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Channel formation

Fig. 5. NMOS capacitance voltage characteristics where C is the oxide capacitance, A shows low frequency characteristics, and B shows high frequency characteristics. At low frequencies C approaches C for negative voltages (accumulation) and positive voltages (inversion). In the flat-band (FB) condition there is no voltage difference between the semiconductor s surface and bulk. The threshold voltage, Dp for channel formation is the point where the... Fig. 5. NMOS capacitance voltage characteristics where C is the oxide capacitance, A shows low frequency characteristics, and B shows high frequency characteristics. At low frequencies C approaches C for negative voltages (accumulation) and positive voltages (inversion). In the flat-band (FB) condition there is no voltage difference between the semiconductor s surface and bulk. The threshold voltage, Dp for channel formation is the point where the...
Interestingly, certain other pore-forming toxins possess helix-bundle motifs that may participate in channel formation, in a manner similar to that proposed for colicin la. For example, the S-endotoxui produced by Bacillus thuringiensis is toxic to Coleoptera insects (beetles) and is composed of three domains, including a seven-helix bundle, a three-sheet domain, and a /3-sandwich. In the seven-helix bundle, helix 5 is highly hydrophobic, and the other six helices are amphipathic. In solution (Figure 10.32), the six amphipathic... [Pg.316]

O Connell, A. M. Koeppe, R. E., II Andersen, O. S., Kinetics of gramicidin channel formation in lipid bilayers Transmembrane monomer association, Science 250, 1256-1259 (1990). [Pg.280]

In electrochemistry similar phenomena are observed, for example, with the formation of insoluble films on electrodes or with ion selective channel formation in bilayer lipid membranes or nerve cell membranes (pages 377 and 458). [Pg.384]

Fig. 15. TOF spectra at = 34° for the 0(3P)+C2H4 reaction (Ec = 12.9kcalmol 1) recorded at (a) m/e = 14, (b) rri/e = 15, and (c) m/e = 42, using an electron energy of 17 eV. The fingerprints of all five energetically-allowed channels (formation of methylene, ketene, vinoxy, acetyl, and methyl) from the 0(3P) + C2H4 reaction are indicated (see text). Relative intensities at the TOF peak for m/e = 14, 15, and 42 are 0.23, 3.0, and 1, respectively. Fig. 15. TOF spectra at = 34° for the 0(3P)+C2H4 reaction (Ec = 12.9kcalmol 1) recorded at (a) m/e = 14, (b) rri/e = 15, and (c) m/e = 42, using an electron energy of 17 eV. The fingerprints of all five energetically-allowed channels (formation of methylene, ketene, vinoxy, acetyl, and methyl) from the 0(3P) + C2H4 reaction are indicated (see text). Relative intensities at the TOF peak for m/e = 14, 15, and 42 are 0.23, 3.0, and 1, respectively.
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]

Further evidence for microphase separahon has been seen by AFM. As expected, BPSH 00, with no ionic regions, displays no significant features in its AFM image. For BPSH 20, isolated ionic clusters have dimensions of 10-25 nm. These clusters are even more readily discerned from the non-ionic matrix in BPSH 40, but the domains appear to remain relatively segregated from each other. In the case of BPSH 50 and 60, connections between domains are clearly visible, especially in the case of the latter sample. It also should be noted, however, that these samples were in a dehydrated state. Therefore, it might be expected that even in the case of the lower acid content samples, it is likely that some channel formation between ionic domains will still occur upon the uptake of water. This can be clearly seen in its linear conductivity behavior as a function of disulfonated monomer (i.e., the percolation threshold has been reached by at least 20-30% content of disulfonated monomer). [Pg.145]

Blocker, D., Bachmeyer, C., Benz, R., Aktories, K. and Barth, H., Channel formation by the binding component of Clostridium botulinum C2 toxin glutamate 307 of C2II affects channel properties in vitro and pH-dependent C2I translocation in vivo, Biochem., 42, 5368-5377, 2003. [Pg.211]

Park B-N, Seo S, Evans PG (2007) Channel formation in single-monolayer pentacene thin film transistors. J Phys D 40 3506-3511... [Pg.234]

Amphotericin B (AmB) is a polyenic macrolide used in fungal infections and leishmaniasis, despite severe side effects (Figure 4.60). Fluorination of the macrolide skeleton has been performed using Selectfluor for F NMR studies on the mechanism of ion-channel formation in membranes by amphotericin B. ... [Pg.135]

Lavy T, Kaftory M (2007) Channels formation through photodimerization of guest molecules within solid inclusion compounds. CrystEngComm 9 123-127... [Pg.129]

In spite of the overwhelming importance of the channel mechanism for the transport of alkali and alkaline earth metal ions in biological systems, only carrier transport has been studied extensively by chemists. Studies on ion channel mimics of simple structures have long been limited to antibiotic families of gramicidin, amphotericin B, and others. Several pioneers have reported successful preparation of non-peptide artificial channels. However, their claims have been based on kinetic characteristics observed for the release of metal ions through liposomal membrane and lacked the very critical proofs of channel formation. Such a situation was... [Pg.164]

