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  • 1
    ISSN: 0006-3525
    Keywords: melittin ; dansylcadaverine-melittin ; dansylcadaverine-substance P ; peptide-lipid interaction ; thermodynamic treatment ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A thermodynamic approach is proposed to quantitatively analyze the binding isotherms of peptides to model membranes as a function of one adjustable parameter, the actual peptide charge in solution zp+. The main features of this approach are a theoretical expression for the partition coefficient calculated from the molar free energies of the peptide in the aqueous and lipid phases, an equation proposed by S. Stankowski [(1991) Biophysical Journal, Vol. 60, p. 341] to evaluate the activity coefficient of the peptide in the lipid phase, and the Debye-Hückle equation that quantifies the activity coefficient of the peptide in the aqueous phase. To assess the validity of this approach we have studied, by means of steady-state fluorescence spectroscopy, the interaction of basic amphipathic peptides such as melittin and its dansylcadaverine analogue (DNC-melittin), as well as a new fluorescent analogue of substance P, SP (DNC-SP) with neutral phospholipid membranes. A consistent quantitative analysis of each binding curve was achieved. The zp+ values obtained were always found to be lower than the physical charge of the peptide. These zp+ values can be rationalized by considering that the peptide charged groups are strongly associated with counterions in buffer solution at a given ionic strength. The partition coefficients theoretically derived using the zp+ values were in agreement with those deduced from the Gouy-Chapman formalism. Ultimately, from the zp+ values the molar free energies for the free and lipid-bound states of the peptides have been calculated. © 1997 John Wiley & Sons, Inc. Biopoly 42: 169-181, 1997
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 189 (1988), S. 1657-1669 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Deviations in the determination of the unperturbed dimensions of polymers arising in ternary polymer systems (solvent (1)/solvent (2)/polymer) can be explained by the inaccurate use of an interaction parameter independent of polymer molecular weight. On this basis, a new formalism for the calculation of the second virial coefficient from intrinsic viscosity is proposed. This formalism was tested (and compared with well established formalisms) for all ternary polymer systems with simultaneous intrinsic viscosity and second virial coefficient data in the literature.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 188 (1987), S. 2909-2920 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The intrinsic viscosities, [η], for the ternary systems alkane (1)/2-butanone (2)/poly(dimethylsiloxane) (PDMS)(3), with the alkanes decane, dodecane and hexadecane, are determined at 20,0°C. The constants a of the Mark-Houwink equation and the constant of the unperturbed dimensions, KΘ, of the polymer are evaluated over the whole composition range of the binary solvent mixture. [η] shows a pronounced maximum at intermediate compositions as found in cosolvent mixtures. In these cosolvent mixtures, the numerical values of KΘ are higher than in the single-component solvents, because the cosolvent mixtures correspond to a mixed solvent with an excess free energy, GE ≥ 0, the increase in KΘ being only moderate though. A new procedure taking into account ternary interactions, to evaluate the intrinsic viscosity in ternary systems from GE values is proposed. The influence of ternary interactions through a constant (1-2aχ) is also investigated. From these new expressions the constant of the apparent polymer unperturbed dimensions, K*Θ, and (1-2aχ) are calculated and compared with those directly evaluated from second virial coefficients.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 189 (1988), S. 1643-1656 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The unperturbed dimensions parameter KΘ is one of the most important characteristics of a polymer chain. For binary systems (polymer/solvent) and mostly for ternary systems (polymer/solvent(1)/solvent(2)) the KΘ values show large discrepancies with respect to those under thetaconditions in a single solvent. These discrepancies can be explained by considering that the interaction parameter χ (and consequently the coil dimensions or the number of intramolecular contacts between polymer segments) changes with molecular weight M. Assuming this dependency, a modified Stockmayer-Fixman equation is proposed from which a unique value of KΘ for a given polymer, independent of M, is obtained. The use for ternary polymer systems of an interaction parameter between polymer and the solvent mixture (χ3M) which depends on M, allows to calculate a single KΘ value for a polymer in different mixtures of solvents and justifies the proportionality found between KΘ deviations and the excess Gibbs free energy between both solvents of the solvent mixture.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1618-2650
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A multivariate study was applied to the investigation of the variables affecting the cadmium sensitivity in a graphite furnace, with and without platform atomization or matrix modifier. The results indicated that, depending on the atomization system used, the factors studied (drying, ashing, atomization, calibration curve) exert an influence on the analysis. The interactions between the factors were also analyzed.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 27 (1989), S. 1559-1597 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The Flory-Huggins theory as modified by Pouchlý has been applied to calculate preferential (λ) and total (Y) sorption coefficients for a ternary polymer system. The ternary interaction function (φ1φ2φ3GT(u1, φ3)) is described as the product of three independent binary functions. This expression allows prediction of λ and Y from binary interaction parameters χ130, χ230, g130, g230, and g12(φ10). Three ternary polymer systems are used to check the validity of the expression. Moreover for polymer systems in which the parameters g130 and/or g230 are unknown, a procedure to evaluate them has been developed and verified on systems for which sufficient experimental information is available.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A procedure has been developed, based on the Flory-Huggins theory as generalized by Pouchlý, which permits the calculation of preferential (λ) and total (Y) sorption coefficients from previous information on the binary interaction parameters, χ130, χ230, and g12(φ10) and on the mixture composition at which the sign of λ inverts. The expressions obtained were applied to 10 cosolvent polymer systems for which experimental values of λ and Y are known. Practically in all the studied systems, the theoretical predictions are in fair accordance with the experimental data.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Polymer International 36 (1995), S. 345-351 
    ISSN: 0959-8103
    Keywords: viscometry ; densimetry ; unperturbed dimensions ; preferential interactions ; poly(N-vinyl-2-pyrrolidone) ; CdCl2 ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The poly(N-vinyl-2-pyrrolidone)(PVP)(2)/water(1)/CdCl2(3) ternary system has been studied by viscometry, densimetry and atomic absorption spectrophotometry. In this system a preferential adsorption of Cd2+ at all solvent compositions studied and a conformational transition at 4mM of salt, the concentration at which a preferential adsorption minimum of Cd2+ in exhibited, are observed. The PVP/Cd2+ bound molar ratio is 0·23. CdCl2 behaves as a salting-in agent for the macromolecule. The binary solvent mixture is thermodynamically more favourable at salt concentrations greater than 10 mM of CdCl2.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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