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  • Chemistry  (3)
  • diffusion coefficient  (1)
  • 1995-1999  (4)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of muscle research and cell motility 20 (1999), S. 199-209 
    ISSN: 1573-2657
    Keywords: concentration ; diffusion coefficient ; frog ; muscle ; parvalbumin ; water
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract The concentrations and diffusivity of two isoforms of parvalbumin, IVa and IVb, were measured using quantitative SDS PAGE in single fibers from semitendinosus muscles of the frog Rana temporaria. The concentrations of IVa and IVb were 2.9 ± 0.3 (SEM) and 4.5 ± 0.5 gl−1 total fiber volume, respectively. The total concentration of parvalbumin (7.4 ± 0.8 gl−1 total fiber) corresponds to a cytosolic concentration of 0.9 ± 0.1 mmoll−1 myoplasmic water. Estimates for the transverse and longitudinal diffusion coefficients for parvalbumin at 4°C were obtained in two ways: (1) by diffusion of parvalbumin out of skinned fibers into droplets of relaxing solution, and (2) by diffusion of parvalbumin between two juxtaposed skinned fibers under oil. The transverse diffusion coefficient obtained using the droplet method was significantly lower than that obtained using juxtaposed fibers, but the longitudinal diffusion coefficients obtained from both methods were similar. The juxtaposed fiber method more accurately approximates parvalbumin diffusion in undisturbed myoplasm because no artificial solutions were used and, upon fiber-to-fiber contact, a potentially confounding oil barrier at the interface rapidly disperses. The juxtaposed fiber method yielded values for transverse (4.27 ± 0.87 × 10−7 cm2 s−1) and longitudinal (3.20 ± 0.74 × 10−7 cm2 s−1) diffusion coefficients that were not significantly different, suggesting that diffusion of parvalbumin in myoplasm is essentially isotropic. The average diffusion coefficient of frog parvalbumin in myoplasm (3.74 ± 0.81 × 10−7 cm2 s−1; 4°C) is approximately a third of that estimated for frog parvalbumin diffusing in bulk water into and out of 3% agarose cylinders (10.6 × 10−7 cm2 s−1; 4°C). The reduced translational mobility of parvalbumin in myoplasm reflects an elevated effective viscosity due to tortuosity and viscous drag imposed by the fixed proteins of the cytomatrix and the numerous diffusible particles of the cytosol.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Macromolecular Chemistry and Physics 199 (1998), S. 2777-2783 
    ISSN: 1022-1352
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The synthesis and characterization of Cell-SAc 3, a cellulose isopentyl (IP) ether with additional pendant S-acetyl (SAc) moieties (degree of substitution DSIP = 2.5, DSSAc = 0.4) are reported. Cell-SAc forms stable monolayers at the air-water interface once spread from dilute chloroform solution. The pressure-area isotherm of Cell-SAc is nearly identical to the parent Cell-IP 1, both exhibiting an expanded liquid phase at surface areas of 70 and 67 Å, respectively. The similarity of the two isotherms shows that the presence of the S-acetyl substituent does not result in an increase in the molecular area, at which the liquid-crystal analogous phase occurs. This observation suggests that the side-chains with the pendant S-acetyl group are oriented away from the water surface. Monolayers of Cell-SAc can be efficiently transferred onto silicon and hydrophobized glass or quartz substrates by a downstroke and upstroke technique. Resulting multilayers were characterized using X-ray reflection, FTIR, and UV-vis spectroscopy. The presence of S-acetyl moieties was found to increase the monolayer thickness relative to the parent Cell-IP. The cleavage of the S-acetyl group within the LB film is reported.
    Additional Material: 5 Ill.
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  • 3
    ISSN: 1022-1352
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A new photocrosslinkable polymer designed for application in second harmonic generation has been prepared and tested for frequency doubling of IR lasers. The polymer is based on a colorless polyurethane with pendant tolane nonlinear optical chromophores that carry a polymerizable styrene moiety at their extremities. Photocrosslinking is achieved by irradiation of films containing a small amount of a bleachable radical photoinitiator. The effect of photoinduced radical crosslinking on the mobility of the chromophores has been studied by recording the intensity of the frequency doubled light, generated by a poled sample, with increasing temperature. As expected, photocrosslinking leads to NLO materials with highly stable chromophore orientation.
    Additional Material: 4 Ill.
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  • 4
    ISSN: 1434-193X
    Keywords: Phenyleneethynylene ; Oligomers ; Alkynes ; Protective groups ; Repetitive synthesis ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: -Monodisperse oligo(para-phenyleneethynylene)s (oligoPPEs) were synthesized by a divergent-convergent synthesis starting from 1,4-dihexyl-2-(3-hydroxyprop-1-ynyl)-5-[2-(triisopropylsilyl)ethynyl]benzene and using the Pd/Cu-catalyzed alkyne-aryl coupling. The groups hydroxymethyl (HOM) and triisopropylsilyl (TIPS) function as orthogonal protective groups for the acetylene moieties. The polar HOM group shows a strong impact on the chromatographic behaviour of the products and makes the isolation of pure compounds very easy. The synthesis was pursued up to the nonamer. The oligoPPEs were fully characterised, including absorption and emission spectral data.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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