Evidence map›Paper›PMID 33898396›Full record

ArticleFrontiers in bioengineering and biotechnology2021

Proteomic Profiling of IgG1 Producing CHO Cells Using LC/LC-SPS-MS

Lisa Strasser, Amy Farrell, Jenny T C Ho, Kai Scheffler, Ken Cook, Patrick Pankert, Peter Mowlds, Rosa Viner, Barry L Karger, Jonathan Bones

Open access · goldAbstract read
In one paragraph

Article in Frontiers in bioengineering and biotechnology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.0field-weighted citation impact, top 26% 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

6 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Proteomic Landscape of Adeno-Associated Virus (AAV)-Producing HEK293 Cells.International journal of molecular sciences · 2021
    Article
  6. Article
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 6 institutions in 4 countries.

Lisa StrasserCharacterization and Comparability Laboratory, National Institute for Bioprocessing Research and Training, Dublin, Ireland.
Amy FarrellCharacterization and Comparability Laboratory, National Institute for Bioprocessing Research and Training, Dublin, Ireland.
Jenny T C HoThermo Fisher Scientific, Hemel Hempstead, United Kingdom.
Kai SchefflerThermo Fisher Scientific, Germering, Germany.
Ken CookThermo Fisher Scientific, Hemel Hempstead, United Kingdom.
Patrick PankertThermo Fisher Scientific, Dreieich, Germany.
Peter MowldsThermo Fisher Scientific, Hemel Hempstead, United Kingdom.
Rosa VinerThermo Fisher Scientific, San Jose, CA, United States.
Barry L KargerBarnett Institute of Chemical and Biological Analysis, Northeastern University, Boston, MA, United States.
Jonathan BonesSchool of Chemical and Bioprocess Engineering, University College Dublin, Dublin, Ireland.
Thermo Fisher Scientific (United Kingdom) · GBNational Institute for Bioprocessing Research and Training · IEThermo Fisher Scientific (Germany) · DENortheastern University · USThermo Fisher Scientific (United States) · USUniversity College Dublin · IE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The biopharmaceutical market is dominated by monoclonal antibodies, the majority of which are produced in Chinese hamster ovary (CHO) cell lines. Intense cell engineering, in combination with optimization of various process parameters results in increasing product titers. To enable further improvements in manufacturing processes, detailed information about how certain parameters affect cellular mechanisms in the production cells, and thereby also the expressed drug substance, is required. Therefore, in this study the effects of commonly applied changes in bioprocessing parameters on an anti-IL8 IgG1 producing CHO DP-12 cell line were investigated on the level of host cell proteome expression combined with product quality assessment of the expressed IgG1 monoclonal antibody. Applying shifts in temperature, pH and dissolved oxygen concentration, respectively, resulted in altered productivity and product quality. Furthermore, analysis of the cells using two-dimensional liquid chromatography-mass spectrometry employing tandem mass tag based isotopic quantitation and synchronous precursor selection-MS

Indexed as

bioprocess monitoringCHO cellsmonoclonal antibodyprotein characterizationproteomic profilingSPS-MS3TMT

Identifiers

PMID33898396
PMCPMC8062983
OpenAlexW3153500354

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.