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Methods. 2011 Aug;54(4):379-86. doi: 10.1016/j.ymeth.2011.03.008. Epub 2011 Apr 1.

A solid phase extraction-based platform for rapid phosphoproteomic analysis.

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1
Department of Cell Biology, Harvard Medical School, Boston, MA 02115, USA. noah_dephoure@hms.harvard.edu

Abstract

Protein phosphorylation is among the most common and intensely studied post-translational protein modification. It plays crucial roles in virtually all cellular processes and has been implicated in numerous human diseases, including cancer. Traditional biochemical and genetic methods for identifying and monitoring sites of phosphorylation are laborious and slow and in recent years have largely been replaced by mass spectrometric analysis. Improved methods for phosphopeptide enrichment coupled with faster and more sensitive mass spectrometers have led to an explosion in the size of phosphoproteomic datasets. However, wider application of these methods is limited by equipment costs and the resultant high demand for instrument time as well as by a technology gap between biologists and mass spectrometrists. Here we describe a modified two-step enrichment strategy that employs lysC digestion and step elution from self-packed strong cation exchange (SCX) solid phase extraction (SPE) columns followed by immobilized metal ion affinity chromatography (IMAC) and LC-MS/MS analysis using a hybrid LTQ Orbitrap Velos mass spectrometer. The SCX procedure does not require an HPLC system, demands little expertise, and because multiple samples can be processed in parallel, can provide a large savings of time and labor. We demonstrate this method in conjunction with stable isotope labeling to quantitate peptides harboring >8000 unique phosphorylation sites in yeast in 12h of instrument analysis time and examine the impact of enzyme choice and instrument platform.

PMID:
21440633
PMCID:
PMC3156280
DOI:
10.1016/j.ymeth.2011.03.008
[Indexed for MEDLINE]
Free PMC Article
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