%0 Journal Article %1 oeljeklausIdentificationCoreComponents2012a %A Oeljeklaus, Silke %A Reinartz, Benedikt S. %A Wolf, Janina %A Wiese, Sebastian %A Tonillo, Jason %A Podwojski, Katharina %A Kuhlmann, Katja %A Stephan, Christian %A Meyer, Helmut E. %A Schliebs, Wolfgang %A Brocard, Cécile %A Erdmann, Ralf %A Warscheid, Bettina %C United States %D 2012 %J Journal of proteome research %K Acids/chemistry/metabolism,Chromatography Amino Design,Saccharomyces Fragments/analysis/chemistry/metabolism,Peroxisomes/*chemistry/metabolism,Protein High Interaction Labeling/*methods,Peptide Liquid,Isotope Maps,Proteomics/*methods,Research Mass Pressure Proteins/analysis/chemistry/metabolism,Saccharomyces Spectrometry,to_read cerevisiae cerevisiae/metabolism,Tandem %N 4 %P 2567--2580 %R 10.1021/pr3000333 %T Identification of Core Components and Transient Interactors of the Peroxisomal Importomer by Dual-Track Stable Isotope Labeling with Amino Acids in Cell Culture Analysis. %V 11 %X The importomer complex plays an essential role in the biogenesis of peroxisomes by mediating the translocation of matrix proteins across the organellar membrane. A central part of this highly dynamic import machinery is the docking complex consisting of Pex14p, Pex13p, and Pex17p that is linked to the RING finger complex (Pex2p, Pex10p, Pex12p) via Pex8p. To gain detailed knowledge on the molecular players governing peroxisomal matrix protein import and, thus, the integrity and functionality of peroxisomes, we aimed at a most comprehensive investigation of stable and transient interaction partners of Pex14p, the central component of the importomer. To this end, we performed a thorough quantitative proteomics study based on epitope tagging of Pex14p combined with dual-track stable isotope labeling with amino acids in cell culture-mass spectrometry (SILAC-MS) analysis of affinity-purified Pex14p complexes and statistics. The results led to the establishment of the so far most extensive Pex14p interactome, comprising 9 core and further 12 transient components. We confirmed virtually all known Pex14p interaction partners including the core constituents of the importomer as well as Pex5p, Pex11p, Pex15p, and Dyn2p. More importantly, we identified new transient interaction partners (Pex25p, Hrr25p, Esl2p, prohibitin) that provide a valuable resource for future investigations on the functionality, dynamics, and regulation of the peroxisomal importomer.

@article{oeljeklausIdentificationCoreComponents2012a, abstract = {The importomer complex plays an essential role in the biogenesis of peroxisomes by mediating the translocation of matrix proteins across the organellar membrane. A central part of this highly dynamic import machinery is the docking complex consisting of Pex14p, Pex13p, and Pex17p that is linked to the RING finger complex (Pex2p, Pex10p, Pex12p) via Pex8p. To gain detailed knowledge on the molecular players governing peroxisomal matrix protein import and, thus, the integrity and functionality of peroxisomes, we aimed at a most comprehensive investigation of stable and transient interaction partners of Pex14p, the central component of the importomer. To this end, we performed a thorough quantitative proteomics study based on epitope tagging of Pex14p combined with dual-track stable isotope labeling with amino acids in cell culture-mass spectrometry (SILAC-MS) analysis of affinity-purified Pex14p complexes and statistics. The results led to the establishment of the so far most extensive Pex14p interactome, comprising 9 core and further 12 transient components. We confirmed virtually all known Pex14p interaction partners including the core constituents of the importomer as well as Pex5p, Pex11p, Pex15p, and Dyn2p. More importantly, we identified new transient interaction partners (Pex25p, Hrr25p, Esl2p, prohibitin) that provide a valuable resource for future investigations on the functionality, dynamics, and regulation of the peroxisomal importomer.}, added-at = {2024-05-17T13:01:35.000+0200}, address = {United States}, author = {Oeljeklaus, Silke and Reinartz, Benedikt S. and Wolf, Janina and Wiese, Sebastian and Tonillo, Jason and Podwojski, Katharina and Kuhlmann, Katja and Stephan, Christian and Meyer, Helmut E. and Schliebs, Wolfgang and Brocard, C{\'e}cile and Erdmann, Ralf and Warscheid, Bettina}, biburl = {https://www.bibsonomy.org/bibtex/2a99c4458864245f3a9cb385155a6aa37/warscheidlab}, doi = {10.1021/pr3000333}, interhash = {211798749154765bdd2899352bd09452}, intrahash = {a99c4458864245f3a9cb385155a6aa37}, issn = {1535-3907 1535-3893}, journal = {Journal of proteome research}, keywords = {Acids/chemistry/metabolism,Chromatography Amino Design,Saccharomyces Fragments/analysis/chemistry/metabolism,Peroxisomes/*chemistry/metabolism,Protein High Interaction Labeling/*methods,Peptide Liquid,Isotope Maps,Proteomics/*methods,Research Mass Pressure Proteins/analysis/chemistry/metabolism,Saccharomyces Spectrometry,to_read cerevisiae cerevisiae/metabolism,Tandem}, langid = {english}, month = apr, number = 4, pages = {2567--2580}, pmid = {22375831}, timestamp = {2024-05-17T13:01:35.000+0200}, title = {Identification of Core Components and Transient Interactors of the Peroxisomal Importomer by Dual-Track Stable Isotope Labeling with Amino Acids in Cell Culture Analysis.}, volume = 11, year = 2012 }