not to undergo dramatic changes during the course of photodynamic inactivation of vimses. [Pg.120]

Emission and excitation spectra were obtained for both natural and protease-liberated flavoprotein materials in 100 mM acetic acid. The Xmax for excitation was 330 for the natural and 410 nm for the protease-liberated flavoprotein while that for emission were 420 and 480 nm, respectively. These spectroscopic data show that these are flavoproteins and that the protein composition of natural and protease-liberated flavoprotein are somehow different. [Pg.376]


See other pages where Proteins composite is mentioned: [Pg.115]    [Pg.275]    [Pg.810]    [Pg.262]    [Pg.76]    [Pg.25]    [Pg.171]    [Pg.133]    [Pg.209]    [Pg.374]    [Pg.133]    [Pg.166]    [Pg.176]    [Pg.28]    [Pg.58]    [Pg.68]    [Pg.141]    [Pg.149]    [Pg.1616]    [Pg.63]    [Pg.127]    [Pg.168]    [Pg.133]    [Pg.769]    [Pg.1024]    [Pg.36]    [Pg.179]    [Pg.98]    [Pg.176]   
See also in sourсe #XX -- [ Pg.789 ]




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