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Plasma orientation

The plasma-oriented approach is also useful in estimating the interaction area between fast and slow charge carriers, by an appropriate adaptation of the concept of collision cross sections to electrolytes. As an illustration, the apparent cross-section radius of 181 nm in the case of a 0.005-mol dm solution subjected to a 1 mT magnetic field compares favorably with the 134 nm computed from the classical Rosenbluth formula applying to electron-ion collisions. [Pg.346]

She et al. [128] used rolling contact to estimate the adhesion hysteresis at polymer/oxide interfaces. By plasma oxidation of the cylinders of crosslinked PDMS, silica-like surfaces were generated which could hydrogen bond to PDMS r olecules. In contrast to unmodified surfaces, the adhesion hysteresis was shown to be larger and proportional to the molecular weight of grafted polymer on the substrate. The observed hysteresis was interpreted in terms of the orientation and relaxation of polymer chains known as Lake-Thomas effect. [Pg.133]

Figure 46-8. Fusion of a vesicle with the plasma membrane preserves the orientation of any integral proteins embedded in the vesicle bilayer. Initially, the amino terminal of the protein faces the lumen, or inner cavity, of such a vesicle. After fusion, the amino terminal is on the exterior surface of the plasma membrane. That the orientation of the protein has not been reversed can be perceived by noting that the other end of the molecule, the carboxyl terminal, is always immersed in the cytoplasm. The lumen of a vesicle and the outside of the cell are topologically equivalent. (Re drawn and modified, with permission, from Lodish HF, Rothman JE The assembly of cell membranes. Sci Am [Jan] 1979 240 43.)... Figure 46-8. Fusion of a vesicle with the plasma membrane preserves the orientation of any integral proteins embedded in the vesicle bilayer. Initially, the amino terminal of the protein faces the lumen, or inner cavity, of such a vesicle. After fusion, the amino terminal is on the exterior surface of the plasma membrane. That the orientation of the protein has not been reversed can be perceived by noting that the other end of the molecule, the carboxyl terminal, is always immersed in the cytoplasm. The lumen of a vesicle and the outside of the cell are topologically equivalent. (Re drawn and modified, with permission, from Lodish HF, Rothman JE The assembly of cell membranes. Sci Am [Jan] 1979 240 43.)...
Figure 8.6 Horizontal axially viewed torch and vertically oriented, radially viewed plasma configuration. Reproduced by permission of Varian, Inc. Figure 8.6 Horizontal axially viewed torch and vertically oriented, radially viewed plasma configuration. Reproduced by permission of Varian, Inc.
The determination of theophylline in plasma can also be accomplished by various immunoassay techniques.66-67 Theophylline was also determined by a polarization fluoroimmunoassays but found to have a caffeine interference.88. In a more research oriented application, the interaction of caffeine with L-tryptophan was studied using h NMR with the results indicating that caffeine interacted with tryptophan in a 1 1 molar ratio through parallel stacking.69... [Pg.39]

Because there are no sarcomeres in smooth muscle, there are no Z lines. Instead, the actin filaments are attached to dense bodies. These structures, which contain the same protein as Z lines, are positioned throughout the cytoplasm of the smooth muscle cell as well as attached to the internal surface of the plasma membrane. Myosin filaments are associated with the actin filaments, forming contractile bundles oriented in a diagonal manner. This arrangement forms a diamond-shaped lattice of contractile elements throughout the cytoplasm. Consequently, the interaction of actin and myosin during contraction causes the cell to become shorter and wider. [Pg.157]

Figure 5.10 Ribbon diagram of the transferrin receptor dimer depicted in its likely orientation with regard to the plasma membrane. One monomer is blue, the other is coloured according to domain the protease-like, apical and helical domains are red, green and yellow respectively the stalk is shown in grey, connected to the putative membrane spanning helices in black. Pink spheres indicate the location of Sm3+ ions. Reprinted with permission from Lawrence et ah, 1999. Copyright (1999) American Association for the Advancement of Science. Figure 5.10 Ribbon diagram of the transferrin receptor dimer depicted in its likely orientation with regard to the plasma membrane. One monomer is blue, the other is coloured according to domain the protease-like, apical and helical domains are red, green and yellow respectively the stalk is shown in grey, connected to the putative membrane spanning helices in black. Pink spheres indicate the location of Sm3+ ions. Reprinted with permission from Lawrence et ah, 1999. Copyright (1999) American Association for the Advancement of Science.
The equivalent of the tryptic fragment of human transferrin receptor has been expressed in Chinese hamster ovary cells and its structure determined at a resolution of 0.32 nm (Lawrence et ah, 1999). The asymmetric unit of the crystals contains four transferrin receptor dimers. Interpretable electron density is found for the entire tryptic fragment except for Arg-121 at the amino terminus, and density is also seen for the first N-acetylglucosamine residue at each of the N-glycosylation sites. The transferrin receptor monomer is made up of three distinct domains, organized such that the dimer is butterfly shaped (Figure 5.10, Plate 7). The likely orientation of the dimer with respect to the plasma membrane has been assigned on the basis of the... [Pg.157]

Fig. 18. Hypothetical orientation of the flavin photoreceptor within the plasma-lemma in cells of Funaria leaves202, based on known angles of flavin transition vectors in the blue105)... Fig. 18. Hypothetical orientation of the flavin photoreceptor within the plasma-lemma in cells of Funaria leaves202, based on known angles of flavin transition vectors in the blue105)...
H. Wang, Y. Liu, Y. Yang, T. Deng, G.L. Shen, and R.Q. Yu, A protein A-based orientation-control-led immobilization strategy for antibodies using nanometer-sized gold particles and plasma-polymerized film. Anal. Biochem. 324, 219-226 (2004). [Pg.278]

Although the main thrust of future crystallographic work must be oriented towards a higher resolution structure, many further experiments can be envisaged which should help to probe structure-function relationships and physiological roles for hCP in the plasma. Such experiments include ... [Pg.84]

Optical guiding in preformed plasmas has been extensively investigated in experiments mainly oriented to demonstrate the production of relativistic electrons in LWF-related schemes. Plasma channel formation has been pursued with a variety of means, ranging from the use of hydrodynamic and shock-wave... [Pg.147]

FIG. 5. View of the SR network in a longitudinally oriented rabbit portal vein smooth muscle cell stained with osmium ferricyanide. Note the close apposition of the SR to the plasma membrane (small arrows) and caveolae, as well as its relationship to mitochondria (M) in some instances the SR completely surrounds mitochondria. [Pg.263]

Shibaoka H. Plant hormone-induced changes in the orientation of cortical microtubules alterations in the cross-linking between microtubules and the plasma membrane. Ann Rev Plant Physiol Mol Biol 1994 45 527-544. [Pg.34]


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See also in sourсe #XX -- [ Pg.81 ]




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