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荧光乳头瘤病毒样颗粒的构建与生产。

Construction and production of fluorescent papillomavirus-like particles.

作者信息

Peng S, Zhou J, Frazer I H

机构信息

Department of Pediatrics, Xiehe Hospital, Tongji Medical University, Wuhan 430022.

出版信息

J Tongji Med Univ. 1999;19(3):170-4, 180. doi: 10.1007/BF02887727.

Abstract

The green fluorescent protein (GFP) from the jellyfish Aequorea victoria has attracted widespread interest since it was demonstrated to be fluorescent in vivo when expressed in other organisms. In order to investigate papillomavirus life cycle which hampered by the unavailability of conventional cell culture system, we constructed a chimeric bovine papillomavirus (BPV) type 1 virus-like particles (VLPs) containing GFP. It was found that fluorescent VLPs could be assembled from L2 protein in which GFP is inserted into the N-terminal region of L2 (aa 88). The fluorescent VLPs could also be assembled from a GFP/L2 fusion protein in which part of the L2 sequence had been deleted. In vitro, fluorescent VLPs could bind to CV-1 cells, and this VLP/cell interaction could be analyzed by FACS assay. These results demonstrated that GFP could incorporate into BPV1 VLPs without disruption of the VLP structure. Fluorescent VLPs might be a useful tool for study of papillomavirus virus/cell interaction.

摘要

自维多利亚多管水母的绿色荧光蛋白(GFP)在其他生物体中表达时被证明在体内具有荧光以来,它引起了广泛关注。为了研究因缺乏传统细胞培养系统而受阻的乳头瘤病毒生命周期,我们构建了一种包含GFP的嵌合牛乳头瘤病毒1型病毒样颗粒(VLP)。发现荧光VLP可以由将GFP插入L2(第88位氨基酸)N端区域的L2蛋白组装而成。荧光VLP也可以由缺失部分L2序列的GFP/L2融合蛋白组装而成。在体外,荧光VLP可以与CV-1细胞结合,并且这种VLP/细胞相互作用可以通过流式细胞术分析。这些结果表明GFP可以掺入BPV1 VLP中而不破坏VLP结构。荧光VLP可能是研究乳头瘤病毒病毒/细胞相互作用的有用工具。

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