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Translocation characterization

Hord NG, Perdew GH. 1994. Physio-chemical and immunochemical analysis of aryl hydrocarbon receptor nuclear translocator characterization oftwo monoclonal antibodies to the aryl hydrocarbon receptor nuclear translocator. Molec. Pharmacol. 46 618-24... [Pg.325]

The Na/K ATPase has been extensively purified and characterized, and consists of a catalytic a subunit of around 95 kDa and a glycoprotein 0 subunit of approximately 45 kDa (Skou, 1992). The functional transporter exists as a dimer with each monomer consisting of an a and /3 subunit. Hiatt aal. (1984) have su ested that the non-catalytic jS subunit may be involved in the cottect insertion of the a subunit into the lipid bilayer and, therefore, it is conceivable that a modification of the 0 subunit structure may be reflected by changes in the catalytic activity of the a subunit. Therefore, in studies involving the manipulation of tissue glutathione levels, alterations of intracellular redox state may have an effect on substrate binding at an extracellular site on this ion-translocating protein. [Pg.63]

The first purified and characterized drug substances were administered as aerosols as a topical treatment for asthma approximately 50 years ago. More recently, drugs have been evaluated for systemic delivery. For each category of drug the mechanism of clearance from the airways must be considered. These mechanisms may be listed as mucociliary transport, absorption, and cell-mediated translocation. The composition and residence time of the particle will influence the mechanism of clearance. [Pg.486]

Brandi, L., Fabbretti, A., Di Stefano, M., Lazzarini, A., Abbondi, M., and Gualerzi, C. O. (2006a). Characterization of GE82832, a peptide translocation inhibitor interacting with bacterial 30S ribosomal subunits, /v Al l 12, 1262—1270. [Pg.295]

The biogenesis of a gram-negative bacterial envelope requires subsequent sorting mechanisms for its component proteins after their translocation across the inner membrane (Duong et al., 1997 Danese and Silhavy, 1998). In addition, some proteins such as proteases and toxins are secreted through the outer membrane to the extracellular space. Three major secretion pathways have been characterized (Salmond and Reeves, 1993). [Pg.296]

Helicases catalyze the processive separation of duplex DNA into single strands. Despite sharing similarity to helicases, none of the chromatin remodelling factors, with the exception of the INO80 complex, have been shown to catalyze the separation of DNA strands (Shen et al, 2000). Instead, they can translocate on double-stranded (ds) DNA in an ATP-hydrolysis dependent manner and are characterized by their ability to generate superhelical torsional strain in DNA (Havas et al, 2000 Saha et al, 2002 Whitehouse et al, 2003). The crystal structure of Rad54, a member of the SWI/SNF family has been solved for both S. solfataricus and zebrafish which helps to understand the mechanism of the SWI/SNF ATPase domain in remodelling processes (Durr et al, 2005 Thoma et al, 2005). It reveals... [Pg.34]

Muller V, Aufurth S, Rahlfs S. 2001. The Na -cycle in Acetobacterium woodii identification and characterization of a Na -translocating FiFo-ATPase with a mixed oligomer of 8 and 16-kDa proteolipids. Biochim Biophys Acta 1505 108-20. [Pg.189]

The TP receptor requires the G/G protein to activate the Src-Ras-ERKl/2 (extracellular signal-regulated kinase 1 and 2) cascade to induce the proliferative response, which in turn promotes the rapid nuclear translocation of activated ERKl/2 (201). Because TP receptor may be activated by many inflammatory mediators (202-204), these findings suggest new therapeutic strategies that alter the ASM hypertrophy or hyperplasia observed in the chronic airflow obstruction and airway inflammation that characterizes asthma, chronic bronchitis, bronchiolitis obliterans, and chronic obstructive pulmonary disease. [Pg.156]

Transporters, particularly those carrying nonlipophilic species across biomembranes or model membranes, can be regarded as vectorial catalysts (and are also called carriers, translocators, permeases, pumps, and ports [e.g., symports and antiports]). Many specialized approaches and techniques have been developed to characterize such systems. This is reflected by the fact that there are currently twenty-three volumes in the Methods in Enzymology series (vols. 21,22,52-56,81,88,96-98,125-127,156-157, 171-174, and 191-192) devoted to biomembranes and their constituent proteins. Chapters in each of these volumes will be of interest to those investigating transport kinetics. Other volumes are devoted to ion channels (207), membrane fusion techniques (220 and 221), lipids (14, 35, 71, and 72), plant cell membranes (148), and a volume on the reconstitution of intracellular transport (219). See Ion Pumps... [Pg.448]


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See also in sourсe #XX -- [ Pg.208 , Pg.211 ]




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