[Preparation of mouse monoclonal antibodies against human adenovirus 55 Hexon (HAdV55 Hexon) protein].

Ruodong Yuan, Yangchao Dong, Fuxing Wu, Tian Duan, Pan Xue, Jian Zhang, Mingcheng Yuan, Zhifeng Xue, Haijun Zhang, Qianqian Zhang, Xiaopeng Gao, Yingfeng Lei
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Abstract

Objective To prepare specific mouse monoclonal antibody (mAb) against human adenovirus type 55 Hexon protein (HAdV55 Hexon). Methods The Hexon genes of HAdV55, 3, 4, 7, 16 and 21 were chemically synthesized as templates for PCR amplification. The prokaryotic expression plasmids pET28a-HAdV55 Hexon and eukaryotic expression plasmids pCAGGS-HAdV3, 4, 7, 16, 21 and 55 Hexon were constructed respectively. The pET28a-HAdV55 Hexon plasmid was transformed into E. coli competent cell BL21 (DE3) and was induced by IPTG. After the purified inclusion body was denatured and renatured, Hexon55 protein was purified by tangential flow filtration system. pCAGGS-HAdV55 Hexon was used to immunize BALB/c mice by cupping, and HAdV55 Hexon protein was used to booster immunization. The anti-HAdV55 Hexon mAb was prepared by hybridoma technique and the titer and subclass were determined. The specificity of antibody was identified by Western blot using HEK293T cells transfected with pCAGGS-HAdV55 Hexon and by immunofluorescence assay (IFA) using BHK cells transfected with pCAGGS-HAdV55 Hexon. Both clones with high titer were selected, and the cross-reactivity of pCAGGS-HAdV3, 4, 7, 16, 21 and 55 Hexon transfected cells were analyzed by Western blot analysis and IFA. Results PET28a-HAdV55 Hexon and pCAGGS-HAdV55 Hexon, 3, 4, 7, 16 and 21 expression plasmids were successfully constructed. BL21 transformed with pET28a-HAdV55 Hexon was induced by IPTG. The HAdV55 Hexon protein was mainly expressed in the form of inclusion body. After denaturation and renaturation, the purified HAdV55 Hexon protein was obtained by ultrafiltration. Six hybridoma cell lines secreting HAdV55 Hexon mAb were obtained. The antibody subclass analysis showed that 2 strains were IgG2a subtypes and 4 strains were IgG2b. Two specific HAdV55 Hexon antibodies with high titer were obtained, and there was no cross-reactivity with HAdV3, 4, 7, 16, 21 Hexon. Conclusion The specific mice mAb against HAdV55 Hexon provides an experimental basis for establishing its antigen detection method.

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人腺病毒55 Hexon (HAdV55 Hexon)蛋白小鼠单克隆抗体的制备
目的制备抗人腺病毒55型Hexon蛋白(HAdV55 Hexon)特异性小鼠单克隆抗体(mAb)。方法化学合成HAdV55、3、4、7、16、21 Hexon基因作为PCR扩增模板。分别构建原核表达质粒pET28a-HAdV55 Hexon和真核表达质粒pCAGGS-HAdV3、4、7、16、21和55 Hexon。将pET28a-HAdV55 Hexon质粒转入大肠杆菌感受态细胞BL21 (DE3),经IPTG诱导。将纯化的包涵体变性、再变性后,用切向流过滤系统纯化Hexon55蛋白。采用pCAGGS-HAdV55 Hexon对BALB/c小鼠拔罐免疫,采用HAdV55 Hexon蛋白加强免疫。采用杂交瘤技术制备抗hadv55 Hexon单抗,测定其效价和亚类。转染pCAGGS-HAdV55 Hexon的HEK293T细胞和转染pCAGGS-HAdV55 Hexon的BHK细胞分别采用Western blot和免疫荧光法(IFA)鉴定抗体的特异性。选择两个高滴度的克隆,采用Western blot和IFA分析转染pCAGGS-HAdV3、4、7、16、21和55 Hexon细胞的交叉反应性。结果成功构建了PET28a-HAdV55 Hexon和pCAGGS-HAdV55 Hexon、3、4、7、16和21个表达质粒。转染pET28a-HAdV55 Hexon的BL21用IPTG诱导。HAdV55 Hexon蛋白主要以包涵体的形式表达。经过变性和再变性后,通过超滤得到纯化的HAdV55 Hexon蛋白。获得6株分泌HAdV55 Hexon mAb的杂交瘤细胞株。抗体亚类分析显示2株为IgG2a亚型,4株为IgG2b亚型。获得两种特异性高效价的HAdV55 Hexon抗体,与HAdV3、4、7、16、21 Hexon无交叉反应。结论HAdV55 Hexon特异性小鼠单抗为建立HAdV55 Hexon抗原检测方法提供了实验依据。
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