» Articles » PMID: 36952199

Affinity Purification of Soluble and Membrane-Bound Protein Complexes by a FlpIn Strategy

Overview
Specialty Molecular Biology
Date 2023 Mar 23
PMID 36952199
Authors
Affiliations
Soon will be listed here.
Abstract

For a long time, the isolation of native protein complexes from human cells was accomplished by immunoprecipitation experiments. However, success depends on the quality of the antibodies and the method consumes valuable antibodies, which can hinder subsequent analysis of the isolated complexes. Here, we demonstrate an alternative approach based on affinity purification. It utilizes human Flp-In cells, which genomically express a Protein A-tagged version of the human peroxisomal import receptor PEX5L. Native soluble and membrane-bound complexes containing PEX5L can thereby be isolated via a well-known affinity-based strategy.

References
1.
Nilsson J, Stahl S, Lundeberg J, Uhlen M, Nygren P . Affinity fusion strategies for detection, purification, and immobilization of recombinant proteins. Protein Expr Purif. 1997; 11(1):1-16. DOI: 10.1006/prep.1997.0767. View

2.
Agne B, Meindl N, Niederhoff K, Einwachter H, Rehling P, Sickmann A . Pex8p: an intraperoxisomal organizer of the peroxisomal import machinery. Mol Cell. 2003; 11(3):635-46. DOI: 10.1016/s1097-2765(03)00062-5. View

3.
Grunau S, Schliebs W, Linnepe R, Neufeld C, Cizmowski C, Reinartz B . Peroxisomal targeting of PTS2 pre-import complexes in the yeast Saccharomyces cerevisiae. Traffic. 2009; 10(4):451-60. DOI: 10.1111/j.1600-0854.2008.00876.x. View

4.
Oeljeklaus S, Reinartz B, Wolf J, Wiese S, Tonillo J, Podwojski K . Identification of core components and transient interactors of the peroxisomal importomer by dual-track stable isotope labeling with amino acids in cell culture analysis. J Proteome Res. 2012; 11(4):2567-80. DOI: 10.1021/pr3000333. View

5.
Meinecke M, Cizmowski C, Schliebs W, Kruger V, Beck S, Wagner R . The peroxisomal importomer constitutes a large and highly dynamic pore. Nat Cell Biol. 2010; 12(3):273-7. DOI: 10.1038/ncb2027. View