Abstract | BACKGROUND: RESULTS: The experimental design included immunoaffinity depletion of 12 most abundant proteins from plasma samples with the ProteomeLab IgY-12 LC10 column kit as first dimension separation, also referred to as immuno-partitioning. Second and third dimension separations of the enriched proteome were performed on the PF 2D platform utilizing 2D isoelectric focusing and RP-HPLC with the resulting fractions collected for analysis. 1D gel electrophoresis was added as a fourth dimension when sufficient protein was available. Protein identification from collected fractions was performed using nano-LC-MS/MS approach. Analysis of differences in the resulting two-dimensional maps of fractions obtained from the PF 2D and the ability to identify proteins from these fractions allowed sensitivity threshold measurements. Masked proteins in the PF 2D fractions are discussed. CONCLUSION: We offer some insight into the strengths and limitations of this emerging proteomic platform.
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Authors | Joshua D Schlautman, Wojciech Rozek, Robert Stetler, R Lee Mosley, Howard E Gendelman, Pawel Ciborowski |
Journal | Proteome science
(Proteome Sci)
Vol. 6
Pg. 26
(Sep 12 2008)
ISSN: 1477-5956 [Electronic] England |
PMID | 18789151
(Publication Type: Journal Article)
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