{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,6]],"date-time":"2026-10-06T20:55:34Z","timestamp":1791320134007,"version":"4.3.1"},"reference-count":66,"publisher":"Springer Science and Business Media LLC","issue":"2","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2018,6,26]]},"abstract":"<jats:title>Abstract<\/jats:title>\n<jats:p><jats:italic>Toxoplasma gondii<\/jats:italic> infects almost all the warm-blooded animals. ROP20 protein is expressed in the rhoptry of <jats:italic>Toxoplasma gondii<\/jats:italic>. In this study, the secondary structure of ROP20 was analyzed using SMART software. We constructed and analyzed the 3D model of ROP20 protein using SWISS-MODEL online procedure and Visual Molecular Dynamics (VMD) software. The structure analysis fully indicated that ROP20 protein is an important member of the ROP family. Furthermore, We used DNASTAR software and Epitope Database online service to analyze liner-B cell epitopes and T-cell epitopes of ROP20 protein. All the analysis results of ROP20 protein can provide positive information on treatment and vaccine for toxoplasmosis. Moreover, ROP20 gene was obtained from PCR, and a recombinant eukaryotic expression vector (pEGFP-C1-ROP20) was constructed in the following study. After restriction enzyme digestion, the constructed plasmid was transfected into HEK 293-T cells. The RT-PCR result indicated that the recombinant plasmid could transcribe successfully in HEK 293-T cell. The results of western blotting indicated the expressed proteins can be recognized by anti-STAg mouse sera.<\/jats:p>","DOI":"10.1515\/ap-2018-0028","type":"journal-article","created":{"date-parts":[[2018,4,14]],"date-time":"2018-04-14T22:16:02Z","timestamp":1523744162000},"page":"244-251","source":"Crossref","is-referenced-by-count":11,"title":["Structural predication and antigenic analysis of Toxoplasma gondii 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