Streamlining homogeneous glycoprotein production for biophysical and structural applications by targeted cell line development.
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Authors
Wilke, SonjaGroebe, Lothar
Maffenbeier, Vitali
Jäger, Volker
Gossen, Manfred
Josewski, Jörn
Duda, Agathe
Polle, Lilia
Owens, Raymond J
Wirth, Dagmar
Heinz, Dirk W
van den Heuvel, Joop
Büssow, Konrad
Issue Date
2011
Metadata
Show full item recordAbstract
Studying the biophysical characteristics of glycosylated proteins and solving their three-dimensional structures requires homogeneous recombinant protein of high quality.We introduce here a new approach to produce glycoproteins in homogenous form with the well-established, glycosylation mutant CHO Lec3.2.8.1 cells. Using preparative cell sorting, stable, high-expressing GFP 'master' cell lines were generated that can be converted fast and reliably by targeted integration via Flp recombinase-mediated cassette exchange (RMCE) to produce any glycoprotein. Small-scale transient transfection of HEK293 cells was used to identify genetically engineered constructs suitable for constructing stable cell lines. Stable cell lines expressing 10 different proteins were established. The system was validated by expression, purification, deglycosylation and crystallization of the heavily glycosylated luminal domains of lysosome-associated membrane proteins (LAMP).Citation
Streamlining homogeneous glycoprotein production for biophysical and structural applications by targeted cell line development. 2011, 6 (12):e27829 PLoS ONEAffiliation
Department of Molecular Structural Biology, Helmholtz Centre for Infection Research, Braunschweig, Germany.Journal
PloS onePubMed ID
22174749Type
ArticleLanguage
enISSN
1932-6203ae974a485f413a2113503eed53cd6c53
10.1371/journal.pone.0027829
Scopus Count
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