Evidence map›Paper›PMID 31087560›Full record

ArticleBiotechnology and bioengineering2019

Identification and CRISPR/Cas9 Inactivation of the C1s Protease Responsible for Proteolysis of Recombinant Proteins Produced in CHO Cells.

Sophia W Li, Bin Yu, Gabriel Byrne, Meredith Wright, Sara O'Rourke, Kathryn Mesa, Phillip W Berman

Open access · greenAbstract read
In one paragraph

Article in Biotechnology and bioengineering, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.8field-weighted citation impact, top 17% 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

12 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
  2. Analytical Tools for HCP Detection, Identification, and Quantitation.Methods in molecular biology (Clifton, N.J.) · 2025
    Article
  3. Review
  4. Comparative RNA-Seq of TenMarine drugs · 2024
    Article
  5. Review
  6. Review
  7. Review
  8. CRISPR Technologies in Chinese Hamster Ovary Cell Line Engineering.International journal of molecular sciences · 2023
    Review
  9. Recombinant Protein Production and Purification of Insoluble Proteins.Methods in molecular biology (Clifton, N.J.) · 2022
    Article
  10. Article
  11. Article
  12. 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

7 authors at 1 institution in 1 country.

Sophia W LiDepartment of Chemistry, University of California Santa Cruz, California.
Bin YuDepartment of Biomolecular Engineering, University of California Santa Cruz, California.
Gabriel ByrneDepartment of Biomolecular Engineering, University of California Santa Cruz, California.
Meredith WrightDepartment of Biomolecular Engineering, University of California Santa Cruz, California.
Sara O'RourkeDepartment of Biomolecular Engineering, University of California Santa Cruz, California.
Kathryn MesaDepartment of Biomolecular Engineering, University of California Santa Cruz, California.
Phillip W BermanDepartment of Biomolecular Engineering, University of California Santa Cruz, California.
University of California, Santa Cruz · US

Funding

Enhanced Anti-HIV-1 Antibody Responses in African American Women Seropositive forR01DA036335 · NIDA · UNIVERSITY OF CALIFORNIA SANTA CRUZ · PI BERMAN, PHILLIP WAYNE · 2013 to 2017
$3.0M
NIDA NIH HHS R01 DA036335
6 · The paper itself

Abstract

Proteolysis associated with recombinant protein expression in Chinese Hamster Ovary (CHO) cells has hindered the development of biologics including HIV vaccines. When expressed in CHO cells, the recombinant HIV envelope protein, gp120, undergoes proteolytic clipping by a serine protease at a key epitope recognized by neutralizing antibodies. The problem is particularly acute for envelope proteins from clade B viruses that represent the major genetic subtype circulating in much of the developed world, including the US and Europe. In this paper, we have identified complement Component 1's (C1s), a serine protease from the complement cascade, as the protease responsible for the proteolysis of gp120 in CHO cells. CRISPR/Cas9 knockout of the C1s protease in a CHO cell line was shown to eliminate the proteolytic activity against the recombinantly expressed gp120. In addition, the C1s

Indexed as

CRISPR-Cas SystemsGene Knockout TechniquesHIV-1ProteolysisAnimalsCHO CellsComplement C1sCricetulusHIV Envelope Protein gp120Recombinant ProteinsComplement C1sgp120 protein, Human immunodeficiency virus 1HIV Envelope Protein gp120Recombinant ProteinsC1sCell engineeringCHO cellsCRISPR/cas9Env Proteingene editingglycosylationHIVMGAT1proteasevaccine

Identifiers

PMID31087560
PMCPMC6675663
OpenAlexW2945769754

What OpenQuestion holds

Textmetadata
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.