NP-40 reduces contamination by endogenous biotinylated carboxylases during purification of biotin tagged nuclear proteins

•Comparing nuclear extract methods to reduce biotinylated cytoplasmic carboxylases.•NP-40 significantly reduces nuclear contamination by carboxylases.•Mass spec shows reduced carboxylase background binding to streptavidin beads.•Method is widely applicable for nuclear protein purification by biotin...

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Veröffentlicht in:Protein expression and purification 2013-05, Vol.89 (1), p.80-83
Hauptverfasser: Papageorgiou, Dimitris N., Demmers, Jeroen, Strouboulis, John
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Sprache:eng
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Zusammenfassung:•Comparing nuclear extract methods to reduce biotinylated cytoplasmic carboxylases.•NP-40 significantly reduces nuclear contamination by carboxylases.•Mass spec shows reduced carboxylase background binding to streptavidin beads.•Method is widely applicable for nuclear protein purification by biotin tagging. We describe here a simple procedure for greatly reducing contamination of nuclear extracts by naturally biotinylated cytoplasmic carboxylases, which represent a major source of non-specific background when employing BirA-mediated biotinylation tagging for the purification and characterization of nuclear protein complexes by mass spectrometry. We show that the use of 0.5% of the non-ionic detergent Nonidet-40 (NP-40) during cell lysis and nuclei isolation is sufficient to practically eliminate contamination of nuclear extracts by carboxylases and to greatly reduce background signals in downstream mass spectrometric analyses.
ISSN:1046-5928
1096-0279
DOI:10.1016/j.pep.2013.02.015