Evidence map›Paper›PMID 26657798›Full record

ArticleScientific reports2015

Versatile microscale screening platform for improving recombinant protein productivity in Chinese hamster ovary cells.

Henning Gram Hansen, Claes Nymand Nilsson, Anne Mathilde Lund, Stefan Kol, Lise Marie Grav, Magnus Lundqvist, Johan Rockberg, Gyun Min Lee, Mikael Rørdam Andersen, Helene Faustrup Kildegaard

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.7field-weighted citation impact, top 16% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 29 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 3 institutions in 3 countries.

Henning Gram HansenThe Novo Nordisk Foundation Center for Biosustainability, Technical University of Denmark (DTU), Hørsholm, Denmark.
Claes Nymand NilssonThe Novo Nordisk Foundation Center for Biosustainability, Technical University of Denmark (DTU), Hørsholm, Denmark.
Anne Mathilde LundDepartment of Systems Biology, Technical University of Denmark (DTU), Lyngby, Denmark.
Stefan KolThe Novo Nordisk Foundation Center for Biosustainability, Technical University of Denmark (DTU), Hørsholm, Denmark.
Lise Marie GravThe Novo Nordisk Foundation Center for Biosustainability, Technical University of Denmark (DTU), Hørsholm, Denmark.
Magnus LundqvistDepartment of Proteomics and Nanobiotechnology, Royal Institute of Technology (KTH), Stockholm, Sweden.
Johan RockbergDepartment of Proteomics and Nanobiotechnology, Royal Institute of Technology (KTH), Stockholm, Sweden.
Gyun Min LeeThe Novo Nordisk Foundation Center for Biosustainability, Technical University of Denmark (DTU), Hørsholm, Denmark.
Mikael Rørdam AndersenDepartment of Systems Biology, Technical University of Denmark (DTU), Lyngby, Denmark.
Helene Faustrup KildegaardThe Novo Nordisk Foundation Center for Biosustainability, Technical University of Denmark (DTU), Hørsholm, Denmark.
Technical University of Denmark · DKNovo Nordisk Foundation · DKKTH Royal Institute of Technology · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chinese hamster ovary (CHO) cells are widely used as cell factories for the production of biopharmaceuticals. In contrast to the highly optimized production processes for monoclonal antibody (mAb)-based biopharmaceuticals, improving productivity of non-mAb therapeutic glycoproteins is more likely to reduce production costs significantly. The aim of this study was to establish a versatile target gene screening platform for improving productivity for primarily non-mAb glycoproteins with complete interchangeability of model proteins and target genes using transient expression. The platform consists of four techniques compatible with 96-well microplates: lipid-based transient transfection, cell cultivation in microplates, cell counting and antibody-independent product titer determination based on split-GFP complementation. We were able to demonstrate growth profiles and volumetric productivity of CHO cells in 96-half-deepwell microplates comparable with those obtained in shake flasks. In addition, we demonstrate that split-GFP complementation can be used to accurately measure relative titers of therapeutic glycoproteins. Using this platform, we were able to detect target gene-specific increase in titer and specific productivity of two non-mAb glycoproteins. In conclusion, the platform provides a novel miniaturized and parallelisable solution for screening target genes and holds the potential to unravel genes that can enhance the secretory capacity of CHO cells.

Indexed as

Cell Culture TechniquesHigh-Throughput Screening AssaysAnimalsCHO CellsCricetinaeCricetulusEnzyme-Linked Immunosorbent AssayGene ExpressionGenes, ReporterGlycosylationProtein Interaction Domains and MotifsRecombinant Fusion ProteinsRecombinant ProteinsReproducibility of ResultsRecombinant Fusion ProteinsRecombinant Proteins

Identifiers

PMID26657798
PMCPMC4676018
OpenAlexW2333143137

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.