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  • Chemistry  (3)
  • SPACECRAFT PROPULSION AND POWER
  • Surface physics, nanoscale physics, low-dimensional systems
  • 1975-1979  (2)
  • 1970-1974  (1)
  • 1
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Evidence is presented which shows that hemoglobin S in sickle cells has a tendency to aggregate even in the oxygenated state. The basis for that conclusion is derived from 13C-nmr rotating-frame spin-lattice relaxation studies in the presence of an off-resonance radiofrequency field in which the carbonyl resonances of hemoglobins in erythrocytes are examined. The experiments indicate that the rotational correlation time of hemoglobin S in oxygenated sickle cells at 38°C is 130 nsec compared to a value of 95 nsec for hemoglobin A in normal erythrocytes at the same temperature and the same mean cell hemoglobin content.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 13 (1974), S. 1317-1340 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The polymerization kinetics and optical rotatory properties of AnBm polypeptides have been studied, where A = D,L-Tyr, D,L-TyrZ, D,L-LysZ, L-AspOBzl, or L-Asp-ONBzl, and B = D,L-GluOR (R = Me or Bzl). In most cases where An and Bm prefer the same helix sense, the polymerization of A N-carboxyanhydride (initiated by Bm in dioxane) shows first order kinetics and produces a monotonic change in optical rotation, while if opposite helix senses are preferred, the kinetics are multiphasic and the change in rotation reverses direction after the addition of several residues. The rotation change in the latter case is interpreted to mean that the helix in the A block is initially induced to take the nonpreferred sense, as originally suggested by Doty and Lundberg from similar observations on (D-GluOBzl)n-(L-GluOBzl)m. It is found here that the CD spectra for the latter polymer show the sign changes required by this hypothesis. The optical rotation curves and CD spectra for (D,L-Tyr)n-(L-GluOBzl)20 suggest, by analogy, that (L-Tyr)n prefers the same helix sense as (L-GluOBzl)n. However, it is found that the opposite conclusion is equally consistent with the data if one considers the effects of possible changes in side-chain conformation on these data in accordance with the calculated CD spectra of Chen and Woody. The optical rotation curves for (D-GluOBzl)n-(L-GluOBzl)20, (D-Tyr)n-(L-GluOBzl)20, and (L-Tyr)n-(L-GluOBzl)20 are all found to be consistent with a two-state equilibrium model in which the A block initially takes on an induced conformation and has an increasing tendency to revert to its preferred conformation as n increases. It is concluded that in both D-Tyr and L-Tyr the side-chain and/or the backbone conformation is induced by the neighboring L-GluOBzl block, and the data do not distinguish which type of change is occurring. These results are discussed in connection with other observations bearing on the helix sense of (L-Tyr)n.
    Additional Material: 9 Ill.
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  • 3
    ISSN: 1052-9306
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: This paper describes the use of gas chromatography mass spectrometry for the confirmation of ephedrine in adulterated powdered ipecac and ipecac fluid extract. Deuteration studies of ephedrine hydrochloride and some related compounds were also performed in an attempt to postulate structures for some of the fragment ions appearing in the spectrum of ephedrine.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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