Evidence map›Paper›PMID 35405107›Full record

ArticleJournal of molecular biology2022

Development of Monoclonal Antibodies to Detect for SARS-CoV-2 Proteins.

Nawneet Mishra, Joan Teyra, RuthMabel Boytz, Shane Miersch, Trudy N Merritt, Lia Cardarelli, Maryna Gorelik, Filip Mihalic, Per Jemth, Robert A Davey and 3 more

Open access · greenAbstract read
In one paragraph

Article in Journal of molecular biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 37% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. 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

13 authors at 4 institutions in 3 countries.

Nawneet MishraDepartment of Pathology and Immunology, Washington University School of Medicine in St Louis, St Louis, MO 63110, USA.
Joan TeyraThe Donnelly Centre, University of Toronto, Toronto, Canada.
RuthMabel BoytzDepartment of Microbiology, Boston University School of Medicine, Boston, MA 02118, USA.
Shane MierschThe Donnelly Centre, University of Toronto, Toronto, Canada.
Trudy N MerrittDepartment of Medicine, Washington University School of Medicine, St Louis, MO 63110, USA.
Lia CardarelliThe Donnelly Centre, University of Toronto, Toronto, Canada.
Maryna GorelikThe Donnelly Centre, University of Toronto, Toronto, Canada.
Filip MihalicDepartment of Medical Biochemistry and Microbiology, Uppsala University, BMC Box 582, Husargatan 3, 751 23 Uppsala, Sweden.
Per JemthDepartment of Medical Biochemistry and Microbiology, Uppsala University, BMC Box 582, Husargatan 3, 751 23 Uppsala, Sweden.
Robert A DaveyDepartment of Microbiology, Boston University School of Medicine, Boston, MA 02118, USA.
Sachdev S SidhuThe Donnelly Centre, University of Toronto, Toronto, Canada.
Daisy W LeungDepartment of Medicine, Washington University School of Medicine, St Louis, MO 63110, USA.
Gaya K AmarasingheDepartment of Pathology and Immunology, Washington University School of Medicine in St Louis, St Louis, MO 63110, USA. Electronic address: gamarasinghe@wustl.edu.
University of Toronto · CAWashington University in St. Louis · USBoston University · USUppsala University · SE

Funding

Virology BSL4 CoreP01AI120943 · NIAID · WASHINGTON UNIVERSITY · PI Gaya K. Amarasinghe · 2016 to 2026
$30.2M
Mechanisms of actin cytoskeleton modulation by PneumovirusesR01AI140758 · NIAID · UNIVERSITY OF KENTUCKY · PI DUTCH, REBECCA E., LEUNG, DAISY W · 2018 to 2022
$3.3M
Development and characterization of engineered therapeutic antibodies against SARS-CoV-2R01AI161374 · NIAID · WASHINGTON UNIVERSITY · PI AMARASINGHE, GAYA K. · 2021 to 2023
$2.7M
NIAID NIH HHS P01 AI120943NIAID NIH HHS R01 AI140758NIAID NIH HHS R01 AI161374
6 · The paper itself

Abstract

The COVID-19 pandemic caused by SARS-CoV-2 infection has impacted the world economy and healthcare infrastructure. Key reagents with high specificity to SARS-CoV-2 proteins are currently lacking, which limits our ability to understand the pathophysiology of SARS-CoV-2 infections. To address this need, we initiated a series of studies to generate and develop highly specific antibodies against proteins from SARS-CoV-2 using an antibody engineering platform. These efforts resulted in 18 monoclonal antibodies against nine SARS-CoV-2 proteins. Here we report the characterization of several antibodies, including those that recognize Nsp1, Nsp8, Nsp12, and Orf3b viral proteins. Our validation studies included evaluation for use of antibodies in ELISA, western blots, and immunofluorescence assays (IFA). We expect that availability of these antibodies will enhance our ability to further characterize host-viral interactions, including specific roles played by viral proteins during infection, to acquire a better understanding of the pathophysiology of SARS-CoV-2 infections.

Indexed as

Antibodies, MonoclonalAntibodies, ViralCOVID-19SARS-CoV-2Viral ProteinsCell Surface Display TechniquesCoronavirus RNA-Dependent RNA PolymeraseEnzyme-Linked Immunosorbent AssayHumansViral Nonstructural ProteinsAntibodies, MonoclonalAntibodies, ViralCoronavirus RNA-Dependent RNA PolymeraseNS8 protein, SARS-CoV-2NSP12 protein, SARS-CoV-2ORF1ab polyprotein, SARS-CoV-2ORF3d protein, SARS-CoV2 virusViral Nonstructural ProteinsViral Proteinsantibodyphage displaySARS-CoV-2

Identifiers

PMID35405107
PMCPMC8993412
OpenAlexW4223534236

What OpenQuestion holds

Textmetadata
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.