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filingDate 2000-12-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2004-06-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_53550a7a66ab0ef8ce23e017f9a2f507
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publicationDate 2004-06-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber DK-175109-B1
titleOfInvention Method for activating gene-technologically prepared heterologous disulfide bridges containing eukaryotic proteins after expression in prokaryotic cells
abstract Method for activating non-glycosylated tissue plasminogen activator (t-PA) after its expression in prokaryotic cells comprises cell lysis; solubilisation under denaturing and reducing conditions, and reactivation under oxidising conditions in presence of reduced and oxidised glutathione (G5H, G55G). The new feature is that in the last stage is at pH 9-12 (pref. 9.5-11) with G5H and G55G concns. 0.1-20, pref. 0.2-10, mM and 0.01-3, pref. 0.5-1, mM, respectively, and with a non-denaturing concn. of the denaturing agent. Esp. the method is applied to t-PA expressed in E.coli and P. putida. The denaturing agent is pref. arginine, guanidine hydrochloride (both at 0.1-1, esp. 0.25-0.75, mM) or urea, at 0.5-4 (esp. 1-3.5) M in the last stage.
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