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一种特异性识别盖塔病毒E1蛋白线性表位的单克隆抗体的研制。

Development of a monoclonal antibody specifically recognizing a linear epitope on the E1 protein of Getah virus.

作者信息

Liu Muyang, Ren Tongwei, Zhang Liping, Li Peijie, Zhong Zhen, Zhou Lingshan, Qin Yifeng, Ouyang Kang, Chen Ying, Huang Weijian, Wei Zuzhang

机构信息

Laboratory of Animal Infectious Diseases and Molecular Immunology, College of Animal Science and Technology, Guangxi University, Nanning, 530005, China.

Laboratory of Animal Infectious Diseases and Molecular Immunology, College of Animal Science and Technology, Guangxi University, Nanning, 530005, China; Guangxi Zhuang Autonomous Region Engineering Research Center of Veterinary Biologics, Nanning, 530005, China; Guangxi Key Laboratory of Animal Breeding and Disease Control and Prevention, Nanning, 530005, China.

出版信息

Virology. 2025 Jan;602:110315. doi: 10.1016/j.virol.2024.110315. Epub 2024 Nov 26.

Abstract

Getah virus (GETV) is a mosquito-borne alphavirus that can cause disease outbreaks in domesticated mammals. The E1 protein of GETV plays a crucial role in mediating the fusion of viruses and host cells. In this study, the recombinant GETV E1 protein was expressed and administered to BALB/c mice. Hybridoma cells secreting a monoclonal antibody (mAb) 7D4-2 against E1 protein were subsequently obtained using a cell fusion protocol between SP2/0 cells and splenocytes. The reactivity of mAb 7D4-2 with GETV was confirmed through Western blot analysis and indirect immunofluorescence assay (IFA). A precise B cell linear epitope, 281-DIPDTAF-287, was identified using Western blot analysis with the produced mAb 7D4-2 by constructing and expressing a series of truncated His-fused E1 proteins. Conservation analysis indicated that this epitope is highly conserved in Group III strains of GETV, but exhibits an amino acid difference (T285S) compared to Group I, Group II, and Group IV. Cross-reactivity analysis by Western blot demonstrated that the B-cell epitope containing the mutation could be recognized by mAb 7D4-2. The ability of mAb 7D4-2 to recognize the epitope carrying the T285S mutation was further confirmed using an infectious clone of GETV. This study enhances the understanding of the biological characteristics of the E1 protein and will facilitate the future development of diagnostic tests for GETV.

摘要

盖塔病毒(GETV)是一种由蚊子传播的甲病毒,可在驯养哺乳动物中引发疾病爆发。GETV的E1蛋白在介导病毒与宿主细胞融合过程中起关键作用。在本研究中,表达了重组GETV E1蛋白并将其注射给BALB/c小鼠。随后,通过SP2/0细胞与脾细胞之间的细胞融合方案,获得了分泌针对E1蛋白的单克隆抗体(mAb)7D4-2的杂交瘤细胞。通过蛋白质免疫印迹分析和间接免疫荧光测定(IFA)证实了mAb 7D4-2与GETV的反应性。通过构建和表达一系列截短的His融合E1蛋白,使用产生的mAb 7D4-2进行蛋白质免疫印迹分析,鉴定出一个精确的B细胞线性表位281-DIPDTAF-287。保守性分析表明,该表位在GETV的III组毒株中高度保守,但与I组、II组和IV组相比存在氨基酸差异(T285S)。蛋白质免疫印迹交叉反应分析表明,含有该突变的B细胞表位可被mAb 7D4-2识别。使用GETV的感染性克隆进一步证实了mAb 7D4-2识别携带T285S突变表位的能力。本研究增进了对E1蛋白生物学特性的理解,并将有助于未来开发GETV诊断检测方法。

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