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Proto-membrane

Exposure time of proto-membrane before precipitation. The effect of exposure to atmosphere before immersion is dependent on the solvent property (e.g., volatility, water absorption) and atmosphere property (e.g., temperature, humidity). This step (i.e., combination of EIPS or VIPS with NIPS cf. above) has significant effects on the characteristics of the skin layer and the degree of anisotropy of the resulting membrane [14]. [Pg.30]

Interphasic molecule or system of molecules. Proto-membrane... [Pg.438]

The solution is cast into a film of 100-500 xm thickness (known as the proto-membrane). [Pg.8]

Membranes have many functions in addition to acting as a container for the macromolecular polymers of life. Three primary membrane functions associated with a proto cell would include selective inward transport of nutrients from the environment, capture of the energy available in light or oxidation-reduction potentials, and coupling of that energy to some form of energy currency such as ATP in order to drive polymer synthesis (Fig. 3). [Pg.11]

T. Cavalier-Smith (2001). Obcells as proto-organisms membrane heredity, lithophosphorylation, and the origins of the genetic code, the first cells, and photosynthesis. J. Mol. Evol., 53, 555-595. [Pg.217]

Methylation has also been found to enhance the membrane affinity of a number of different Icmt substrates. Of particular interest has been the effect of methylation on the biology of the proto-oncoprotein Ras. In an early study, K-Ras produced by in vitro translation was found to be farne-sylated, but further modification including proteolysis and methylation required incubation with intracellular membranes. Unmethylated K-Ras produced by in vitro translation in the presence of pancreatic microsomes and an inhibitor of methylation, methylthioadenosine (MTA), was found to associate less efficiently with PlOO membrane fractions from COS cells than the fully modified protein [55]. In other in vitro studies, farnesylated peptides corresponding to the C-terminus of Ras had 20-fold higher affinity for liposomes when methylated [56]. [Pg.79]

In general, cilia are widespread finger-like cell appendages. The structure of a proto-typic motile cilium is characterized as follows the ciliary shaft originates from a basal body complex in the apical cytoplasm beneath the plasma membrane (Figure 2A). [Pg.212]

A complex multi-chromophoric system comprises the purple membrane patches from Halobacterium salinarium. These patches are composed of about 3000 bacter-iorhodopsin proteins. The hyperpolarizability of solubilized monomeric bacterio-rhodopsin was measured by HRS and found to be 2100 x 10 esu at 1064 nm. This high value is due to the presence of a chromophore in the protein, the proto-nated Schiff base of retinal. A purple membrane patch can be treated as a two-dimensional crystal of bacteriorhodopsin proteins, and its structure is known in considerable detail. The analysis of the purple membrane tensor was performed by adding the hyperpolarizabilities of the individual proteins in the purple membrane. From (depolarized) HRS measurements on purple membrane suspensions, the structure of the purple membrane patches, and an average membrane size measured by atomic force microscopy, a fi value of 2200 x 10 esu was calculated for bacteriorhodopsin [22]. The organization of the dipolar protonated Schiff base chro-mophores in the membranes was found to be predominantly octopolar. [Pg.3438]

Many reactions over zeolites don t seem to require strong acidity. They are probably utilizing the polarity of the crystal lattice, and taking advantage of the tremendous reactant-concentrating effect of the vast, membrane-like internal surface area of the zeolite. Perhaps we even can look at zeolites as rugged, primitive proto-enzymes. Of course, they... [Pg.280]

Evidence for the link between PKC activation and cell proliferation was initially provided by the demonstration that two intracellular events associated with cell replication - a rise in cytosolic pH and the expression of the proto-oncogenes c-fi/s and c-tnyc - are controlled by PKC PKC stimulates the membrane bound Na /H exchange mechanism in smooth muscle which extrudes intracellular H in exchange for extracellular Na this leads to a rise in intracellular pH, a prerequisite for cellular DNA replication (Mitsuka and Berk, 1991). c-fbs and c-myc are proto-oncogenes whose transcription to mRNA is one of the earliest markers of cell proliferation they encode for proteins, found in the cell nucleus, which initiate the sequence of events leading to DNA synthesis (Rozen-gurt, 1991). [Pg.181]

J. Mosig, Dreidimensionale mathematische Modellierung einer Brennstoffzelle unit Proto-nen-Austausche Membran (PEMFC) PhD thesis, Forschungszentrum Julich, Jtil-3480 D82, ISSN 0944-2952,1997. [Pg.541]

Photocyclisation - A wide variety of ring-forming reactions has again been reported. Irradiation of azepine derivative (16) results in 4-n-electrocyclisation to a mixture of the corresponding exo and endo cyclobutenes.6-Ti-Electrocyclisa-tion has been employed in a scaled-up synthesis (>300g) of 6-aza-l,10-phenan-throic anhydride (18) from the stilbazole (17). f-Azobenzene, incorporated into water-swollen acid-form Nafion fluorocarbon membranes, exists as the proto-nated form (19) and exhibits ambient temperature fluorescence, previously... [Pg.242]

Polypeptides that have these C-terminal modifications include the ras proto-oncogene proteins and many of their small G-protein analogs, the y-subunits of the large G-proteins, and the retinal cGMP phosphodiesterase (Clarke, 1992). These proteins are all involved in the transduction of information from the exterior environment of a cell to its interior. The modification of these proteins can allow for specific interactions with the membrane bilayer or with specific receptor proteins on the plasma membrane or internal membrane systems. The specific role of the C-terminal methylation reaction has been tested recently in the yeast system. [Pg.291]


See other pages where Proto-membrane is mentioned: [Pg.27]    [Pg.28]    [Pg.27]    [Pg.28]    [Pg.44]    [Pg.488]    [Pg.259]    [Pg.219]    [Pg.6]    [Pg.342]    [Pg.40]    [Pg.49]    [Pg.183]    [Pg.107]    [Pg.32]    [Pg.173]    [Pg.332]    [Pg.572]    [Pg.1564]    [Pg.857]    [Pg.20]    [Pg.43]    [Pg.71]    [Pg.198]    [Pg.59]    [Pg.337]    [Pg.49]    [Pg.160]    [Pg.46]    [Pg.68]    [Pg.173]    [Pg.572]    [Pg.1241]    [Pg.215]    [Pg.782]    [Pg.83]    [Pg.229]    [Pg.886]   
See also in sourсe #XX -- [ Pg.27 , Pg.30 ]

See also in sourсe #XX -- [ Pg.438 ]




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