Evidence map›Paper›PMID 35018379›Full record

ArticlebioRxiv : the preprint server for biology2021

Molecular probes of spike ectodomain and its subdomains for SARS-CoV-2 variants, Alpha through Omicron.

I-Ting Teng, Alexandra F Nazzari, Misook Choe, Tracy Liu, Matheus Oliveira de Souza, Yuliya Petrova, Yaroslav Tsybovsky, Shuishu Wang, Baoshan Zhang, Mykhaylo Artamonov and 11 more

Open access · greenAbstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
–field-weighted citation impact
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

19 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Genome-wide association studies dissect low-phosphorus stress response genes underling field and seedling traits in maize.TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · 2024
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  3. Exploring the phosphorus-starch content balance mechanisms in maize grains using GWAS population and transcriptome data.TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · 2024
    Article
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  9. Themis suppresses the effector function of CD8Cellular & molecular immunology · 2023
    Article
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  13. Prediction of Neurodevelopmental Disorders Based on De Novo Coding Variation.Journal of autism and developmental disorders · 2023
    Article
  14. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

21 authors at 3 institutions in 1 country.

I-Ting TengVaccine Research Center, National Institute of Allergy and Infectious Diseases, Bethesda, Maryland, United States of America.
Alexandra F NazzariVaccine Research Center, National Institute of Allergy and Infectious Diseases, Bethesda, Maryland, United States of America.
Misook ChoeVaccine Research Center, National Institute of Allergy and Infectious Diseases, Bethesda, Maryland, United States of America.
Tracy LiuVaccine Research Center, National Institute of Allergy and Infectious Diseases, Bethesda, Maryland, United States of America.
Matheus Oliveira de SouzaDepartment of Pharmaceutical Chemistry, The University of Kansas, Lawrence, Kansas, United States of America.
Yuliya PetrovaVaccine Research Center, National Institute of Allergy and Infectious Diseases, Bethesda, Maryland, United States of America.
Yaroslav TsybovskyElectron Microscopy Laboratory, Cancer Research Technology Program, Frederick National Laboratory for Cancer Research sponsored by the National Cancer Institute, Frederick, Maryland, United States of America.
Shuishu WangVaccine Research Center, National Institute of Allergy and Infectious Diseases, Bethesda, Maryland, United States of America.
Baoshan ZhangVaccine Research Center, National Institute of Allergy and Infectious Diseases, Bethesda, Maryland, United States of America.
Mykhaylo ArtamonovVaccine Research Center, National Institute of Allergy and Infectious Diseases, Bethesda, Maryland, United States of America.
Bharat MadanDepartment of Pharmaceutical Chemistry, The University of Kansas, Lawrence, Kansas, United States of America.
Aric HuangDepartment of Pharmaceutical Chemistry, The University of Kansas, Lawrence, Kansas, United States of America.
Sheila N Lopez AcevedoDepartment of Pharmaceutical Chemistry, The University of Kansas, Lawrence, Kansas, United States of America.
Xiaoli PanDepartment of Pharmaceutical Chemistry, The University of Kansas, Lawrence, Kansas, United States of America.
Tracy J RuckwardtVaccine Research Center, National Institute of Allergy and Infectious Diseases, Bethesda, Maryland, United States of America.
Brandon J DeKoskyDepartment of Pharmaceutical Chemistry, The University of Kansas, Lawrence, Kansas, United States of America.
John R MascolaVaccine Research Center, National Institute of Allergy and Infectious Diseases, Bethesda, Maryland, United States of America.
John MisasiVaccine Research Center, National Institute of Allergy and Infectious Diseases, Bethesda, Maryland, United States of America.
Nancy J SullivanVaccine Research Center, National Institute of Allergy and Infectious Diseases, Bethesda, Maryland, United States of America.
Tongqing ZhouVaccine Research Center, National Institute of Allergy and Infectious Diseases, Bethesda, Maryland, United States of America.
Peter D KwongVaccine Research Center, National Institute of Allergy and Infectious Diseases, Bethesda, Maryland, United States of America.
National Institute of Allergy and Infectious Diseases · USUniversity of Kansas · USFrederick National Laboratory for Cancer Research · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Since the outbreak of the COVID-19 pandemic, widespread infections have allowed SARS-CoV-2 to evolve in human, leading to the emergence of multiple circulating variants. Some of these variants show increased resistance to vaccines, convalescent plasma, or monoclonal antibodies. In particular, mutations in the SARS-CoV-2 spike have drawn attention. To facilitate the isolation of neutralizing antibodies and the monitoring the vaccine effectiveness against these variants, we designed and produced biotin-labeled molecular probes of variant SARS-CoV-2 spikes and their subdomains, using a structure-based construct design that incorporated an N-terminal purification tag, a specific amino acid sequence for protease cleavage, the variant spike-based region of interest, and a C-terminal sequence targeted by biotin ligase. These probes could be produced by a single step using in-process biotinylation and purification. We characterized the physical properties and antigenicity of these probes, comprising the N-terminal domain (NTD), the receptor-binding domain (RBD), the RBD and subdomain 1 (RBD-SD1), and the prefusion-stabilized spike ectodomain (S2P) with sequences from SARS-CoV-2 variants of concern or of interest, including variants Alpha, Beta, Gamma, Epsilon, Iota, Kappa, Delta, Lambda, Mu, and Omicron. We functionally validated probes by using yeast expressing a panel of nine SARS-CoV-2 spike-binding antibodies and confirmed sorting capabilities of variant probes using yeast displaying libraries of plasma antibodies from COVID-19 convalescent donors. We deposited these constructs to Addgene to enable their dissemination. Overall, this study describes a matrix of SARS-CoV-2 variant molecular probes that allow for assessment of immune responses, identification of serum antibody specificity, and isolation and characterization of neutralizing antibodies.

Identifiers

PMID35018379
PMCPMC8750702
OpenAlexW4206820997

What OpenQuestion holds

Textmetadata
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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.