1. Identification of karyopherin α1 and α7 interacting proteins in porcine tissue
- Author
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Ki-Eun Park, Xin Wang, S.L. Koser, H. Dorota Inerowicz, Ryan A. Cabot, and Yanfang Li
- Subjects
alpha Karyopherins ,Proteomics ,Cell Physiology ,Anatomy and Physiology ,Proteome ,Swine ,Science ,Importin ,Plasma protein binding ,Biology ,Biochemistry ,Peptide Mapping ,Chromatin remodeling ,Intracellular Receptors ,Animal Production ,Tandem Mass Spectrometry ,Animals ,Nuclear protein ,Karyopherin ,Fluorescent Dyes ,Animal Management ,chemistry.chemical_classification ,Multidisciplinary ,Spectrometric Identification of Proteins ,Proteins ,Alpha Karyopherins ,Agriculture ,Molecular biology ,Cell biology ,chemistry ,Medicine ,Nuclear transport ,Animal Genetics ,Sequence Analysis ,Nuclear localization sequence ,Chromatography, Liquid ,Protein Binding ,Research Article - Abstract
Specialized trafficking systems in eukaryotic cells serve a critical role in partitioning intracellular proteins between the nucleus and cytoplasm. Cytoplasmic proteins (including chromatin remodeling enzymes and transcription factors) must gain access to the nucleus to exert their functions to properly program fundamental cellular events ranging from cell cycle progression to gene transcription. Knowing that nuclear import mediated by members of the karyopherin α family of transport receptors plays a critical role in regulating development and differentiation, we wanted to determine the identity of proteins that are trafficked by this karyopherin α pathway. To this end, we performed a GST pull-down assay using porcine orthologs of karyopherin α1 (KPNA1) and karyopherin α7 (KPNA7) and prey protein derived from porcine fibroblast cells and used a liquid chromatography and tandem mass spectrometry (LC-MS/MS) approach to determine the identity of KPNA1 and KPNA7 interacting proteins. Our screen revealed that the proteins that interact with KPNA1 and KPNA7 are generally nuclear proteins that possess nuclear localization signals. We further validated two candidate proteins from this screen and showed that they are able to be imported into the nucleus in vivo and also interact with members of the karyopherin α family of proteins in vitro. Our results also reveal the utility of using a GST pull-down approach coupled with LC-MS/MS to screen for protein interaction partners in a non-traditional model system.
- Published
- 2012