Literature DB >> 12973721

Analysis of human serum proteins by liquid phase isoelectric focusing and matrix-assisted laser desorption/ionization-mass spectrometry.

Michael Z Wang1, Brandon Howard, Michael J Campa, Edward F Patz, Michael C Fitzgerald.   

Abstract

Direct matrix-assisted laser desorption/ionization-time of flight mass spectrometry (MALDI-TOF MS) analysis of human serum yielded ion signals from only a fraction of the total number of peptides and proteins expected to be in the sample. We increased the number of peptide and protein ion signals observed in the MALDI-TOF mass spectra analysis of human serum by using a prefractionation protocol based on liquid phase isoelectric focusing electrophoresis. This pre-fractionation technique facilitated the MALDI-TOF MS detection of as many as 262 different peptide and protein ion signals from human serum. The results obtained from three replicate fractionation experiments on the same serum sample indicated that 148 different peptide and protein ion signals were reproducibly detected using our isoelectric focusing and MALDI-TOF MS protocol.

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Year:  2003        PMID: 12973721     DOI: 10.1002/pmic.200300513

Source DB:  PubMed          Journal:  Proteomics        ISSN: 1615-9853            Impact factor:   3.984


  2 in total

1.  Parametric power spectral density analysis of noise from instrumentation in MALDI TOF mass spectrometry.

Authors:  Hyunjin Shin; Miray Mutlu; John M Koomen; Mia K Markey
Journal:  Cancer Inform       Date:  2007-09-17

2.  Characterising phase variations in MALDI-TOF data and correcting them by peak alignment.

Authors:  Simon M Lin; Richard P Haney; Michael J Campa; Michael C Fitzgerald; Edward F Patz
Journal:  Cancer Inform       Date:  2005
  2 in total

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