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J Proteomics. 2010 Mar 10;73(5):829-44. doi: 10.1016/j.jprot.2009.12.003. Epub 2009 Dec 22.

2D-electrophoresis and the urine proteome map: where do we stand?

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1
Laboratory on Pathophysiology of Uremia, G Gaslini Children Hospital, Genoa, Italy.

Abstract

The discovery of urinary biomarkers is a main topic in clinical medicine. The development of proteomics has rapidly changed the knowledge on urine protein composition and probably will modify it again. Two-dimensional electrophoresis (2D-PAGE) coupled with mass spectrometry has represented for years the technique of choice for the analysis of urine proteins and it is time to draw some conclusions. This review will focus on major methodological aspects related to urine sample collection, storage and analysis by 2D-PAGE and attempt to define an advanced normal urine protein map. Overall, 1118 spots were reproducibly found in normal urine samples but only 275 were characterized as isoforms of 82 proteins. One-hundred height spots belonging to 30 proteins were also detected in plasma and corresponded to typical plasma components. The identity of most of the proteins found in normal urine by 2D-PAGE remains to be determined, the majority being low-molecular weight proteins (<30 kDa). Equalization procedures would also enhance sensitivity of the analysis and allow low abundance proteins to be characterized. Therefore, we are still on the way to define the normal urine composition. Technology advancements in concentrating procedure will improve sensitivity and give the possibility to purify proteins for mass spectrometry.

PMID:
20004755
DOI:
10.1016/j.jprot.2009.12.003
[Indexed for MEDLINE]
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