Literature DB >> 12845586

Automated protein identification using atmospheric-pressure matrix-assisted laser desorption/ionization.

John T Mehl1, John J Cummings, Ellen Rohde, Nathan N Yates.   

Abstract

Atmospheric-pressure matrix-assisted laser desorption/ionization (AP-MALDI) ion trap mass spectrometry (ITMS) has been evaluated for automated protein identification. By using signal averaging and long ion-injection times, protein identification limits in the 50-fmol range are achieved for standard protein digests. Data acquisition requires 7.5 min or less per sample and the MS/MS spectra files are automatically processed using the SEQUEST database searching algorithm. AP-MALDI-ITMS was compared with the widely used methods of microLC/MS/MS (ion trap) and automated MALDI-TOF peptide mass mapping. Sample throughput is 10-fold greater using AP-MALDI compared with microcapillary liquid chromatography/tandem mass spectrometry (microLC/MS/MS). The protein sequence coverage obtained from AP-MALDI-MS/MS spectra matched by SEQUEST is lower compared with microLC/MS/MS and MALDI-TOF mass mapping. However, by using the AP-MALDI full-scan peptide mass fingerprint spectrum, sequence coverage is increased. AP-MALDI-ITMS was applied for the analysis of Coomassie blue stained gels and was found to be a useful platform for rapid protein identification. Copyright 2003 John Wiley & Sons, Ltd.

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Year:  2003        PMID: 12845586     DOI: 10.1002/rcm.1092

Source DB:  PubMed          Journal:  Rapid Commun Mass Spectrom        ISSN: 0951-4198            Impact factor:   2.419


  1 in total

1.  On-chip solid-phase extraction pre-concentration/focusing substrates coupled to atmospheric pressure matrix-assisted laser desorption/ionization ion trap mass spectrometry for high sensitivity biomolecule analysis.

Authors:  Arti Navare; Marcela Nouzova; Fernando G Noriega; Salvador Hernández-Martínez; Christoph Menzel; Facundo M Fernández
Journal:  Rapid Commun Mass Spectrom       Date:  2009-02       Impact factor: 2.419

  1 in total

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