Literature DB >> 21819303

Challenges in plasma membrane phosphoproteomics.

Benjamin C Orsburn1, Luke H Stockwin, Dianne L Newton.   

Abstract

The response to extracellular stimuli often alters the phosphorylation state of plasma membrane- associated proteins. In this regard, generation of a comprehensive membrane phosphoproteome can significantly enhance signal transduction and drug mechanism studies. However, analysis of this subproteome is regarded as technically challenging, given the low abundance and insolubility of integral membrane proteins, combined with difficulties in isolating, ionizing and fragmenting phosphopeptides. In this article, we highlight recent advances in membrane and phosphoprotein enrichment techniques resulting in improved identification of these elusive peptides. We also describe the use of alternative fragmentation techniques, and assess their current and future value to the field of membrane phosphoproteomics.

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Year:  2011        PMID: 21819303      PMCID: PMC3164310          DOI: 10.1586/epr.11.40

Source DB:  PubMed          Journal:  Expert Rev Proteomics        ISSN: 1478-9450            Impact factor:   3.940


  90 in total

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4.  SIMAC (sequential elution from IMAC), a phosphoproteomics strategy for the rapid separation of monophosphorylated from multiply phosphorylated peptides.

Authors:  Tine E Thingholm; Ole N Jensen; Phillip J Robinson; Martin R Larsen
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Review 5.  Analytical strategies for phosphoproteomics.

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Journal:  Proteomics       Date:  2009-03       Impact factor: 3.984

Review 6.  Hydrophilic interaction chromatography for fractionation and enrichment of the phosphoproteome.

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7.  Lys-N and trypsin cover complementary parts of the phosphoproteome in a refined SCX-based approach.

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