Wang Ru, Wu Minmin, Cai Haijian, An Ran, Chen Ying, Wang Jie, Zhou Nan, Du Jian
Department of Biochemistry and Molecular Biology, School of Basic Medical Sciences, Anhui Medical University, Hefei 230032, China.
Research Center for Infectious Diseases, School of Basic Medical Sciences, Anhui Medical University, Hefei 230032, China.
Trop Med Infect Dis. 2023 Feb 27;8(3):143. doi: 10.3390/tropicalmed8030143.
dense granule protein GRA3 has been shown to promote transmission and proliferation by interacting with the host cell endoplasmic reticulum (ER) through calcium-regulated cyclophilin ligands (CAMLG). Although many studies have focused on the interaction between the host cell endoplasmic reticulum and GRA3, no polyclonal antibodies (PcAbs) against GRA3 have been reported to date. According to the antigenicity prediction and exposure site analysis, three antigen peptide sequences were selected to prepare polyclonal antibodies targeting GRA3. Peptide scans revealed that the major antigenic epitope sequences were ELYDRTDRPGLK, FFRRRPKDGGAG, and NEAGESYSSATSG, respectively. The GRA3 PcAb specifically recognized the GRA3 of type Ⅱ ME49. The development of PcAbs against GRA3 is expected to elucidate the molecular mechanisms by which GRA3 regulates host cell function and contribute to the development of diagnostic and therapeutic strategies for toxoplasmosis.
致密颗粒蛋白GRA3已被证明可通过钙调节亲环蛋白配体(CAMLG)与宿主细胞内质网(ER)相互作用来促进传播和增殖。尽管许多研究集中在宿主细胞内质网与GRA3之间的相互作用,但迄今为止尚未报道针对GRA3的多克隆抗体(PcAb)。根据抗原性预测和暴露位点分析,选择了三个抗原肽序列来制备靶向GRA3的多克隆抗体。肽扫描显示主要抗原表位序列分别为ELYDRTDRPGLK、FFRRRRPKDGGAG和NEAGESYSSATSG。GRA3 PcAb特异性识别Ⅱ型ME49的GRA3。针对GRA3的PcAb的开发有望阐明GRA3调节宿主细胞功能的分子机制,并有助于弓形虫病诊断和治疗策略的开发。