Development of an efficient method for selection of stable cell pools for protein expression and surface display with Expi293F cells

Author:

Chen Chuan1ORCID,Wang Zening2,Sun Zehua13,Li Wei1,Dimitrov Dimiter S.13

Affiliation:

1. Division of Infectious Diseases, Department of Medicine, Center for Antibody Therapeutics University of Pittsburgh Medical School Pittsburgh Pennsylvania USA

2. Institute of Molecular Medicine University of Texas Health Science Center at Houston Houston Texas USA

3. Abound Bio Pittsburgh Pennsylvania USA

Abstract

AbstractCompare with transient expression, stable cell lines generally have higher productivity and better quality for protein expression. However, selection of stable cell line is time‐consuming and laborious. Here we describe an optimized selection method to achieve high‐efficient stable cell pools with Expi293F suspension cells. This method only takes 2–3 weeks to generate stable cell pools with 2‐ to 10‐fold higher productivity than transient gene expression (TGE). In fed‐batch culture with Yeastolate, >1 g/L yield was achieved with our KTN0239‐IgG stable cell pool in shaker flasks. This method can be also applied to efficiently display proteins on the cell surface.

Funder

University of Pittsburgh

Publisher

Wiley

Subject

Cell Biology,Clinical Biochemistry,General Medicine,Biochemistry

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