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Expression of human papillomavirus 6b L1 protein in silkworm larvae and enhanced green fluorescent protein displaying on its virus-like particles

机译:人乳头瘤病毒6b L1蛋白在蚕幼虫中的表达及其绿色荧光蛋白在其病毒样颗粒上的展示

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摘要

Human papillomavirus (HPV) 6b L1 capsid protein was expressed using the Bombyx mori nucleopolyhedrovirus (BmNPV) bacmid expression system in silkworm larvae. Two constructs, full-length L1 (500 a.a) and C-terminal-deleted short L1 (479 a.a), and three PCR-manipulated antigenic loops at amino acids 55–56, 174–175, and 348–349 regions were incorporated with whole enhanced green fluorescent protein (EGFP). Expressed in full, short L1 proteins and variants were purified in heparin affinity column chromatography and confirmed by SDS-PAGE and western blot. The presence of self-assembled virus-like particles (VLPs) and EGFP incorporation on the surface of VLPs were confirmed by the observation of transmission electron and immunoelectron microscopies, respectively. HPV 6b L1 major capsid protein was successfully expressed in silkworm, and effective manipulation on the antigenic regions showed the path to versatile vaccine development based on HPV L1-VLPs.
机译:使用家蚕家蚕核多角体病毒(BmNPV)杆粒表达系统在家蚕幼虫中表达人乳头瘤病毒(HPV)6b L1衣壳蛋白。两个构建体,全长L1(500 aa)和C端缺失的短L1(479 aa),以及三个PCR操纵的55-56、174-175和348-349位氨基酸的抗原环整体增强的绿色荧光蛋白(EGFP)。在肝素亲和柱色谱中纯化表达的完整,短L1蛋白和变体,并通过SDS-PAGE和Western blot确认。自组装病毒样颗粒(VLP)和EGFP掺入VLPs表面的情况分别通过观察透射电子和免疫电子显微镜检查得到证实。 HPV 6b L1主要衣壳蛋白已在蚕中成功表达,对抗原区域的有效操作显示了基于HPV L1-VLP的多功能疫苗开发的途径。

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