Publikation: Expression and purification of the soluble isoform of human receptor for advanced glycation end products (sRAGE) from Pichia pastoris
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RAGE is a multi-ligand receptor involved in various human diseases including diabetes, cancer or Alzheimer's disease. Engagement of RAGE by its ligands triggers activation of key cellular signalling pathways such as the MAP kinase and NF-kappaB pathways. Whereas the main isoform of RAGE is a transmembrane receptor with both extra- and intracellular domains, a secreted soluble isoform (sRAGE), corresponding to the extracellular part only, has the ability to block RAGE signalling and suppress cellular activation. Administration of sRAGE to animal models of cancer or multiple sclerosis blocked successfully tumour growth and the course of the autoimmune disease. These findings demonstrate that sRAGE may have a potential as therapeutic. We present here a fast and simple purification protocol of sRAGE from the yeast Pichia pastoris. The identity of the protein was confirmed by mass spectrometry and Western blot. The protein was N-glycosylated and 95-98% pure as judged by SDS-PAGE.
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OSTENDORP, Thorsten, Mirjam WEIBEL, Estelle LECLERC, Peter KLEINERT, Peter M. H. KRONECK, Claus W. HEIZMANN, Günter FRITZ, 2006. Expression and purification of the soluble isoform of human receptor for advanced glycation end products (sRAGE) from Pichia pastoris. In: Biochemical and Biophysical Research Communications. 2006, 347(1), pp. 4-11. ISSN 0006-291X. eISSN 1090-2104. Available under: doi: 10.1016/j.bbrc.2006.04.077BibTex
@article{Ostendorp2006-08Expre-37283, year={2006}, doi={10.1016/j.bbrc.2006.04.077}, title={Expression and purification of the soluble isoform of human receptor for advanced glycation end products (sRAGE) from Pichia pastoris}, number={1}, volume={347}, issn={0006-291X}, journal={Biochemical and Biophysical Research Communications}, pages={4--11}, author={Ostendorp, Thorsten and Weibel, Mirjam and Leclerc, Estelle and Kleinert, Peter and Kroneck, Peter M. H. and Heizmann, Claus W. and Fritz, Günter} }
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