کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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1195835 | 964416 | 2008 | 8 صفحه PDF | دانلود رایگان |
Liquid chromatography/quadrupole time of flight mass spectrometry (LC/QTOF MS) utilizing electrospray ionization was employed to monitor protein expression in Escherichia coli and Shigella organisms. Comparison with MALDI/TOF-MS revealed more proteins, particularly above 15 kDa. A combination of automated charge state deconvolution, spectral mirroring, and spectral subtraction was used to reveal subtle differences in the LC/MS data. Reproducible intact protein biomarker candidates were discovered based on their unique mass, retention time, and relative intensity. These marker candidates were implemented to differentiate closely related strain types, (e.g., two distinct isolates of E. coli O157:H7) and to correctly identify unknown pathogens. This LC/MS approach is less labor-intensive than pulsed-field gel electrophoresis, affords greater specificity than real-time PCR, and requires no primers or antibodies. Additionally, this approach would be beneficial during outbreaks of foodborne disease or bioterrorism investigations by complementing methods typically used in diagnostic microbiology laboratories.
Graphical AbstractLC/QTOF MS combined with automated charge state deconvolution, spectral mirroring, and spectral subtraction were utilized to distinguish E. coli O157:H7 strains having identical clinical manifestation.Figure optionsDownload high-quality image (219 K)Download as PowerPoint slide
Journal: Journal of the American Society for Mass Spectrometry - Volume 19, Issue 11, November 2008, Pages 1621–1628