Literature DB >> 17584176

Enrichment of multiphosphorylated peptides by immobilized metal affinity chromatography using Ga(III)- and Fe(III)-complexes.

Corinna Sykora1, Ralf Hoffmann, Peter Hoffmann.   

Abstract

The detection and identification of O-phosphorylation sites in proteins with mass spectrometry remains a challenge. A common approach to analyse these modifications is to enrich phosphopeptides by immobilized metal affinity chromatography (IMAC) prior to mass spectrometric analysis. In this study two commercially available IMAC kits based on Fe(III)-ions immobilized on magnetic beads and Ga(III)-ions immobilized on a chelate-resin, have been investigated and the binding efficiency of peptide mixtures containing non-phosphorylated, singly, doubly and triply phosphorylated peptides have been tested.

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Year:  2007        PMID: 17584176     DOI: 10.2174/092986607780782849

Source DB:  PubMed          Journal:  Protein Pept Lett        ISSN: 0929-8665            Impact factor:   1.890


  3 in total

1.  Scalable, Non-denaturing Purification of Phosphoproteins Using Ga3+-IMAC: N2A and M1M2 Titin Components as Study case.

Authors:  Michael Adams; Jennifer R Fleming; Eva Riehle; Tiankun Zhou; Thomas Zacharchenko; Marija Markovic; Olga Mayans
Journal:  Protein J       Date:  2019-04       Impact factor: 2.371

Review 2.  Application of proteomics to neutrophil biology.

Authors:  Gregory C Luerman; Silvia M Uriarte; Madhavi J Rane; Kenneth R McLeish
Journal:  J Proteomics       Date:  2009-07-04       Impact factor: 4.044

3.  A phosphorylation tag for uranyl mediated protein purification and photo assisted tag removal.

Authors:  Qiang Zhang; Thomas J D Jørgensen; Peter E Nielsen; Niels Erik Møllegaard
Journal:  PLoS One       Date:  2014-03-05       Impact factor: 3.240

  3 in total

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