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Lipids complementary

Biomolecules interact with one another through molecular surfaces that are structurally complementary. How can various proteins interact with molecules as different as simple ions, hydrophobic lipids, polar but uncharged carbohydrates, and even nucleic acids ... [Pg.32]

Ascorbic acid and alpha-tocopherol are effective blocking agents against N-nitroso compound formation. Ascorbic acid is effective particularly in aqueous media, and tocopherol effective particularly in lipid phases. They should be used in conjunction due to the mutually complementary actions of the two vitamins in blocking nitrosamine formation in both aqueous and lipid media. [Pg.201]

Although most of the analytical studies focused on lipid substances encountered in archaeological objects and museum works of art are carried out using separation techniques, direct mass spectrometry represents an alternative or a complementary analytical way for identifying such complex materials. [Pg.126]

Hence, direct mass spectrometry techniques, either using El or ESI, appear to be powerful and innovative analytical tools for elucidating the structure of the main biomarkers present in a wide range of waxes and lipids that may be preserved in archaeological objects and in museum works of art. In most cases, they have nevertheless to be cautiously exploited in combination with other complementary analytical techniques. [Pg.126]

Corr, L. T., Richards, M. P., Jim, S., Ambrose, S. H., Mackie, A., Beattie, O. and Evershed, R. P. (2008) Probing dietary change of the Kwad y Dan Ts inchj individual, an ancient glacier body from British Columbia I. Complementary use of marine lipid biomarker and carbon... [Pg.425]

Fig. 8 Immobilization of urokinase on the surfaces of islet cells, (a) Surface modification (/) chemical structure of ssDNA-PEG-lipid, and (2) ssDNA-PEG-lipid anchoring to the cell membrane. (b) Introduction of a complementary ssDNA onto urokinase, which was first modified with a madeimide group by a cross-linker, EMCS. (c) Urokinase-immobilization through DNA... Fig. 8 Immobilization of urokinase on the surfaces of islet cells, (a) Surface modification (/) chemical structure of ssDNA-PEG-lipid, and (2) ssDNA-PEG-lipid anchoring to the cell membrane. (b) Introduction of a complementary ssDNA onto urokinase, which was first modified with a madeimide group by a cross-linker, EMCS. (c) Urokinase-immobilization through DNA...
From the density profiles one cannot really judge the effect of the double bonds the density profiles for membranes of saturated lipids are very similar to those of unsaturated ones. Therefore it is necessary to consider some of the conformational characteristics of the tails. It is possible to compute the order parameter profile for both the saturated and the unsaturated chains. The order parameter profile for the saturated chain closely follows the results presented in Figure 17 for DMPC membranes for both the SCF and the MD predictions. The order parameter profiles for the unsaturated chain closely follows the MC predictions, as discussed in Figure 9. A pronounced dip is found near the cis double bond. For this reason, we choose here to present complementary data about the conformational properties of the acyl chains. [Pg.72]

To confirm that the effects of NO on O2 consumption are due to inhibition of hpid peroxidation, we also examined the effect of NO on TBARS, a product of lipid peroxidation. Cells were oxidized by Fe ", and 0.9 (jM N0 was added 1 min later. Cells were collected after 5 min for assay. Figure 5 shows that Fe " increased lipid peroxidation, and NO inhibited it by 63% (after subtracting basal levels). It is noteworthy that the percentage inhibition of O2 uptake by NO as measured by the change in O2 concentration under similar conditions was similar (78%) lending verification to these complementary methods. These results confirm the relationship of O2 consumption and lipid peroxidation in these experiments... [Pg.104]

Transmission electron microscopy (TEM) can provide valuable information on particle size, shape, and structure, as well as on the presence of different types of colloidal structures within the dispersion. As a complication, however, all electron microscopic techniques applicable for solid lipid nanoparticles require more or less sophisticated specimen preparation procedures that may lead to artifacts. Considerable experience is often necessary to distinguish these artifacts from real structures and to decide whether the structures observed are representative of the sample. Moreover, most TEM techniques can give only a two-dimensional projection of the three-dimensional objects under investigation. Because it may be difficult to conclude the shape of the original object from electron micrographs, additional information derived from complementary characterization methods is often very helpful for the interpretation of electron microscopic data. [Pg.13]

The above data suggest that a crosslinked bilayer vesicle is essentially a single polymer molecule (really two, one in each half of the bilayer). In other words the polymerization of the lipid monomers exceeded a gel-point. This concept raises the question of what mole fraction of bis-substituted lipid is necessary to achieve a gel-point for a bilayer composed of a crosslinker lipid, i.e. bis-lipid, and a mono-substituted lipid. Approximately 30% of the lipids in a bilayer vesicle of SorbPCs must be bis-SorbPC (4) in order to produce a polymerized vesicle that could not be dissolved by detergent or organic solvent [29], A complementary study of Kolchens et al. found that the lateral diffusion coefficient, D, of a small nonreactive lipid probe in a polymerized bilayer of mono- and bis-AcrylPC was dramatically reduced when the mole fraction of the bis-AcrylPC, was increased from 0.3 to 0.4 [24]. The decreased freedom of motion of the probe molecule indicates the onset of a crosslinked bilayer in a manner consistent with a 2-dimensional gel-point. [Pg.59]

Complementary Surfactants other proteins, polysaccharides not lipids. [Pg.151]

Some time after the evolution of this primitive protein-synthesizing system, there was a further development DNA molecules with sequences complementary to the self-replicating RNA molecules took over the function of conserving the genetic information, and RNA molecules evolved to play roles in protein synthesis. (We explain in Chapter 8 why DNA is a more stable molecule than RNA and thus a better repository of inheritable information.) Proteins proved to be versatile catalysts and, over time, took over that function. Lipidlike compounds in the primordial soup formed relatively impermeable layers around self-replicating collections of molecules. The concentration of proteins and nucleic acids within these lipid enclosures favored the molecular interactions required in self-replication. [Pg.33]

Two complementary experiments show that the orientation and hiding of one or the other face of the steroid ring of cholate can occur when mixtures of lecithin and bile salt are considered. One of these experiments was performed by Etienne (4), who observed the following facts incidentally while extracting lipids from the serum lipoproteins by Delsal s method. This method utilizes a mixture of methanol and methylal (1 to 4) in the cold. The proteins are precipitated, while the lipids are dissolved in the methanol-methylal solvent mixture. If this solution of the lipids is evaporated, the residue is soluble in nonpolar solvents, such as chloroform. However, if sodium cholate is added to the lipoproteins before their extraction, the residue obtained after the methylal-methanol solvent evaporates is insoluble in chloroform. More precisely, while cholesterol and the triglycerides of the lipidic residue are extracted by chloroform, all of the lecithin remains insoluble, associated to the bile salt. The explanation is probably as follows. During evaporation, methylal with its low boiling point (44°C.), evaporates first, and the solvent becomes more and more concentrated with methanol and the residual water from the lipoprotein aqueous solution. Therefore, in the lecithin plus... [Pg.86]

We believe that the type of investigations that are outlined briefly above provide interesting new information on the properties of lipids from both technical and biophysical points of view. Measurements on electrolyte-lipid semiconductor systems should provide useful information complementary to that obtained from BLM investigations. Furthermore, the gas sensitivity of the electrical properties of lipids could be utilized in practical devices. [Pg.72]


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See also in sourсe #XX -- [ Pg.140 , Pg.141 , Pg.143 ]




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Complementariness

Complementary

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