Evidence map›Paper›PMID 33481336›Full record

ArticleBiotechnology journal2021

Generation of enzymatically competent SARS-CoV-2 decoy receptor ACE2-Fc in glycoengineered Nicotiana benthamiana.

Alexandra Castilho, Jennifer Schwestka, Nikolaus F Kienzl, Ulrike Vavra, Clemens Grünwald-Gruber, Shiva Izadi, Chaitra Hiremath, Janine Niederhöfer, Elisabeth Laurent, Vanessa Monteil and 6 more

Open access · hybridAbstract read
In one paragraph

Article in Biotechnology journal, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
4.5field-weighted citation impact, top 5% 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

25 citing papers in PubMed, 35 citations in OpenAlex.

  1. Review
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  11. Plant-based biopharmaceutical engineering.Nature reviews bioengineering · 2023
    Review
  12. Article
  13. Article
  14. Frontiers in bioengineering and biotechnology · 2023
    Article
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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

16 authors at 4 institutions in 3 countries.

Alexandra CastilhoDepartment of Applied Genetics and Cell Biology, Institute of Plant Biotechnology and Cell Biology, University of Natural Resources and Life Sciences Vienna, Vienna, Austria.
Jennifer SchwestkaDepartment of Applied Genetics and Cell Biology, Institute of Plant Biotechnology and Cell Biology, University of Natural Resources and Life Sciences Vienna, Vienna, Austria.
Nikolaus F KienzlDepartment of Applied Genetics and Cell Biology, Institute of Plant Biotechnology and Cell Biology, University of Natural Resources and Life Sciences Vienna, Vienna, Austria.ORCID https://orcid.org/0000-0001-8057-3930
Ulrike VavraDepartment of Applied Genetics and Cell Biology, Institute of Plant Biotechnology and Cell Biology, University of Natural Resources and Life Sciences Vienna, Vienna, Austria.
Clemens Grünwald-GruberDepartment of Chemistry, Institute of Biochemistry, University of Natural Resources and Life Sciences Vienna, Vienna, Austria.
Shiva IzadiDepartment of Applied Genetics and Cell Biology, Institute of Plant Biotechnology and Cell Biology, University of Natural Resources and Life Sciences Vienna, Vienna, Austria.
Chaitra HiremathDepartment of Applied Genetics and Cell Biology, Institute of Plant Biotechnology and Cell Biology, University of Natural Resources and Life Sciences Vienna, Vienna, Austria.
Janine NiederhöferApeiron Biologics AG, Campus Vienna Biocenter, Vienna, Austria.
Elisabeth LaurentDepartment of Biotechnology and Core Facility Biomolecular & Cellular Analysis, University of Natural Resources and Life Sciences Vienna, Vienna, Austria.ORCID https://orcid.org/0000-0002-5234-5524
Vanessa MonteilDepartment of Laboratory Medicine, Unit of Clinical Microbiology, Karolinska Institute and Karolinska University Hospital, Stockholm, Sweden.
Ali MirazimiDepartment of Laboratory Medicine, Unit of Clinical Microbiology, Karolinska Institute and Karolinska University Hospital, Stockholm, Sweden.
Gerald WirnsbergerApeiron Biologics AG, Campus Vienna Biocenter, Vienna, Austria.
Johannes StadlmannDepartment of Chemistry, Institute of Biochemistry, University of Natural Resources and Life Sciences Vienna, Vienna, Austria.
Eva StögerDepartment of Applied Genetics and Cell Biology, Institute of Plant Biotechnology and Cell Biology, University of Natural Resources and Life Sciences Vienna, Vienna, Austria.
Lukas MachDepartment of Applied Genetics and Cell Biology, Institute of Plant Biotechnology and Cell Biology, University of Natural Resources and Life Sciences Vienna, Vienna, Austria.ORCID https://orcid.org/0000-0001-9013-5408
Richard StrasserDepartment of Applied Genetics and Cell Biology, Institute of Plant Biotechnology and Cell Biology, University of Natural Resources and Life Sciences Vienna, Vienna, Austria.ORCID https://orcid.org/0000-0001-8764-6530
BOKU University · ATKarolinska University Hospital · SEVienna Biocenter · ATTarbiat Modares University · IR

Funding

Austrian Science Fund FWF P 31131Austrian Science Fund FWF P 31920Austrian Science Fund FWF W 1224
6 · The paper itself

Abstract

Human angiotensin-converting enzyme 2 (ACE2) is the primary host cell receptor for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) binding and cell entry. Administration of high concentrations of soluble ACE2 can be utilized as a decoy to block the interaction of the virus with cellular ACE2 receptors and potentially be used as a strategy for treatment or prevention of coronavirus disease 2019. Human ACE2 is heavily glycosylated and its glycans impact on binding to the SARS-CoV-2 spike protein and virus infectivity. Here, we describe the production of a recombinant soluble ACE2-fragment crystallizable (Fc) variant in glycoengineered Nicotiana benthamiana. Our data reveal that the produced dimeric ACE2-Fc variant is glycosylated with mainly complex human-type N-glycans and functional with regard to enzyme activity, affinity to the SARS-CoV-2 receptor-binding domain, and wild-type virus neutralization.

Indexed as

COVID-19SARS-CoV-2Angiotensin-Converting Enzyme 2HumansNicotianaPeptidyl-Dipeptidase AProtein BindingSpike Glycoprotein, CoronavirusAngiotensin-Converting Enzyme 2Peptidyl-Dipeptidase ASpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2COVID-19glycosylationposttranslational modificationrecombinant protein expressionSARS-CoV-2

Identifiers

PMID33481336
PMCPMC7995010
OpenAlexW3126144545

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.