Evidence map›Paper›PMID 42288785›Full record

ArticleBMC biotechnology2026

Rational design and high-yield expression of SARS-CoV-2 nucleocapsid antigen for a sensitive and specific in-house ELISA.

Abbas Tazarghi, Mehdi Behrouzikhah, Hamidreza Abbasi, Mohsen Ebrahimi, Alijan Tabarraei, Ahad Yamchi, Hadi Razavi Nikoo

Abstract read
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Article in BMC biotechnology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Abbas Tazarghi *Department of Microbiology, Faculty of Medicine, Golestan University of Medical Sciences, Gorgan, Iran.
Mehdi Behrouzikhah *Department of Microbiology, Faculty of Medicine, Golestan University of Medical Sciences, Gorgan, Iran.
Hamidreza AbbasiDepartment of Medical Biotechnology, Faculty of Advanced Medical Technologies, Golestan University of Medical Sciences, Gorgan, Iran.
Mohsen EbrahimiNeonatal and Children's Health Research Center, Golestan University of Medical Sciences, Gorgan, Iran.
Alijan TabarraeiDepartment of Microbiology, Faculty of Medicine, Golestan University of Medical Sciences, Gorgan, Iran.
Ahad YamchiDepartment of Biotechnology, Gorgan University of Agricultural Sciences and Natural Resources, Gorgan, Iran. Yamchi@gau.ac.ir.
Hadi Razavi NikooDepartment of Microbiology, Faculty of Medicine, Golestan University of Medical Sciences, Gorgan, Iran. Hadirazavi96@gmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSevere acute respiratory syndrome coronavirus-2 (SARS-CoV-2) is a global pathogen with a high prevalence rate. Among diagnostic methods, serological assays have been effective for rapid screening and identifying a history of infection or vaccination. The nucleocapsid protein is the most conserved and immunogenic antigen of SARS-CoV-2, making it a key target for such tests. Although commercial kits are available for this purpose, a custom design with superior specificity, sensitivity, and accuracy can be both clinically and economically advantageous. In the present study, we designed a recombinant nucleocapsid protein (rNP) using a multi-parameter suite of bioinformatic approaches, including codon optimization, ribosomal binding site engineering, mRNA secondary structure analysis, and optimized expression of the final construct in an E. coli system. The purified rNP was then applied in an in-house ELISA to compare its overall diagnostic efficacy with that of a commercially available kit on a pool of 37 predetermined positive and 15 negative sera for SARS-CoV-2.

resultsResults showed that both assays were 100% specific, but the in-house design showed higher sensitivity (91.9% vs. 83.8%) and a greater area under the curve (0.94 vs. 0.84) compared to the commercial ELISA.

conclusionThis demonstrates that our optimized rNP production platform enables the development of a high-performance serological assay with superior diagnostic accuracy compared to a commercial alternative, providing a powerful and economical tool for surveillance and research in the post-pandemic era.

Indexed as

Antigens, ViralCoronavirus Nucleocapsid ProteinsCOVID-19COVID-19 Serological TestingSARS-CoV-2Antibodies, ViralEnzyme-Linked Immunosorbent AssayEscherichia coliHumansPhosphoproteinsRecombinant ProteinsSensitivity and SpecificityAntibodies, ViralAntigens, ViralCoronavirus Nucleocapsid Proteinsnucleocapsid phosphoprotein, SARS-CoV-2PhosphoproteinsRecombinant ProteinsCodon optimizationDiagnostic assayNucleocapsid proteinRecombinant protein expressionSARS-CoV-2

Identifiers

PMID42288785
PMCPMC13491942

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