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  • 1
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 4 (1977), S. 159-171 
    ISSN: 1052-9306
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Chemical ionization mass spectrometry is used at low resolution to determine the sequences of permethylated acetyl peptides. The method has been tested with 45 peptides, between 2 and 5 residues long, including examples of all of the common amino acids except cysteine and N-terminal asparagine. The isobutane chemical ionization spectra contain three principal types of N-terminal sequence ion and one type of C-terminal sequence ion. The redundant information available from these four types of sequence ion increases the reliability of the sequence determination. In prospect, isobutane chemical ionization mass spectrometry seems to be a useful technique for peptide sequence determination, and may have advantages in some cases.
    Additional Material: 2 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 2 (1975), S. 164-167 
    ISSN: 1052-9306
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Chemical ionization mass spectra of eleven biomedically significant quaternary amimes are reported. The samples are converted to volatile compounds by known thermal decompositions. Chemical ionization of the compounds gives simple, easily identifiable spectra which are useful for the analysis of the original samples.
    Additional Material: 4 Tab.
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  • 3
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 2 (1975), S. 254-260 
    ISSN: 1052-9306
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The extent of C-methylation, an artifact of the permethylation procedure used to derivatize peptides for mass spectrometric sequencing, was investigated by mass spectrometry. Ten glycine-containing peptides were N-acetylated and then permethylated by the Hakomori method and analyzed by chemical ionization and, in some cases, by electron ionization mass spectrometry. A comparative study was made of the tripeptides Gly Pro Ala and Ala Pro Gly, derivatized by three permethylation procedures. The results show that while C-methylation occurs primarily at glycine, other amino acids (Gln, Glu, Met, Tyr) are also C-methylated, but to a lesser degree. The extent to which C-methylation occurs varies widely and depends on residue position and on the identity of neighboring residues. Such artifacts could lead to serious errors in peptide sequences determined by mass spectrometry, especially when mixtures of peptides are analyzed.
    Additional Material: 4 Tab.
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  • 4
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: The concept of surface-active comonomers of higher functionality is propsed as a means of increasing reliability of the bonding between preventive and restorative dental materials and tooth structures.
    Additional Material: 3 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 12 (1978), S. 505-515 
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: Initial rates of ion-exchange adsorption of nickelous or cupric ions with calcium ions on the surface of synthetic hydroxyapatite were studied in aqueous nitrate solutions. A kinetic interpretation has been proposed. The determination of the initial rates is important for a systematic investigation of adhesion of certain properly designe substances that may mediate a chemical bonding between dental resins and “moralanted” calcified tissues.
    Additional Material: 4 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Cellular Physiology 98 (1979), S. 81-94 
    ISSN: 0021-9541
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Balb/c3T3 cells in crowded cultures detach from the dish when deprived of serum, and the survivors incorporate 3H-thymidine at a reduced rate. The detachment becomes pronounced two hours after removal of serum, and reaches its maximum rate between two and four hours. Cells in sparse culture are not detached by serum removal, and their rate of 3H-thymidine incorporation is only slightly reduced. As the sparse cultures grow into more crowded cultures, and the serum is depleted, increasing numbers detach. The detached cells are incapable of reattaching when placed in a new dish with ample fresh serum. The cells are leaky to cellular constituents and appear to be dead. Detachment is a consequence rather than the cause of cell death, and can be produced by agents which inhibit cellular energy metabolism. The cells on the dish which survive serum deprivation are fully viable and grow rapidly when serum is added. When they become crowded they are as sensitive to serum deprivation as was the original population. They are therefore not selected for a low serum requirement but apparently survive because they spread into the space vacated by the detaching cells and then behave as sparse cultures in response to serum variations. Insoluble complexes of Ca2+ and pyrophosphate (Ca2+-PPi) show the same concentration dependence in promoting cell survival as in stimulating 3H-thymidine incorporation, showing that a single substance can be responsible for both activities. It is concluded that survival and growth are part of the coordinate response of 3T3 cells to single external effectors. The results are discussed in terms of a simple model in which the coordinate response is regulated by the availability of Mg2+ for transphosphorylation reactions within the cell, and the availability depends on the binding affinity of cellular membranes for Mg2+. The difference between survival and multiplication is postulated to be in the intensity and duration rather than the kind of stimulus.
