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猪肺炎支原体P97R1的多克隆抗体制备及亚细胞定位

李欣颖 彭娜娜 于国滨 祝福强 陈玉豪 王洪亮 董伟

动物医学进展2026,Vol.47Issue(6):1-8,8.
动物医学进展2026,Vol.47Issue(6):1-8,8.

猪肺炎支原体P97R1的多克隆抗体制备及亚细胞定位

Preparation of Polyclonal Antibody against Mycoplasma hyopneumoniae P97R1 and Its Subcellular Localization

李欣颖 1彭娜娜 1于国滨 1祝福强 1陈玉豪 1王洪亮 2董伟1

作者信息

  • 1. 湖南农业大学动物医学院,湖南长沙 410128
  • 2. 长沙市动物疫病预防控制中心,湖南长沙 410000
  • 折叠

摘要

Abstract

To explore the biological function of the Mycoplasma hyopneumoniae adhesion factor P97 pro-tein,the P97R1 target gene was synthesized based on the GenBank database,and the prokaryotic expression vector pET28a-P97R1 was constructed.The plasmid was transformed into BL21(DE3)competent cells for protein expression verification.The verified P97R1 protein was mixed with adjuvant to immunize animals and prepare rabbit polyclonal antibodies.The antibody titer and immunogenicity were detected by indirect ELISA.Meanwhile,the physicochemical properties,hydrophobicity,signal peptide,transmembrane region,subcellular localization and secondary structure of the P97R1 protein were analyzed and predicted by bioin-formatics software.In addition,the eukaryotic expression vector pEGFP-N1-P97R1 was constructed.After double enzyme digestion and sequencing verification,it was transiently transfected into HEK293T cells,and the subcellular localization of the P97R1 protein was analyzed by indirect immunofluorescence assay(IFA).The results showed that the molecular weight of the prokaryotic expressed pET28a-P97R1 recombinant protein was approximately 33 ku;indirect ELISA confirmed the successful preparation of rabbit polyclonal antiserum specifically recognizing the P97R1 protein.Bioinformatics analysis predicted that the P97R1 pro-tein was composed of 190 amino acids,with a molecular weight of approximately 17.98 ku,and had no transmembrane region or signal peptide.After the successfully constructed pEGFP-N1-P97R1 eukaryotic vector was transfected into HEK293T cells,IFA confirmed that the P97R1 protein was mainly located in the nucleus.The results indicated that the prokaryotic and eukaryotic expression systems of P97R1 were successfully constructed in this study,and specific polyclonal antibodies were prepared.The nuclear localiza-tion characteristics of the P97R1 protein in eukaryotic cells were also clarified,laying a foundation for in-depth analysis of the biological function of the P97R1 protein and the development of new vaccine strate-gies based on this antigen for porcine mycoplasma pneumonia.

关键词

猪肺炎支原体/P97R1蛋白/多克隆抗体/生物信息学分析/亚细胞定位

Key words

Mycoplasma hyopneumoniae/P97R1 protein/Polyclonal antibody/Bioinformatics analysis/Sub-cellular localization

分类

农业科技

引用本文复制引用

李欣颖,彭娜娜,于国滨,祝福强,陈玉豪,王洪亮,董伟..猪肺炎支原体P97R1的多克隆抗体制备及亚细胞定位[J].动物医学进展,2026,47(6):1-8,8.

基金项目

云南省重大科技专项计划项目(202202AE090032) (202202AE090032)

横向课题(2022xczx-416 ()

2021kjc-js178) ()

动物医学进展

1007-5038

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