Journal of Jilin University(Medicine Edition) ›› 2025, Vol. 51 ›› Issue (6): 1595-1606.doi: 10.13481/j.1671-587X.20250615

• Research in basic medicine • Previous Articles    

Expression purification, antibody preparation, and subcellular localization analysis of Toxoplasma gondii thioredoxin 20

Yuyi SHI1,Shengqi GAN1,Che LIU1,Ziwen CHENG2,Kuo CHENG2,Baoling YANG2,Dawei WANG1()   

  1. 1.Department of Basic Veterinary Medicine,School of Animal Husbandry and Veterinary Medicine,Jinzhou Medical University,Jinzhou 121000,China
    2.Department of Pathogen Biology,School of Basic Medical Sciences,Jinzhou Medical University,Jinzhou 121000,China
  • Received:2024-10-26 Accepted:2025-03-01 Online:2025-11-28 Published:2025-12-15
  • Contact: Dawei WANG E-mail:wangdawei0817@163.com

Abstract:

Objective To express, purify, prepare antibodies, and analyze the subcellular localization of Toxoplasma gondii thioredoxin 20(Trx20), and to provide the reference for the development of Toxoplasma gondii vaccine. Methods Bioinformatics-related websites and software were used to perform bioinformatics analysis of the Trx20 protein; specific primers were designed to amplify the target fragment and construct the prokaryotic expression vector; the protein was expressed in vitro and purified; experimental animals were immunized to prepare antibodies; enzyme-linked immunosorbent assay(ELISA) method was used to detect the titer of the polyclonal antibodies; Western blotting method was used to verify the specificity and sensitivity of the antibodies and to determine the natural expression of the protein; immunofluorescence assay (IFA) was used to analyze the subcellular localization of the protein. Results The bioinformatics analysis results showed that Trx20 protein was a relatively stable hydrophilic protein with a molecular formula of C2172H3412N548O616S20, containing 424 amino acids, a predicted relative molecular mass of 47 700, and a theoretical isoelectric point of 8.55; it was predicted that the protein had one signal peptide, no transmembrane region, contained one domain named “Thioredoxin like Superfamily”, and had 35 phosphorylation sites, one N-glycosylation site, and 17 antigenic determinants; in the secondary structure, alpha-helices accounted for 41.51% of the total amino acids, and random coils accounted for 39.86%; the recombinant plasmids pET-28a-Trx20 and pGEX-4T-1-Trx20 were successfully constructed, and the soluble recombinant protein was expressed and purified; polyclonal antibodies were successfully prepared with a titer as high as 1∶64 000, and they specifically recognized the endogenous Trx20 protein in Toxoplasma gondii; the subcellular localization results showed that Trx20 protein was widely distributed in the cytoplasm of the parasite. Conclusion Toxoplasma gondii Trx20 protein is a secretory protein containing phosphorylation/glycosylation modification sites and a thioredoxin domain, and it is localized in the cytoplasm of the parasite.

Key words: Toxoplasma gondii, Thioredoxin 20, Subcellular localization, Protein purification, Polyclonal antibody

CLC Number: 

  • S855.9