| Literature DB >> 30898338 |
Jae Seong Lee1, Helene Faustrup Kildegaard2, Nathan E Lewis3, Gyun Min Lee4.
Abstract
Mammalian expression platforms are primary production systems for therapeutic proteins that require complex post-translational modifications. Current processes used for developing recombinant mammalian cell lines generate clonal cell lines with high phenotypic heterogeneity, which has puzzled researchers that use mammalian cell culture systems for a long time. Advances in mammalian genome-editing technologies and systems biotechnology have shed light on clonal variation and enabled rational cell engineering in a targeted manner. We propose a new approach for a next-generation cell line development platform that can minimize clonal variation. Combined with the knowledge-based selection of ideal integration sites and engineering targets, targeted integration-based cell line development will allow tailored control of recombinant gene expression with predicted phenotypes.Entities:
Keywords: cell line development; clonal variation; rational cell engineering; transgene integration
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Year: 2019 PMID: 30898338 DOI: 10.1016/j.tibtech.2019.02.007
Source DB: PubMed Journal: Trends Biotechnol ISSN: 0167-7799 Impact factor: 19.536