| Literature DB >> 21871587 |
Mario Pink1, Nisha Verma, Fabio Polato, Günther K Bonn, Hideo A Baba, Albert W Rettenmeier, Simone Schmitz-Spanke.
Abstract
Posttranslational modification (PTM) of proteins, particularly phosphorylation, is a key element in the regulation of cell functions. In many signal transduction processes, PTM is a pivotal step. Various analytical methods have been proposed for the identification of phosphoproteins; however, most of these methods require sophisticated equipment. Here we present an easily applicable method of phosphoprotein enrichment. This method is based on single-step precipitation by lanthanum chloride and allows subsequent protein identification by matrix-assisted laser desorption/ionization-mass spectrometry (MALDI-TOF-MS). The method proved its suitability for the isolation of phosphoproteins from frozen tissue and cultured cells samples after cell lysis in various buffer systems (urea/thiourea and EGTA/EDTA). The tests revealed that the isolation of phosphoproteins can be achieved with high efficiency even from complex protein mixtures. Our results indicate that lanthanum-based enrichment of phosphoproteins can be a useful tool in phosphoproteomic studies.Entities:
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Year: 2011 PMID: 21871587 DOI: 10.1016/j.jprot.2011.08.001
Source DB: PubMed Journal: J Proteomics ISSN: 1874-3919 Impact factor: 4.044