Figure 19. (A) Monensin modified channel forming unit 15, negatively charged a,(o-bifunctional amphiphile 16a and neutral one 16b, capable of forming monolayered membrane and positively charged bolaamphiphiles 17 as a sealing agent of the channel. (B) Model of channel formation by 15 in the monolayered membrane composed of 16 and the proposed blocking mode by 17." ... Figure 19. (A) Monensin modified channel forming unit 15, negatively charged a,(o-bifunctional amphiphile 16a and neutral one 16b, capable of forming monolayered membrane and positively charged bolaamphiphiles 17 as a sealing agent of the channel. (B) Model of channel formation by 15 in the monolayered membrane composed of 16 and the proposed blocking mode by 17." ...
Little is known at present on the process of channel formation and assembly. And even less on the regulation of channel formation. A very interesting and important question is how can two cells direct their hemichannels so that they fit each other forming the intercellular pore Research in this area is still at its beginning and many of the processes involved are not well understood. But nevertheless, in this chapter the present knowledge on the regulation of channel expression and turnover will be summarized. [Pg.63]

The reaction of CH3 with OH has two exit channels formation of the stabilized molecule CH3OH, or the product-formation reaction giving CH2OH + H. [Pg.441]

Copper has been employed commonly in relation with carbohydrates and aminoacids but other analytes can also be determined. Microalignment of the electrode with the channel outlet [89], deposition of a thin layer [81,108] or incorporation of a wire [21] are examples of in-channel formats. End-channel configurations such as those obtained by using a guide tube [11] or attaching a Cu wire perpendicularly to the outlet [32] after chip bonding were tested. Carbon nanotube (CNT)/copper composite electrodes have proved to be more sensitive, compared to the Cu and CNT alone, in the determination of carbohydrates [109]. [Pg.842]

Kawahara, M., and Kuroda, Y. (1997). [Molecular mechanism of neuronal death in Alzheimer s disease Ca(2+)-channel formation of beta amyloid protein molecules]. Tanpakushitsu Kakusan Koso 42, 2002-2010. [Pg.519]

All of the systems include a chromophore (photosensor or photoreceptor) that absorbs the light. The excitation of the photoreceptor is followed by a chemical reaction such as electron transfer, photoisomerization, ion channel formation, etc. [Pg.165]

How the hydrophilic a-LTX inserts into lipid membranes and makes cation-permeable pores is not fully known, but an in-depth insight into the mechanisms of channel formation has been gained by combining cryo-EM, biochemical and biophysical studies with toxin mutagenesis. a-LTX pore formation consists of at least three steps toxin tetramerisation, interaction with a specific cell-surface receptor and, finally, membrane insertion. Many experimental procedures can affect some of these steps and thereby prevent or assist channel formation. [Pg.179]

Although Ca2+ only carries a small proportion of currents through cell membrane-inserted a-LTX channels (Hurlbut et al. 1994 Tse and Tse 1999), the influx of Ca2+ through presynaptically-targeted a-LTX channels is most often referred to, because of the well-established link between presynaptic [Ca2+] and neurotransmitter release. There is a wealth of evidence indicating that in conditions favorable to channel formation (e.g., in the presence of divalent cations), influx of extracellular Ca2+ through a-LTX channels is an important aspect of a-LTX action. [Pg.182]

Hlubek MD, Stuenkel EL, Krasnoperov VG et al (2000) Calcium-independent receptor for a-latrotoxin and neurexin la facilitate toxin-induced channel formation evidence that channel formation results from tethering of toxin to membrane. Mol Pharmacol 57 519-28 Hurlbut WP, Ceccarelli B (1979) Use of black widow spider venom to study the release of neurotransmitters. Adv Cytopharmacol 3 87-115 87-115 Hurlbut WP, Chieregatti E, Valtorta F et al (1994) a-Latrotoxin channels in neuroblastoma cells. JMembr Biol 138 91-102... [Pg.201]

Carbon fiber electrodes ( 100 nm dia.) were also used to characterize the diffusion between adjacent stream zones at the interface between a micro fluidic system (16 channels 50 im wide, 57 im deep, separated by a 22- im wall) and a large volume using 10 mM ferrocyanide and amperometric detection [756]. It was reported that when the carbon fiber electrode was used in a PDMS chip, the in-channel format gave better peak symmetry than the end-channel format [757]. [Pg.217]

Reaven E., Leers-Sucheta S., Nomoto A. and Azhar S. (2001) Expression of scavenger receptor class B type 1 (SR-BI) promotes microvillar channel formation and selective cholesteryl ester transport in a heterologous reconstituted system. Proc. Natl. Acad. Sci. USA 98, 1613-1618. [Pg.440]


See other pages where Channel formation is mentioned: [Pg.246]    [Pg.316]    [Pg.317]    [Pg.555]    [Pg.401]    [Pg.460]    [Pg.7]    [Pg.210]    [Pg.398]    [Pg.145]    [Pg.250]    [Pg.571]    [Pg.180]    [Pg.311]    [Pg.14]    [Pg.64]    [Pg.65]    [Pg.246]    [Pg.143]    [Pg.329]    [Pg.835]    [Pg.839]    [Pg.604]    [Pg.181]    [Pg.202]   
See also in sourсe #XX -- [ Pg.107 ]




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