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NonFullScreenPageMode: UseNone Direction: L2R ViewArea: CropBox ViewClip: CropBox PrintArea: CropBox PageClip: CropBox PageLayout: SinglePage PageMode: UseOutlines Language: en-US Outlines: Item: Title: Targeted knockdown of ATM, ATR, and PDEδ increases Gag HIV-1 VLP production in HEK293 cells Children: Item: Title: Abstract Item: Title: Key points Item: Title: Introduction Item: Title: Materials and methods Children: Item: Title: HEK293 mammalian cell line and culture conditions Item: Title: Transient transfection Item: Title: Design of experiments: Box-Behnken Item: Title: Flow cytometry Item: Title: Plasmids and shRNAs Item: Title: HIV-1 gag VLP quantification Children: Item: Title: Fluorimetry Item: Title: Nanoparticle tracking analysis Item: Title: Flow virometry Item: Title: Statistical analyses Item: Title: Western blots Item: Title: Bioreactor culture conditions and setup description Item: Title: Results Children: Item: Title: Knocking down ATM, ATR, and PDEδ increases VLP titers in the supernatant Item: Title: Assessment of key parameters of Gag VLP production revealed changes in VLP size distribution and secretion upon knockdown Item: Title: Analysis of the metabolic interactions between knockdowns reveals the pivotal role of ATM Item: Title: Intensification of the Gag VLP production process using a lab-scale stirred tank bioreactor operating in perfusion Item: Title: Discussion Children: Item: Title: Effect of knockdown strategies on VLP production in HEK293 cells Item: Title: Effect of the knockdowns on key production parameters Item: Title: Optimization of the metabolic interactions between the different knockdowns Item: Title: Implementation of the ATM knockdown in the EGE methodology Item: Title: Acknowledgements Item: Title: References Info: Title: Targeted knockdown of ATM, ATR, and PDEδ increases Gag HIV-1 VLP production in HEK293 cells Author: Andy Díaz-Maneh Subject: Applied Microbiology and Biotechnology, 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