Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/49574
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Type: Journal article
Title: Enrichment of multiphosphorylated peptides by immobilized metal affinity chromatography using Ga(III)- and Fe(III)-complexes
Author: Sykora, C.
Hoffmann, R.
Hoffmann, P.
Citation: Protein and Peptide Letters: international journal for rapid publication of short papers in protein and peptide science, 2007; 14(5):489-496
Publisher: Bentham Science Publ Ltd
Issue Date: 2007
ISSN: 0929-8665
1875-5305
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.
Keywords: Humans
Gallium
Ferric Compounds
Trypsin
Phosphopeptides
Ovalbumin
tau Proteins
Caseins
Reagent Kits, Diagnostic
Chromatography, Affinity
Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
DOI: 10.2174/092986607780782849
Description (link): http://www.bentham.org/ppl/contabs/ppl14-5.htm#14
Published version: http://dx.doi.org/10.2174/092986607780782849
Appears in Collections:Aurora harvest 5
Molecular and Biomedical Science publications

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