eng Djukić, Teodora Ćirković Veličković, Tanja Radomirović, Mirjana Simović, Ana Vasović, Tamara Ćujić, Danica Dević, Marija Sabljić, Ljiljana Smiljanić, Katarina Radosavljević, Jelena Stanić-Vučinić, Dragana Mladenović, Maja info:eu-repo/semantics/article https://phaidrabg.bg.ac.rs/o:25895 doi:10.1016/j.virol.2021.01.004 ABSTRACT Serological testing is important method for diagnosis of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection. Nucleocapsid (N) protein is the most abundant virus derived protein and strong immunogen. We aimed to find its efficient, low-cost production. SARS-CoV-2 recombinant fragment of nucleocapsid protein (rfNP; 58–419 aa) was expressed in E. coli in soluble form, purified and characterized biochemically and immunologically. Purified rfNP has secondary structure of full-length recombinant N protein, with high percentage of disordered structure (34.2%) and of β-sheet (40.7%). rfNP was tested in immunoblot using sera of COVID-19 convalescent patients. ELISA was optimized with sera of RT-PCR confirmed positive symptomatic patients and healthy individuals. IgG detection sensitivity was 96% (47/50) and specificity 97 (67/68), while IgM detection was slightly lower (94% and 96.5%, respectively). Cost-effective approach for soluble recombinant N protein fragment production was developed, with reliable IgG and IgM antibodies detection of SARS-CoV-2 infection. Expression, purification and immunological characterization of recombinant nucleocapsid protein fragment from SARS-CoV-2 Elsevier application/pdf 3913496 bytes All rights reserved recombinant nucleocapsid protein, COVID-19, SARS-CoV-2, prokaryotic expression, serological assay Virology 557 2021