CAJ | 학술논문

目的表达具有免疫学活性重组F1抗原(rF1),并以其构建检测鼠疫抗体胶体金试纸条.方法将去掉信号肽编码序列的caf1基因片段与载体质粒pET32a(+)通过BamHI和Not I双酶切位点进行连接,将重组质粒[caf1-pET32a(+)]转化入BL21(DE3)中进行诱导表达,表达产物经亲和层析纯化,以纯化rF1及天然F1抗原制备双检测鼠疫抗体胶体金标试纸条,并对浙江省528份人血清标本进行检测.结果含caf1-pET32a(+)的BL21(DE3),经诱导产生相对分子质量(M_r)约为35.5×10~3的rF1融合蛋白;rF1融合蛋白检测鼠疫抗体的敏感性等同甚至超越天然F1抗原;在528份人血清标本的检测中,rF1与天然F1的符合率为97.9%(K=0.466),有较好一致性.结论制备的rF1,具有良好免疫学活性,该rF1可替代天然F1抗原,用于鼠疫免疫学检测.
목적 표체구유면역학활성중조F1항원(rF1),병이기구건검측서역항체효체금시지조.방법 장거도신호태편마서렬적caf1기인편단여재체질립pET32a(+)통과BamHI화Not I쌍매절위점진행련접,장중조질립[caf1-pET32a(+)]전화입BL21(DE3)중진행유도표체,표체산물경친화층석순화,이순화rF1급천연F1항원제비쌍검측서역항체효체금표시지조,병대절강성528빈인혈청표본진행검측.결과함caf1-pET32a(+)적BL21(DE3),경유도산생상대분자질량(M_r)약위35.5×10~3적rF1융합단백;rF1융합단백검측서역항체적민감성등동심지초월천연F1항원;재528빈인혈청표본적검측중,rF1여천연F1적부합솔위97.9%(K=0.466),유교호일치성.결론 제비적rF1,구유량호면역학활성,해rF1가체대천연F1항원,용우서역면역학검측.
Objective To get recombinant F1 antigen (rF1) and to construct the detection dipstick of plague antibody. Methods The cafl gene removing the signal peptide coding sequence was cloned into plasmid pET32a ( +) by double-digested sites of BamHI and Not I. Recombinant plasmid caf1-pET32a(+) was transformed into BL21 (DE3) and the rFl was expressed. Expression products were purified by affinity chromatography. Dual detection dipstick of plague antibody was constructed with purified rF1 and natural F1, and evaluated with 528 human serum samples of Zhejiang province. Results The fusion protein rF1 of 35.5 KD was expressed by BL21 strains containing caf1-pET32a( + ). The sensitivity of rF1 showed equivalent to or higher than the natural Fl antigen in detecting plague antibody. It seemed that there was a better consistency of 97.9% (k= 0.466) when 528 human sera was detected by rF1 and natural F1. Conclusion We successfully extracted the rF1 with good immunological activity that might be used to detecting Yersinia pestis.