Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Julia Rosenlöcher"'
Autor:
Julia Rosenlöcher, Verena Böhrsch, Michael Sacharjat, Véronique Blanchard, Christoph Giese, Volker Sandig, Christian P. R. Hackenberger, Stephan Hinderlich
Publikováno v:
Bioengineering, Vol 2, Iss 4, Pp 213-234 (2015)
Manipulations of cell surface glycosylation or glycan decoration of selected proteins hold immense potential for exploring structure-activity relations or increasing glycoprotein quality. Metabolic glycoengineering describes the strategy where exogen
Externí odkaz:
https://doaj.org/article/b876e37c4dee42e2967b6abfacb50ab4
Publikováno v:
BioChem
Volume 1
Issue 2
Pages 8-97
Volume 1
Issue 2
Pages 8-97
The α-Gal epitope is an immunogen trisaccharide structure consisting of N-acetylglucosamine (GlcNAc)β1,4-galactose (Gal)α1,3-Gal. It is presented as part of complex-type glycans on glycoproteins or glycolipids on cell surfaces of non-primate mamma
Autor:
Christoph Kannicht, Philipp Wiedemann, Markus Krieger, Paul Rennert, Guido Kohla, Julia Rosenlöcher, Anja Brehm, Madeleine Peschke, Rico Uhler, Mathias Hafner, Annegrit Seifried, Ruth Popa-Wagner, Mario Kröning
Publikováno v:
Glycobiology. 31(7)
N-glycosylated proteins produced in human embryonic kidney 293 (HEK 293) cells often carry terminal N-acetylgalactosamine (GalNAc) and only low levels of sialylation. On therapeutic proteins, such N-glycans often trigger rapid clearance from the pati
Autor:
Stefan O. Reinke, Grit Sandig, Constanze Weilandt, Julia Rosenlöcher, Véronique Blanchard, Stephan Hinderlich
Publikováno v:
Protein Expression and Purification. 115:83-94
The market of therapeutic glycoproteins (including coagulation factors, antibodies, cytokines and hormones) is one of the profitable, fast-growing and challenging sectors of the biopharmaceutical industry. Although mammalian cell culture is still exp
Publikováno v:
Bioengineering
Bioengineering; Volume 4; Issue 2; Pages: 44
Bioengineering; Volume 4; Issue 2; Pages: 44
Prevention and treatment of bleeding in patients suffering from hemophilia A are inconvenient due to repeated intravenous infusions owing to the short half-life of coagulation factor VIII (FVIII) in circulation. Besides (glyco-)pegylation of the FVII