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利用单克隆抗体鉴定牛乳头瘤病毒1型的L2开放阅读框基因产物

Identification of L2 open reading frame gene products of bovine papillomavirus type 1 using monoclonal antibodies.

作者信息

Jin X W, Cowsert L M, Pilacinski W P, Jenson A B

机构信息

Department of Pathology, Georgetown University School of Medicine, Washington, D.C. 20007.

出版信息

J Gen Virol. 1989 May;70 ( Pt 5):1133-40. doi: 10.1099/0022-1317-70-5-1133.

Abstract

Four hybridoma cell lines producing monoclonal antibodies (MAbs) to bovine papillomavirus type 1 (BPV-1) L2 open reading frame (ORF) gene products have been established from mice immunized with a BPV-1 L2-beta-galactosidase fusion protein. Hybridomas were selected and cloned (from over 700 hybridomas) on the basis of specific reactivity of supernatant fluids with BPV-1 L2 epitopes on disrupted BPV-1 particles and L2-beta-galactosidase fusion proteins by ELISA and Western blotting, and with acetone-fixed frozen sections of BPV-1-induced fibropapillomas by immunofluorescence. These MAbs were not reactive with intact BPV-1 particles or BPV-1 L1-beta-galactosidase fusion proteins by ELISA or with beta-galactosidase by ELISA and Western blotting. The four MAbs detected viral structural proteins of Mr 76K, 68K and possibly 55K in purified BPV-1 preparations by Western blotting. Two of the four MAbs were cross-reactive with BPV-2-induced fibropapillomas. These findings suggest that (i) the BPV-1 L2 ORF encodes the minor capsid protein(s), (ii) the gene products of the BPV-1 L2 ORF have Mr values of 76K, 68K and possibly 55K, (iii) minor capsid epitopes are internal to the BPV-1 particle, and (iv) MAbs reactive with genetically engineered truncated BPV-1 L2 ORF gene products can distinguish between BPV-1 and BPV-2 productive infections.

摘要

用牛乳头瘤病毒1型(BPV-1)L2开放阅读框(ORF)基因产物免疫小鼠后,已建立了4株产生针对BPV-1单克隆抗体(MAb)的杂交瘤细胞系。通过ELISA和蛋白质印迹法,根据上清液与破碎的BPV-1颗粒上的BPV-1 L2表位以及L2-β-半乳糖苷酶融合蛋白的特异性反应性,以及通过免疫荧光法与BPV-1诱导的纤维乳头瘤的丙酮固定冰冻切片的反应性,从700多个杂交瘤中筛选并克隆出杂交瘤。通过ELISA,这些单克隆抗体与完整的BPV-1颗粒或BPV-1 L1-β-半乳糖苷酶融合蛋白无反应,通过ELISA和蛋白质印迹法与β-半乳糖苷酶无反应。通过蛋白质印迹法,这4种单克隆抗体在纯化的BPV-1制剂中检测到分子量为76K、68K以及可能为55K的病毒结构蛋白。这4种单克隆抗体中有2种与BPV-2诱导的纤维乳头瘤有交叉反应。这些发现表明:(i)BPV-1 L2 ORF编码次要衣壳蛋白;(ii)BPV-1 L2 ORF的基因产物分子量为76K、68K以及可能为55K;(iii)次要衣壳表位在BPV-1颗粒内部;(iv)与基因工程截短的BPV-1 L2 ORF基因产物反应的单克隆抗体可区分BPV-1和BPV-2的生产性感染。

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