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Development of mammalian production cell lines expressing CNTO736, a glucagon like peptide‐1‐MIMETIBODYTM: Factors that influence productivity and product quality
Authors:Haimanti Dorai  Jennifer F. Nemeth  Erwin Cammaart  Yonghui Wang  Qing Mike Tang  Allen Magill  Michael J. Lewis  T. Shantha Raju  Kristen Picha  Karyn O'Neil  Subinay Ganguly  Gordon Moore
Affiliation:1. Centocor R&D, 145 King of Prussia Road, Radnor, Pennsylvania 19087;2. telephone: 610‐651‐7457;3. fax: 610‐993‐7842
Abstract:In an attempt to develop a high producing mammalian cell line expressing CNTO736, a Glucagon like peptide‐1‐antibody fusion protein (also known as a Glucagon like peptide‐1 MIMETIBODYTM), we have noted that the N‐terminal GLP‐1 portion of the MIMETIBODYTM was susceptible to proteolytic degradation during cell culture, which resulted in an inactive product. Therefore, a number of parameters that had an effect on productivity as well as product quality were examined. Results suggest that the choice of the host cell line had a significant effect on the overall product quality. Product expressed in mouse myeloma host cell lines had a lesser degree of proteolytic degradation and variability in O‐linked glycosylation as compared to that expressed in CHO host cell lines. The choice of a specific CHOK1SV derived clone also had an effect on the product quality. In general, molecules that exhibited minimal N‐terminal clipping had increased level of O‐linked glycosylation in the linker region, giving credence to the hypothesis that O‐linked glycosylation acts to protect against proteolytic degradation. Moreover, products with reduced potential for N‐terminal clipping had longer in vivo serum half‐life. These findings suggest that early monitoring of product quality should be an essential part of production cell line development and therefore, has been incorporated in our process of cell line development for this class of molecules. Biotechnol. Bioeng. 2009;103: 162–176. © 2008 Wiley Periodicals, Inc.
Keywords:MIMETIBODYTM  mammalian expression  N‐terminal clipping  mass spectrometry  CHO  NS0  HEK‐293  mammalian glycosylation
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