Evidence map›Paper›PMID 37999620›Full record

ArticleTropical medicine and infectious disease2023

Development of an Optimized Process for Functional Recombinant SARS-CoV-2 Spike S1 Receptor-Binding Domain Protein Produced in the Baculovirus Expression Vector System.

Mohamed Boumaiza, Ameni Chaabene, Ines Akrouti, Meriem Ben Zakour, Hana Askri, Said Salhi, Wafa Ben Hamouda, Soumaya Marzouki, Chaouki Benabdessalem, Melika Ben Ahmed and 2 more

Abstract read
In one paragraph

Article in Tropical medicine and infectious disease, 2023. 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
–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

2 citing papers in PubMed.

  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

12 authors.

Mohamed BoumaizaLaboratory of Molecular Microbiology, Vaccinology and Biotechnology Development, Group of Biotechnology Development, Institut Pasteur de Tunis, Université Tunis El Manar, Tunis 1002, Tunisia.ORCID 0000-0001-7686-6722
Ameni ChaabeneLaboratory of Molecular Microbiology, Vaccinology and Biotechnology Development, Group of Biotechnology Development, Institut Pasteur de Tunis, Université Tunis El Manar, Tunis 1002, Tunisia.
Ines AkroutiLaboratory of Molecular Microbiology, Vaccinology and Biotechnology Development, Group of Biotechnology Development, Institut Pasteur de Tunis, Université Tunis El Manar, Tunis 1002, Tunisia.
Meriem Ben ZakourLaboratory of Molecular Microbiology, Vaccinology and Biotechnology Development, Group of Biotechnology Development, Institut Pasteur de Tunis, Université Tunis El Manar, Tunis 1002, Tunisia.
Hana AskriLaboratory of Molecular Microbiology, Vaccinology and Biotechnology Development, Group of Biotechnology Development, Institut Pasteur de Tunis, Université Tunis El Manar, Tunis 1002, Tunisia.
Said SalhiLaboratory of Molecular Microbiology, Vaccinology and Biotechnology Development, Group of Biotechnology Development, Institut Pasteur de Tunis, Université Tunis El Manar, Tunis 1002, Tunisia.
Wafa Ben HamoudaLaboratory of Transmission, Control and Immunobiology of Infections (LTCII), LR11IPT-02, Institut Pasteur de Tunis, Université Tunis El Manar, 13, Place Pasteur. BP. 74, Tunis 1002, Tunisia.
Soumaya MarzoukiLaboratory of Transmission, Control and Immunobiology of Infections (LTCII), LR11IPT-02, Institut Pasteur de Tunis, Université Tunis El Manar, 13, Place Pasteur. BP. 74, Tunis 1002, Tunisia.ORCID 0000-0002-9882-909X
Chaouki BenabdessalemLaboratory of Transmission, Control and Immunobiology of Infections (LTCII), LR11IPT-02, Institut Pasteur de Tunis, Université Tunis El Manar, 13, Place Pasteur. BP. 74, Tunis 1002, Tunisia.ORCID 0000-0001-7309-6814
Melika Ben AhmedLaboratory of Transmission, Control and Immunobiology of Infections (LTCII), LR11IPT-02, Institut Pasteur de Tunis, Université Tunis El Manar, 13, Place Pasteur. BP. 74, Tunis 1002, Tunisia.ORCID 0000-0002-3179-1648
Khaled TrabelsiLaboratory of Molecular Microbiology, Vaccinology and Biotechnology Development, Group of Biotechnology Development, Institut Pasteur de Tunis, Université Tunis El Manar, Tunis 1002, Tunisia.
Samia RourouLaboratory of Molecular Microbiology, Vaccinology and Biotechnology Development, Group of Biotechnology Development, Institut Pasteur de Tunis, Université Tunis El Manar, Tunis 1002, Tunisia.ORCID 0000-0002-4853-9422

Funding

Ministry of Higher Education and Scientific Research PRFCOVID19-D5P1" registered under the reference 2020/21/I/LR16IPT.
6 · The paper itself

Abstract

To map the spread of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) and evaluate immune response variations against this virus, it is essential to set up efficient serological tests locally. The SARS-CoV-2 immunogenic proteins were very expensive and not affordable for lower- middle-income countries (LMICs). For this purpose, the commonly used antigen, receptor-binding domain (RBD) of spike S1 protein (S1RBD), was produced using the baculovirus expression vector system (BEVS). In the current study, the expression of S1RBD was monitored using Western blot under different culture conditions. Different parameters were studied: the multiplicity of infection (MOI), cell density at infection, and harvest time. Hence, optimal conditions for efficient S1RBD production were identified: MOI 3; cell density at infection 2-3 × 10

Indexed as

cell density at infectionmultiplicity of infectionreceptor-binding domainSARS-CoV-2Sf9 cellsspike S1 glycoprotein

Identifiers

PMID37999620
PMCPMC10674791

What OpenQuestion holds

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Registered trials

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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.