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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Rapid Communications in Mass Spectrometry 4 (1990), S. 297-299 
    ISSN: 0951-4198
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: In standard pulsed ion cyclotron resonance mass spectrometry (ICRMS) mass spectra are generated by converting the time domain signal to the frequency or mass domain by fast Fourier transform (FFT). The FFT requires long acquisition times to acquire high resolution mass spectra. In ICRMS, long acquisition times introduce distortions in the peak intensities of the transformed spectrum that lead to errors in ion abundance. We report here the use of linear prediction methods on data sets collected during much shorter acquisition times to determine actual ion abundances more accurately.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 17 (1988), S. 411-414 
    ISSN: 1052-9306
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 19 (1990), S. 286-294 
    ISSN: 1052-9306
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The electrospray ionization (ESI) and plasma desorption (PD) mass spectra of over 20 peptides and proteins, with molecular weights (Mr) ranging between 1182 and 143000, have been directly compared. Both techniques produced molecular ions for the majority of materials studied; however, neither approach proved to be universally applicable. PD failed for a number of proteins that were successfully analyzed by ESI, including some of very high Mr. On the other hand, ESI failed for proteins that apparently could not acquire a sufficient number of positive charges to allow transmission through the quadrupole mass filter. A non-covalently bound adduct, ribonuclease S, did not survive either method intact and a simple glycoprotein, ribonuclease B, did not yield the expected molecular ion with either approach. The mass measurement accuracy of quadrupole ESI is five to tenfold better than obtained with a commercial time-of-flight PD mass spectrometer. Furthermore, ESI's superior mass resolution (with quadrupole mass spectrometers) will prove to be particularly helpful for the characterization of mixtures of closely related materials. Sensitivity was only compared qualitatively but is highly compound dependent with both techniques. In favorable cases, ESI spectra can be obtained on low femtomolar quantities of proteins while PD typically requires several hundred femtomoles to high picomoles, depending on a number of factors including Mr.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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