例如:"lncRNA", "apoptosis", "WRKY"

Proteomic mapping by rapamycin-dependent targeting of APEX2 identifies binding partners of VAPB at the inner nuclear membrane.

J Biol Chem. 2019 Nov 01;294(44):16241-16254. Epub 2019 Sep 13
Christina James 1 , Marret Müller 1 , Martin W Goldberg 2 , Christof Lenz 3 , Henning Urlaub 3 , Ralph H Kehlenbach 4
Christina James 1 , Marret Müller 1 , Martin W Goldberg 2 , Christof Lenz 3 , Henning Urlaub 3 , Ralph H Kehlenbach 4
+ et al

[No authors listed]

Author information
  • 1 Department of Molecular Biology, Faculty of Medicine, Göttingen Center for Molecular Biosciences (GZMB), Georg August University Göttingen, Humboldtallee 23, 37073 Göttingen, Germany.
  • 2 School of Biological and Biomedical Sciences, Durham University, Durham DH1 3LE, United Kingdom.
  • 3 Bioanalytical Mass Spectrometry Group, Max Planck Institute for Biophysical Chemistry, Am Fassberg 11, 37077 Göttingen, Germany.
  • 4 Department of Molecular Biology, Faculty of Medicine, Göttingen Center for Molecular Biosciences (GZMB), Georg August University Göttingen, Humboldtallee 23, 37073 Göttingen, Germany rkehlen@gwdg.de.

摘要


Vesicle-associated membrane protein-associated protein B (VAPB) is a tail-anchored protein that is present at several contact sites of the endoplasmic reticulum (ER). We now show by immunoelectron microscopy that VAPB also localizes to the inner nuclear membrane (INM). Using a modified enhanced ascorbate peroxidase 2 (APEX2) approach with rapamycin-dependent targeting of the peroxidase to a protein of interest, we searched for proteins that are in close proximity to VAPB, particularly at the INM. In combination with stable isotope labeling with amino acids in cell culture (SILAC), we confirmed many well-known interaction partners at the level of the ER with a clear distinction between specific and nonspecific hits. Furthermore, we identified emerin, TMEM43, and ELYS as potential interaction partners of VAPB at the INM and the nuclear pore complex, respectively.

KEYWORDS: APEX, RAPIDS, VAPB, biotin, emerin, endoplasmic reticulum (ER), nuclear envelope, nuclear pore, peroxidase, proteomic proximity mapping