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抗体竞争揭示 HPV L2 次要衣壳蛋白残基 17-36 的表面位置。

Antibody Competition Reveals Surface Location of HPV L2 Minor Capsid Protein Residues 17-36.

机构信息

Department of Microbiology and Immunology, The Pennsylvania State University College of Medicine, Hershey, PA 17033, USA.

Jake Gittlen Laboratories for Cancer Research, The Pennsylvania State University College of Medicine, Hershey, PA 17033, USA.

出版信息

Viruses. 2017 Nov 10;9(11):336. doi: 10.3390/v9110336.

Abstract

The currently available nonavalent human papillomavirus (HPV) vaccine exploits the highly antigenic L1 major capsid protein to promote high-titer neutralizing antibodies, but is limited to the HPV types included in the vaccine since the responses are highly type-specific. The limited cross-protection offered by the L1 virus-like particle (VLP) vaccine warrants further investigation into cross-protective L2 epitopes. The L2 proteins are yet to be fully characterized as to their precise placement in the virion. Adding to the difficulties in localizing L2, studies have suggested that L2 epitopes are not well exposed on the surface of the mature capsid prior to cellular engagement. Using a series of competition assays between previously mapped anti-L1 monoclonal antibodies (mAbs) (H16.V5, H16.U4 and H16.7E) and novel anti-L2 mAbs, we probed the capsid surface for the location of an L2 epitope (aa17-36). The previously characterized L1 epitopes together with our competition data is consistent with a proposed L2 epitope within the canyons of pentavalent capsomers.

摘要

目前可用的九价人乳头瘤病毒(HPV)疫苗利用高度抗原性的 L1 主要衣壳蛋白来促进高滴度中和抗体,但由于反应高度针对特定类型,因此仅限于疫苗中包含的 HPV 类型。L1 病毒样颗粒(VLP)疫苗提供的有限交叉保护需要进一步研究交叉保护的 L2 表位。L2 蛋白在病毒粒子中的精确位置尚未完全确定。除了难以定位 L2 之外,研究还表明,在与细胞结合之前,L2 表位在成熟衣壳的表面上没有很好地暴露。我们使用一系列先前映射的抗 L1 单克隆抗体(mAb)(H16.V5、H16.U4 和 H16.7E)与新型抗 L2 mAb 之间的竞争测定法,探测衣壳表面的 L2 表位(aa17-36)的位置。先前表征的 L1 表位以及我们的竞争数据与五价衣壳子腔中提出的 L2 表位一致。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7add/5707543/95f5ad6bacce/viruses-09-00336-g001.jpg

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