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...
Gespeichert in:
Veröffentlicht in: | Protein expression and purification 2013-05, Vol.89 (1), p.80-83 |
---|---|
Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
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 |