Literature DB >> 19251440

Reactive landing of gas-phase ions as a tool for the fabrication of metal oxide surfaces for in situ phosphopeptide enrichment.

Grady R Blacken1, Michael Volný, Matthew Diener, Karl E Jackson, Pratistha Ranjitkar, Dustin J Maly, Frantisek Turecek.   

Abstract

Zirconium, titanium, and hafnium oxide-coated stainless steel surfaces are fabricated by reactive landing of gas-phase ions produced by electrospray ionization of group IVB metal alkoxides. The surfaces are used for in situ enrichment of phosphopeptides before analysis by matrix-assisted laser desorption ionization (MALDI) mass spectrometry. To evaluate this method we characterized ZrO(2) (zirconia) surfaces by (1) comparison with the other group IVB metal oxides of TiO(2) (titania) and HfO(2) (hafnia), (2) morphological characterization by SEM image analysis, and (3) dependence of phosphopeptide enrichment on the metal oxide layer thickness. Furthermore, we evaluated the necessity of the reactive landing process for the construction of useful metal oxide surfaces by preparing surfaces by electrospray deposition of Zr, Ti, and Hf alkoxides directly onto polished metal surfaces at atmospheric pressure. Although all three metal oxide surfaces evaluated were capable of phosphopeptide enrichment from complex peptide mixtures, zirconia performed better than hafnia or titania as a result of morphological characteristics illustrated by the SEM analysis. Metal oxide coatings that were fabricated by atmospheric pressure deposition were still capable of in situ phosphopeptide enrichment, although with inferior efficiency and surface durability. We show that zirconia surfaces prepared by reactive landing of gas-phase ions can be a useful tool for high throughput screening of novel phosphorylation sites and quantitation of phosphorylation kinetics.

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Year:  2009        PMID: 19251440     DOI: 10.1016/j.jasms.2009.01.006

Source DB:  PubMed          Journal:  J Am Soc Mass Spectrom        ISSN: 1044-0305            Impact factor:   3.109


  36 in total

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Review 4.  Characterizing phosphoproteins and phosphoproteomes using mass spectrometry.

Authors:  Michael B Goshe
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Authors:  Shabaz Mohammed; Karsten Kraiczek; Martijn W H Pinkse; Simone Lemeer; Joris J Benschop; Albert J R Heck
Journal:  J Proteome Res       Date:  2008-02-29       Impact factor: 4.466

6.  High yield bacterial expression of active c-Abl and c-Src tyrosine kinases.

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7.  Selective isolation at the femtomole level of phosphopeptides from proteolytic digests using 2D-NanoLC-ESI-MS/MS and titanium oxide precolumns.

Authors:  Martijn W H Pinkse; Pauliina M Uitto; Martijn J Hilhorst; Bert Ooms; Albert J R Heck
Journal:  Anal Chem       Date:  2004-07-15       Impact factor: 6.986

8.  Autophosphorylation of Src and Yes blocks their inactivation by Csk phosphorylation.

Authors:  G Sun; A K Sharma; R J Budde
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9.  Selective zirconium dioxide-based enrichment of phosphorylated peptides for mass spectrometric analysis.

Authors:  Hye Kyong Kweon; Kristina Håkansson
Journal:  Anal Chem       Date:  2006-03-15       Impact factor: 6.986

10.  Evaluation of the impact of some experimental procedures on different phosphopeptide enrichment techniques.

Authors:  Søren S Jensen; Martin R Larsen
Journal:  Rapid Commun Mass Spectrom       Date:  2007       Impact factor: 2.419

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  2 in total

Review 1.  Recent advances in enrichment and separation strategies for mass spectrometry-based phosphoproteomics.

Authors:  Chenxi Yang; Xuefei Zhong; Lingjun Li
Journal:  Electrophoresis       Date:  2014-06-16       Impact factor: 3.535

2.  In situ SIMS and IR spectroscopy of well-defined surfaces prepared by soft landing of mass-selected ions.

Authors:  Grant E Johnson; K Don Dasitha Gunaratne; Julia Laskin
Journal:  J Vis Exp       Date:  2014-06-16       Impact factor: 1.355

  2 in total

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