<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Budge JD</submitter><funding>Biotechnology and Biological Sciences Research Council</funding><pagination>679448</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8212061</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>9</volume><pubmed_abstract>Transient gene expression (TGE) in mammalian cells is a method of rapidly generating recombinant protein material for initial characterisation studies that does not require time-consuming processes associated with stable cell line construction. High TGE yields are heavily dependent on efficient delivery of plasmid DNA across both the plasma and nuclear membranes. Here, we harness the protein nucleoside diphosphate kinase (NDPK-A) that contains a nuclear localisation signal (NLS) to enhance DNA delivery into the nucleus of CHO cells. We show that co-expression of NDPK-A during transient expression results in improved transfection efficiency in CHO cells, presumably due to enhanced transportation of plasmid DNA into the nucleus via the nuclear pore complex. Furthermore, introduction of the E</pubmed_abstract><journal>Frontiers in bioengineering and biotechnology</journal><pubmed_title>Engineering of Chinese Hamster Ovary Cells With NDPK-A to Enhance DNA Nuclear Delivery Combined With EBNA1 Plasmid Maintenance Gives Improved Exogenous Transient Reporter, mAb and SARS-CoV-2 Spike Protein Expression.</pubmed_title><pmcid>PMC8212061</pmcid><funding_grant_id>BB/N023501/1</funding_grant_id><funding_grant_id>BB/V011324/1</funding_grant_id><pubmed_authors>Young RJ</pubmed_authors><pubmed_authors>Smales CM</pubmed_authors><pubmed_authors>Budge JD</pubmed_authors></additional><is_claimable>false</is_claimable><name>Engineering of Chinese Hamster Ovary Cells With NDPK-A to Enhance DNA Nuclear Delivery Combined With EBNA1 Plasmid Maintenance Gives Improved Exogenous Transient Reporter, mAb and SARS-CoV-2 Spike Protein Expression.</name><description>Transient gene expression (TGE) in mammalian cells is a method of rapidly generating recombinant protein material for initial characterisation studies that does not require time-consuming processes associated with stable cell line construction. High TGE yields are heavily dependent on efficient delivery of plasmid DNA across both the plasma and nuclear membranes. Here, we harness the protein nucleoside diphosphate kinase (NDPK-A) that contains a nuclear localisation signal (NLS) to enhance DNA delivery into the nucleus of CHO cells. We show that co-expression of NDPK-A during transient expression results in improved transfection efficiency in CHO cells, presumably due to enhanced transportation of plasmid DNA into the nucleus via the nuclear pore complex. Furthermore, introduction of the E</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021</publication><modification>2026-04-08T06:40:03.226Z</modification><creation>2022-02-10T15:48:35.047Z</creation></dates><accession>S-EPMC8212061</accession><cross_references><pubmed>34150735</pubmed><doi>10.3389/fbioe.2021.679448</doi></cross_references></HashMap>