Analysis of protein phosphorylation by monolithic extraction columns based on poly(divinylbenzene) containing embedded titanium dioxide and zirconium dioxide nano‐powders

The potential of an organic monolith with incorporated titanium dioxide (TiO2) and zirconium dioxide (ZrO2) nanoparticles was evaluated for the selective enrichment of phosphorylated peptides from tryptic digests. A pipette tip was fitted with a monolith based on divinylbenzene (DVB) of highly porous structure, which allows sample to pass through the monolithic bed. The enrichment of phosphopeptides was enhanced by increasing the pipetting cycles during the sample preparation and a higher recovery could be achieved with adequate buffer systems. A complete automated process was developed for enrichment of phosphopeptides leading to high reproducibility and resulting in a robust method designed to minimize analytical variance while providing high sensitivity at high sample throughput. The effect of particle size on the selectivity of phosphopeptides was investigated by comparative studies with nano‐ and microscale TiO2 and ZrO2 powders. Eleven phosphopeptides from α‐casein digest could be recovered by an optimized mixture of microscale TiO2/ZrO2 particles, whereas nine additional phosphopeptides could be retained by the same mixture of nano‐structured material. When compared to conventional immobilized metal‐ion affinity chromatography and commercial phosphorylation‐enrichment kits, higher selectivity was observed in case of self fabricated tips. About 20 phosphopeptides could be retained from α‐casein and five from β‐casein digests by using TiO2 and ZrO2 based extraction tips. Further selectivity for phosphopeptides was demonstrated by enriching a digest of in vitro phosphorylated extracellular signal regulated kinase 1 (ERK1). Two phosphorylated peptides of ERK1 could be identified by MALDI‐MS/MS measurements and a following MASCOT database search.

[1]  C. Huck,et al.  Development and application of C60-fullerene bound silica for solid-phase extraction of biomolecules. , 2007, Analytical chemistry.

[2]  Xiaogang Jiang,et al.  Highly specific enrichment of phosphopeptides by zirconium dioxide nanoparticles for phosphoproteome analysis , 2007, Electrophoresis.

[3]  J. Yates,et al.  Optimizing TiO2-based phosphopeptide enrichment for automated multidimensional liquid chromatography coupled to tandem mass spectrometry. , 2007, Analytical chemistry.

[4]  Hye Kyong Kweon,et al.  Selective zirconium dioxide-based enrichment of phosphorylated peptides for mass spectrometric analysis. , 2006, Analytical chemistry.

[5]  W. Weckwerth,et al.  Enrichment of phosphorylated proteins and peptides from complex mixtures using metal oxide/hydroxide affinity chromatography (MOAC) , 2005, Proteomics.

[6]  C. Huck,et al.  Poly(glycidyl methacrylate/divinylbenzene)-IDA-FeIII in phosphoproteomics. , 2005, Journal of proteome research.

[7]  P. Roepstorff,et al.  Highly Selective Enrichment of Phosphorylated Peptides from Peptide Mixtures Using Titanium Dioxide Microcolumns* , 2005, Molecular & Cellular Proteomics.

[8]  G. Bonn,et al.  Characterisation and evaluation of metal-loaded iminodiacetic acid-silica of different porosity for the selective enrichment of phosphopeptides. , 2005, Journal of chromatography. A.

[9]  Isabel Feuerstein,et al.  Phosphoproteomic analysis using immobilized metal ion affinity chromatography on the basis of cellulose powder , 2005, Proteomics.

[10]  A. Heck,et al.  Selective isolation at the femtomole level of phosphopeptides from proteolytic digests using 2D-NanoLC-ESI-MS/MS and titanium oxide precolumns. , 2004, Analytical chemistry.

[11]  A. Stensballe,et al.  Large-scale Analysis of in Vivo Phosphorylated Membrane Proteins by Immobilized Metal Ion Affinity Chromatography and Mass Spectrometry* , 2003, Molecular & Cellular Proteomics.

[12]  Natalie G. Ahn,et al.  Identification of Novel Phosphorylation Sites on Xenopus laevis Aurora A and Analysis of Phosphopeptide Enrichment by Immobilized Metal-affinity Chromatography * , 2003, Molecular & Cellular Proteomics.

[13]  J. Shabanowitz,et al.  Phosphoproteome Analysis of Capacitated Human Sperm , 2003, The Journal of Biological Chemistry.

[14]  Hanno Steen,et al.  A new derivatization strategy for the analysis of phosphopeptides by precursor ion scanning in positive ion mode , 2002, Journal of the American Society for Mass Spectrometry.

[15]  Hanno Steen,et al.  Analysis of protein phosphorylation using mass spectrometry: deciphering the phosphoproteome. , 2002, Trends in biotechnology.

[16]  C. Borchers,et al.  Direct MALDI-MS/MS of phosphopeptides affinity-bound to immobilized metal ion affinity chromatography beads. , 2002, Analytical chemistry.

[17]  P. Cohen,et al.  The origins of protein phosphorylation , 2002, Nature Cell Biology.

[18]  R. Majors New designs and formats in solid-phase extraction sample preparation , 2001 .

[19]  W. Kolch Meaningful relationships: the regulation of the Ras/Raf/MEK/ERK pathway by protein interactions. , 2000, The Biochemical journal.

[20]  O. Okaya,et al.  Macroporous copolymer networks , 2000 .

[21]  A. J. McQuillan,et al.  Phosphate Adsorption onto TiO2 from Aqueous Solutions: An in Situ Internal Reflection Infrared Spectroscopic Study , 1999 .

[22]  V. Lopata,et al.  Porosity Measurements of Advanced Composites using Mercury Intrusion Porosimetry – A new quality tool , 1999 .

[23]  J. Porath,et al.  Immobilized-metal affinity chromatography of serum proteins on gel-immobilized group III A metal ions. , 1983, Archives of biochemistry and biophysics.

[24]  J. Porath,et al.  Metal chelate affinity chromatography, a new approach to protein fractionation , 1975, Nature.

[25]  Ralph G. Pearson,et al.  HARD AND SOFT ACIDS AND BASES , 1963 .

[26]  L. C. Drake,et al.  Macropore-Size Distributions in Some Typical Porous Substances , 1945 .