Literature DB >> 24704608

Development of a semi-automated high throughput transient transfection system.

Aaron B Bos1, Joseph N Duque1, Sunil Bhakta2, Farzam Farahi3, Lindsay A Chirdon4, Jagath R Junutula2, Peter D Harms4, Athena W Wong5.   

Abstract

Transient transfection of mammalian cells provides a rapid method of producing protein for research purposes. Combining the transient transfection protein expression system with new automation technologies developed for the biotechnology industry would enable a high throughput protein production platform that could be utilized to generate a variety of different proteins in a short amount of time. These proteins could be used for an assortment of studies including proof of concept, antibody development, and biological structure and function. Here we describe such a platform: a semi-automated process for PEI-mediated transient protein production in tubespins at a throughput of 96 transfections at a time using a Biomek FX(P) liquid handling system. In one batch, 96 different proteins can be produced in milligram amounts by PEI transfection of HEK293 cells cultured in 50 mL tubespins. Methods were developed for the liquid handling system to automate the different processes associated with transient transfections such as initial cell seeding, DNA:PEI complex activation and DNA:PEI complex addition to the cells. Increasing DNA:PEI complex incubation time resulted in lower protein expression. To minimize protein production variability, the methods were further optimized to achieve consistent cell seeding, control the DNA:PEI incubation time and prevent cross-contamination among different tubespins. This semi-automated transfection process was applied to express 520 variants of a human IgG1 (hu IgG1) antibody. Published by Elsevier B.V.

Entities:  

Keywords:  Automation; HEK293T; Protein expression; Transient transfection; Tubespins

Mesh:

Substances:

Year:  2014        PMID: 24704608     DOI: 10.1016/j.jbiotec.2014.03.027

Source DB:  PubMed          Journal:  J Biotechnol        ISSN: 0168-1656            Impact factor:   3.307


  11 in total

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Journal:  Antib Ther       Date:  2022-01-10

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Journal:  Protein Eng Des Sel       Date:  2017-09-01       Impact factor: 1.650

10.  High-resolution glycosylation site-engineering method identifies MICA epitope critical for shedding inhibition activity of anti-MICA antibodies.

Authors:  T Noelle Lombana; Marissa L Matsumoto; Amy M Berkley; Evangeline Toy; Ryan Cook; Yutian Gan; Changchun Du; Paul Schnier; Wendy Sandoval; Zhengmao Ye; Jill M Schartner; Jeong Kim; Christoph Spiess
Journal:  MAbs       Date:  2018-11-22       Impact factor: 5.857

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