Evidence map›Paper›PMID 27943242›Full record

ArticleBiotechnology and bioengineering2017

Knockout of a difficult-to-remove CHO host cell protein, lipoprotein lipase, for improved polysorbate stability in monoclonal antibody formulations.

Josephine Chiu, Kristin N Valente, Nicholas E Levy, Lie Min, Abraham M Lenhoff, Kelvin H Lee

Abstract read
In one paragraph

Article in Biotechnology and bioengineering, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
10.2field-weighted citation impact, top 1% 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

49 citing papers in PubMed, 202 citations in OpenAlex.

  1. Review
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  11. Analytical Tools for HCP Detection, Identification, and Quantitation.Methods in molecular biology (Clifton, N.J.) · 2025
    Article
  12. Article
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  16. Review
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  19. Article
  20. Oxidation of polysorbates - An underestimated degradation pathway?International journal of pharmaceutics: X · 2023
    Review
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

6 authors at 2 institutions in 1 country.

Josephine ChiuDepartment of Chemical and Biomolecular Engineering, University of Delaware, Newark, Delaware, 19716.
Kristin N ValenteDepartment of Chemical and Biomolecular Engineering, University of Delaware, Newark, Delaware, 19716.
Nicholas E LevyDepartment of Chemical and Biomolecular Engineering, University of Delaware, Newark, Delaware, 19716.
Lie MinDepartment of Chemical and Biomolecular Engineering, University of Delaware, Newark, Delaware, 19716.
Abraham M LenhoffDepartment of Chemical and Biomolecular Engineering, University of Delaware, Newark, Delaware, 19716.
Kelvin H LeeDepartment of Chemical and Biomolecular Engineering, University of Delaware, Newark, Delaware, 19716.
University of Delaware · USBiotechnology Institute · US

Funding

Predictive Modeling & Optimal Control Framework for Model-Based Epidemic Response in DelawareP20GM103446 · NIGMS · UNIVERSITY OF DELAWARE · PI Anjana Narayan Bhat · 2012 to 2026
$67.2M
CHEMISTRY-BIOLOGY INTERFACE PREDOCTORAL TRAININGT32GM008550 · NIGMS · UNIVERSITY OF DELAWARE · PI BAHNSON, BRIAN J · 1994 to 2018
$5.0M
NIGMS NIH HHS P20 GM103446NIGMS NIH HHS T32 GM008550
6 · The paper itself

Abstract

While the majority of host cell protein (HCP) impurities are effectively removed in typical downstream purification processes, a small population of HCPs are particularly challenging. Previous studies have identified HCPs that are challenging for a variety of reasons. Lipoprotein lipase (LPL)-a Chinese hamster ovary (CHO) HCP that functions to hydrolyze esters in triglycerides-was one of ten HCPs identified in previous studies as being susceptible to retention in downstream processing. LPL may degrade polysorbate 80 (PS-80) and polysorbate 20 (PS-20) in final product formulations due to the structural similarity between polysorbates and triglycerides. In this work, recombinant LPL was found to have enzymatic activity against PS-80 and PS-20 in a range of solution conditions that are typical of mAb formulations. LPL knockout CHO cells were created with CRISPR and TALEN technologies and resulting cell culture harvest fluid demonstrated significantly reduced polysorbate degradation without significant impact on cell viability when compared to wild-type samples. Biotechnol. Bioeng. 2017;114: 1006-1015. © 2016 Wiley Periodicals, Inc.

Indexed as

Gene Knockout TechniquesAnimalsAntibodies, MonoclonalCHO CellsCricetinaeCricetulusCRISPR-Cas SystemsDrug StabilityEscherichia coliGene EditingLipoprotein LipaseMetabolic EngineeringOleic AcidPolysorbatesAntibodies, MonoclonalLipoprotein LipaseOleic AcidPolysorbatesCHO cellCRISPRhost cell proteinlipasepolysorbate

Identifiers

PMID27943242
PMCPMC5360534
OpenAlexW2566325029

What OpenQuestion holds

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LicenceTDM
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.