    Additional Material: 10 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 91 (1979), S. 484-495 
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Organische Ionen zerfallen in den feldfreien Bereichen eines Massenspektrometers nach einer wohldefinierten Lebensdauer (t ≈ 10-5 s), die - verglichen mit der Zeitskala von Molekülschwingungen - sehr groß ist. Die im Übergangszustand einer Dissoziation vorhandene Überschußenergie („non fixed energy“) ist mit der von Reaktionen in Lösung vergleichbar. Allgemein gilt, daß nur die energetisch günstigsten Zerfallswege miteinander konkurrieren können. Die Analyse von Übergangssignalen der unimolekularen Zerfälle metastabiler Ionen liefert Informationen über die bei der Reaktion freigesetzte kinetische Energie („kinetic energy release“), T; bei Experimenten in Lösung sind diese äußerst wertvollen Daten aufgrund von Stößen nicht zugänglich. Die Chemie von Ionen kann bequem studiert werden, wenn man die Ionen in einem Massenspektrometer erzeugt und die Zerfälle metastabiler Ionen analysiert.
    Additional Material: 10 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 13 (1978), S. 721-728 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The unimolecular decompositions of two isomers of [C3H8N]+, \documentclass{article}\pagestyle{empty}\begin{document}$ {\rm CH}_{\rm 3} {\rm CH}_{\rm 2} {\rm CH} = \mathop {\rm N}\limits^ + {\rm H}_2 $\end{document} and \documentclass{article}\pagestyle{empty}\begin{document}$ {\rm CH}_{\rm 3} {\rm CH}_{\rm 2} \mathop {\rm N}\limits^ + {\rm H = CH}_{\rm 2} $\end{document}, are discussed in terms of the potential energy profile over which reaction may be considered to occur. The energy needed to promote slow (metastable) dissociations of either ion is found to be less than that required to cause isomerization to the other structure. This finding is supported by the observation of different decomposition pathways, different metastable peak shapes for C2H4 loss, the results of 2H labelling studies, and energy measurements on the two ions. The corresponding potential energy profile for decomposition of the oxygen analogues, \documentclass{article}\pagestyle{empty}\begin{document}${\rm CH}_{\rm 3} {\rm CH}_{\rm 2} {\rm CH =\!= }\mathop {\rm O}\limits^ + {\rm H} $\end{document} and \documentclass{article}\pagestyle{empty}\begin{document}$ {\rm CH}_{\rm 3} {\rm CH}_{\rm 2} \mathop {\rm O}\limits^ + {\rm = CH}_{\rm 2} $\end{document}, is compared and contrasted with that proposed for the [C3H8N]+ isomers. This analysis indicates that for the oxygen analogues, the energy needed to decompose either ion is very similar to that required to cause isomerization to the other structure. Consequently, dissociation of either ion is finely balanced with rearrangement to the other and similar reactions are observed. Detailed mechanisms are proposed for loss of H2O and C2H4 from each ion and it is shown that these mechanisms are consistent with 2H and 13C labelling studies, the kinetic energy release associated with each decomposition channel, the relative competition between H2O and C2H4 loss and energy measurements.
    Additional Material: 2 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 11 (1976), S. 223-230 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: It is shown that the ‘metastable’ mass spectra of a series of monosubstituted benzenes are consistent with reaction over the lowest available energy surfaces. The non-occurrence of some qualitatively possible decomposition pathways may therefore be used to place lower limits on the heats of formation of gaseous cations. Conversely, where characterized reactions are preempted by new reactions upon introduction of additional substituents, upper limits may be placed upon the heats of formation of the ionic products of the new reactions. The concepts are employed to deduce that C3H6 elimination from n-butylbenzence subsequent to ionization leads to ionized toluene rather than ionized methyleneclohexadience.
    Additional Material: 3 Tab.
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  • 10
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 12 (1977), S. 453-460 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The concept that the slow, unimolecular reactions of the homologous series of radical cations are largely determined by the relative energetics of the possible product combinations is discussed. The concept is shown to provide a reasonably consistent rationalization of the known metastable dissociations of and correctly predicts the reactions undergone by . The concept may be useful in discussing the unimolecular chemistry of isomers.
    Additional Material: 4 Ill.
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