Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/168601
Title: A versatile genomic transgenesis platform with enhanced λ integrase for human Expi293F cells
Authors: Siddiqui, Asim Azhar
Peter, Sabrina
Ngoh, Eve Zi Xian
Wang, Cheng-I
Ng, Shirelle
Dangerfield, John A.
Gunzburg, Walter H.
Dröge, Peter
Makhija, Harshyaa
Keywords: Science
Issue Date: 2023
Source: Siddiqui, A. A., Peter, S., Ngoh, E. Z. X., Wang, C., Ng, S., Dangerfield, J. A., Gunzburg, W. H., Dröge, P. & Makhija, H. (2023). A versatile genomic transgenesis platform with enhanced λ integrase for human Expi293F cells. Frontiers in Bioengineering and Biotechnology, 11, 1198465-. https://dx.doi.org/10.3389/fbioe.2023.1198465
Project: NRF-CRP21-2018-0002 
Journal: Frontiers in Bioengineering and Biotechnology 
Abstract: Reliable cell-based platforms to test and/or produce biologics in a sustainable manner are important for the biotech industry. Utilizing enhanced λ integrase, a sequence-specific DNA recombinase, we developed a novel transgenesis platform involving a fully characterized single genomic locus as an artificial landing pad for transgene insertion in human Expi293F cells. Importantly, transgene instability and variation in expression were not observed in the absence of selection pressure, thus enabling reliable long-term biotherapeutics testing or production. The artificial landing pad for λ integrase can be targeted with multi-transgene constructs and offers future modularity involving additional genome manipulation tools to generate sequential or nearly seamless insertions. We demonstrated broad utility with expression constructs for anti PD-1 monoclonal antibodies and showed that the orientation of heavy and light chain transcription units profoundly affected antibody expression levels. In addition, we demonstrated encapsulation of our PD-1 platform cells into bio-compatible mini-bioreactors and the continued secretion of antibodies, thus providing a basis for future cell-based 32 applications for more effective and affordable therapies.
URI: https://hdl.handle.net/10356/168601
ISSN: 2296-4185
DOI: 10.3389/fbioe.2023.1198465
Schools: School of Biological Sciences 
Organisations: Singapore Immunology Network, A*STAR 
Rights: © 2023 Siddiqui, Peter, Ngoh, Wang, Ng, Dangerfield, Gunzburg, Dröge and Makhija. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
Fulltext Permission: open
Fulltext Availability: With Fulltext
Appears in Collections:SBS Journal Articles

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