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[在北京鉴定出的人博卡病毒衣壳蛋白VP2的表达及在昆虫细胞中病毒样颗粒(VLPs)的形成]

[The expression of the capsid protein VP2 from human bocavirus identified in Beijing and the formation of virus-like particles (VLPs) in insect cells].

作者信息

Zhao Lin-Qing, Qian Yuan, Ding Ya-Xin, Zhu Ru-Nan, Deng Jie, Wang Fang, Sun Yu, Li Yan

机构信息

Laboratory of Virology, Capital Institute of Pediatrics, Beijing 100020, China.

出版信息

Bing Du Xue Bao. 2009 Sep;25(5):333-8.

Abstract

The aim of this study was to obtain the capsid protein VP2 of human bocavirus (HBoV) identified in Beijing recently and construct virus-like particles (VLPs) in insect cells for further study of this virus. The full-length VP2 gene of HBoV from BJ3722 was inserted into the baculovirus expression transfer vector (pFastBac 1) to obtain the recombinant Bacmid, and generation of recombinant baculoviruses was followed by transfection of the recombinant Bacmid into insect cells. Then the recombinant VP2 protein was recognized by SDS-PAGE using Coomassie-blue staining and Western blot using hyper-immune serum against VP2 of HBoV from rabbit. The recombinant baculoviruses were harvested and amplified to gain large amounts of viruses with high titers to infect insect cells at a multiplicity of infection (MOI) of 0. 5. After 7-10 days or 4-5 days of the infection, the supernatants of culture or the cell lysates treated with lysing solution were harvested, and ultracentrifuged twice through 40% sucrose cushion to obtain purified VLPs, which were followed by Western blot and IFA for VLPs' composition and specificity analysis, by electron microscopy for VLPs' morphologic structure. The recombinant VP2 protein with molecular weight of approximately 61 kD expressed in recombinant baculoviruses was recognized by SDS-PAGE using Coomassie-blue staining and Western blot. The presence of VP2 on VLPs was demonstrated by Western blot and IFA from samples collected during the purification of VLPs from the supernatants of culture or the cell lysates, and the expression of VP2 in insect cells led to the formation of VLPs which formed the typical icosahedral appearance of parvoviruses with a diameter of approximately 20 nm. In conclusion, the recombinant baculoviruses were constructed, the HBoV VP2 protein was expressed in insect cells with high specific antigenicity and VLPs was formed successfully.

摘要

本研究旨在获取近期在北京鉴定出的人博卡病毒(HBoV)的衣壳蛋白VP2,并在昆虫细胞中构建病毒样颗粒(VLPs),以便对该病毒进行进一步研究。将来自BJ3722的HBoV全长VP2基因插入杆状病毒表达转移载体(pFastBac 1)中,获得重组杆粒,随后将重组杆粒转染到昆虫细胞中,产生重组杆状病毒。然后,用考马斯亮蓝染色的SDS-PAGE和兔抗HBoV VP2的超免疫血清进行Western blot检测,鉴定重组VP2蛋白。收获重组杆状病毒并进行扩增,以获得大量高滴度的病毒,以感染复数(MOI)为0.5感染昆虫细胞。感染7 - 10天或4 - 5天后,收集培养上清液或用裂解液处理的细胞裂解物,通过40%蔗糖垫层进行两次超速离心,以获得纯化的VLPs,随后通过Western blot和IFA对VLPs的组成和特异性进行分析,通过电子显微镜对VLPs的形态结构进行分析。在重组杆状病毒中表达的分子量约为61 kD的重组VP2蛋白,通过考马斯亮蓝染色的SDS-PAGE和Western blot得到鉴定。通过Western blot和IFA从培养上清液或细胞裂解物中纯化VLPs过程中收集的样品中证实了VLPs上存在VP2,并且VP2在昆虫细胞中的表达导致形成了VLPs,其形成了直径约为20 nm的细小病毒典型二十面体外观。总之,构建了重组杆状病毒,HBoV VP2蛋白在昆虫细胞中高效表达,具有高特异性抗原性,并成功形成了VLPs。

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